My client based in the south west is looking for a Pharmacist to work within the

Sat, 22 Nov 2008 09:08:31 GMT

dispensary, you will also have screening experience aswell. Accommodation is a possibility for this position.. £29.00 - Contact seller

Fantastic office-based Senior Clinical Research Associate (SCRA) career

Sat, 22 Nov 2008 09:08:31 GMT

opportunity. Previous EU monitoring experience is a must have, ideally in Belgium, Germany, Spain or France. Our client is a sought-after technology-driven, global health care company specialised in pharmaceutical products (neurology, dermatology, eye care, etc) with approximately 5,000 employees worldwide. The Role and your Responsibilities You will be responsible for the monitoring of studies across different therapeutic areas for pan-European and International that are performed in the UK and in Europe. The ideal Senior Clinical Research Associate (SCRA) is required to provide study management and central co-ordination of the monitoring function from feasibility to study completion, across all regions, phases and therapy areas. The ideal Senior Clinical Research Associate (SCRA) will act as the Site Expert supporting the trial team relating to the conduct of all Clinical Development activities and overseeing CRO activity in outsourced clinical trials in their assigned countries. The ideal Senior Clinical Research Associate (SCRA) will have previous clinical study and clinical project experience as this will be part of your responsibilities. What is Required PhD / MSc / Pharm D or BSc with relevant clinical research experience. European/International clinical monitoring experience in at least 2 European countries is essential Fluency in written and spoken English. Broad therapeutic knowledge with an emphasis on Neurology Clinical understanding and experience of the different legal interpretations in the EU member states around the same EU regulations. Knowledge of appropriate EU Pharmaceutical legislation e. g. Clinical Trial and GCP Directives, ICH GCP guidelines. What is Offered Office-based 5 days a week; Companys office in Buckinghamshire (Bucks); Permanent position with a salary ranging from £35,000 per annum to £37,000 per annum, depending on level of skills and experience; Competitive company package (10% bonus at target, car allowance or company car, etc); January 2009 start date, ideally. Please send your CV to find out more about this excellent contract opportunity!. £37,000.00 - Contact seller

My client based in London is looking for Production Pharmacist to start

Sat, 22 Nov 2008 09:08:31 GMT

immediatley and the position is ffor the next three months. You must have at least twelve months experience within Production.. £35.00 - Contact seller

Medacs International Plc We are one of the largest suppliers of healthcare

Sat, 22 Nov 2008 09:08:31 GMT

professionals in the UK. This provides us with more resources and a larger coverage and knowledge of the healthcare market. Being market leaders in the industry we have the know-how and experience to be equipped to understand your job requirements as a healthcare professional and finding you the perfect role. Community Pharmacist A number of positions have become available across Greater London for Community Pharmacists who have had previous experience. You must be registered with the HPC. All applications will be treated with the strictest of confidence. We have a variety of positions ranging from locum to contract or permanent work. On top of this we offer competitive pay rates, daily payroll and other benefits respective with experience. If you think this may be for you, or to find out further information please contactone of our consultantsat Medacs International Plc to discuss up coming opportunities. Click Apply Now!. £0.00 - Contact seller

We are looking for a Medical Scientific Liaison manager to work within a

Sat, 22 Nov 2008 09:08:31 GMT

pharmaceutical company. The successful person would be working at a high level within the NHS, liaising and educating the consultants, key decision makers and Kep Opinion Leaders with regards to the products the company supplies. You will:--position theproduct portfolio (current and future)within relevant national and regional guidelines to enable the sales and marketing teams to maximise business. -Leverage Key Opinion Leaders (in conjunction with Medical, Marketing and Sales (MMS) to positively influence future guidelines/ funding/ positioning of in-market and pre-market products/ devices -Help devise and develop financial impact models, market access programmes, hospital experience programmes (in conjunction with MMS) to improve and advance the usage of the product portfolioYou will report directly into the Medical Director and you must have a good clinical understanding as well as an understanding of the pharmaceutical industry. This is a very exciting and heavy weight job that brings with it fantastic rewards. If interested then please contact us immediately as they are looking to recruit imminently. ** DON'T MISS THIS FANTASTIC OPPORTUNITY! ** ** Applications only from those eligible to work within the European Union *. £50,000.00 - Contact seller

Fantastic home-based/field-based career opportunity for CRAs (Clinical Research

Sat, 22 Nov 2008 09:08:31 GMT

Associates) with previous UK clinical monitoring experience. Great team and great clinical studies! Experienced CRAs (Clinical Research Associates) urgently required to provide clinical monitoring. Our client is a leader in its field with over 500 staff in the UK and has a truly global international development programme. They have a very strong pipeline with expertise across several therapeutic areas. They are now recruiting a field-based CRA to join their team based in the UK. The Role and your Responsibilities The field-based CRA (Clinical Research Associate) will be part of a dynamic team with a big pipeline working on a mix of therapeutic areas, monitoring sites UK-wide. The team provides a lot of support and training to their clinical research staff. They also have an in-house department looking after the ethics, site contracts further supporting their CRAs. This role will require to perform UK-wide monitoring visits though some regionalized monitoring can sometime be offered. What is Required Previous clinical monitoring experience in the UK, preferably Previous work experience as a CRA (Clinical Research Associate) Proven clinical experience across several therapeutic areas, Oncology preferred though not essential. Willingness to travel 50-60% of the time Full driving licence Candidates must be eligible to work in UK. What is Offered Field-based position Excellent support and training opportunities Dynamic friendly team Company's offices are based in Cambridgeshire, Permanent contract competitive package & great benefits, seconded to our client on a 12-month renewable contract basis December 2008 January 2009 ideal start date Please send your CV today to find out more about this fantastic career opportunity.. £27,000.00 - Contact seller

My client based on the south coast is looking for a Pharmacist to start asap for

Sat, 22 Nov 2008 09:08:31 GMT

the next few months. You musthave ward and dispensary experience and be able to go straight in and not require much training within this large pharmacy department. Accommodation is possibly available for this position.. £30.00 - Contact seller

My client a large hospital based in the North West is looking for a Pharmacist

Sat, 22 Nov 2008 09:08:31 GMT

who has experience within dispensary and clinical. Accommodation can be provided for this position.. £29.00 - Contact seller

** SPECIALITY PHARMA COMPANY REQUIRES EXPERIENCED MEDICAL SCIENCE LIASON

Sat, 22 Nov 2008 09:08:31 GMT

MANAGER**My client, a specialty pharmaceutical company, requires an ambitious Medical Science Liaison Manager. With a strong and growing portfolio of specialised hospital medicines focused on oncology, pain control and critical care, they are searching for an experienced, professional to share in their future success. The successful candidate will report into the medical director and cover the whole of the UK (covering 22 specific units), liaising with Senior influential consultants and key opinion leaders with the NHS and hospitals. You will hold a PhD or equivalent qualification and have previous knowledge and experience of the clinical industry. You will demonstrate effective presentation, negotiation and time management skills and possess the ability to work independently, managing competing priorities. You will also be highly customer focused and a strong team player. This is an unmissable opportunity to work for a rapidly growing company with a fantastic reputation within the Clinical Industry. ** DON'T MISS THIS FANTASTIC OPPORTUNITY! ** ** Applications only from those eligible to work within the European Union *. £0.00 - Contact seller

Pharmacy UK - Pharmacist - EastbourneSimply Health Pharmacy are currently

Fri, 21 Nov 2008 07:18:56 GMT

recruiting for a highly motivated and enthusiastic Pharmacist, who thrives on providing outstanding patient care, you will be required to deliver a pharmacy service that complies with the code of ethics, professional standards and relevant legislation. Providing a pharmacy service - meeting and exceeding customer expectation. Maximising and driving profitable OTC sales, pharmacy items and near patient services. If you have just completed your Pre Registration year and are looking for the next move, then this is a great opportunity for you. You will be registered as a pharmacist with the Royal Pharmaceutical Society of Great Britain (RPSGB) £ excellent + benefits inc If you wish to apply for the position then please forward your CV or contact Phyllis Sherriff.. £0.00 - Contact seller

Pharmacy UK - Pharmacy Manager - EastbourneSimply Health Pharmacy has an

Fri, 21 Nov 2008 07:18:56 GMT

exciting challenge for an Experienced Pharmacy Manager who is passionate about Retail Management and wants to push forward a pharmacy commercially. Key areas of responsibility include: Staff management Dispensing medicines Patient education and counseling OTC counseling and advice Communicating with doctors and nurses Stock order and control You will need at least 2 years experience working as a Supervising Pharmacist. You will be registered Pharmacist. This excellent opportunity will come with an Excellent Salary Package along with Bonus and other benefits. If you wish to apply for the position then please forward your CV or contact Phyllis Sherriff.. £0.00 - Contact seller

Pharmacy UK - Pharmacist - MaidstoneSimply Health Pharmacy are currently

Fri, 21 Nov 2008 07:18:56 GMT

Pharmacy UK - Pharmacy Manager - MaidstoneSimply Health Pharmacy has an exciting

Fri, 21 Nov 2008 07:18:56 GMT

challenge for an Experienced Pharmacy Manager who is passionate about Retail Management and wants to push forward a pharmacy commercially. Key areas of responsibility include: Staff management Dispensing medicines Patient education and counseling OTC counseling and advice Communicating with doctors and nurses Stock order and control You will need at least 2 years experience working as a Supervising Pharmacist. You will be registered Pharmacist. This excellent opportunity will come with an Excellent Salary Package along with Bonus and other benefits. If you wish to apply for the position then please forward your CV or contact Phyllis Sherriff.. £0.00 - Contact seller

Pharmacy UK - Pharmacist - CoventrySimply Health Pharmacy are currently

Fri, 21 Nov 2008 07:18:56 GMT

Pharmacy UK - Pharmacy Manager - CoventrySimply Health Pharmacy has an exciting

Fri, 21 Nov 2008 07:18:56 GMT

Pharmacy UK - Pharmacy Manager - SheffieldSimply Health Pharmacy has an exciting

Fri, 21 Nov 2008 07:18:56 GMT

Commissioning Manager - £45,000 - £50,000 - Various locations
Fri, 21 Nov 2008 07:18:56 GMT
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This dynamic organisation with a forward thinking and flexible business strategy are looking for an experienced Commissioning Manager to join their established team.

Job Title:Commissioning Manager
Salary:£45,000 - £50,000
Location:Various locations

Operating as commissioning manager within this pharmaceutical and healthcare company you will have experience of high value relationships and will feel equally comfortable with the challenges of key account management and business development. With a track record in a role of similar responsibility working with the NHS, preferably relating to pathology this role will be the fresh challenge you have been looking for.

This is a unique opportunity to join an organisation where you can take an active part in the future success of the company. You will rewarded for your success and will be offered a progressive career path to match your ambition and drive.

Offering your strategic thinking to this diverse role, you are a strong communicator with first class relationship management skills and the enthusiasm to rise to a challenge. Working closely with your clients and internal teams, customer focus is paramount to your work ethics as is your strong influencing skills which offer mutual benefits.

Profile:Experience of key account management and business development
Experience of a high profile role with the NHS, preferably in pathology
Strong influencing skills and relationship management abilities
A positive attitude and a willingness to rise to new challenges

Please note that our client can only consider candidates who are authorised to work in the UK.. £50,000.00 - Contact seller

Pharmacy Manager (Alternative Therapy) required for a pharmaceutical company

Fri, 21 Nov 2008 07:18:56 GMT

based in St. AlbanDuties and responsibilities to develop, direct, maintain, and evaluate pharmaceutical services in our alternative therapy department; forecasts, develops, and manages the departmental and legal requirements of pharmacy practice; plans, assigns, and reviews work of assigned staff, maximise staff effectiveness through training and development; supervises the procurement, storing, and accounting of pharmaceuticals; provides consultation on pharmaceutical questions to physicians, residents, nurses, and other health care providers. Applicants must have degree level qualification with relevant experience. Closing Date: 26/11/2008. £34,000.00 - Contact seller

Pharmacy UK - Pharmacy Manager - BrightonSimply Health Pharmacy has an exciting

Fri, 21 Nov 2008 07:18:55 GMT

Pharmacy UK - Pharmacist - BrightonSimply Health Pharmacy are currently

Fri, 21 Nov 2008 07:18:55 GMT

Job DescriptionWe are looking for a Pharmacist who has experience in dispensary

Fri, 21 Nov 2008 07:18:55 GMT

. Ideally a Grade C or D but all Grades will be consideredTo start asap (or end of November) til the end of FebruaryBased in Glasgow CityCompetitive rates depending on P. A. Y. E or Limited CompanyMust be registered with RPSGBRefer a friend and receive a one off payment.. £0.00 - Contact seller

In the current health care environment the registration of new drugs is an

Fri, 21 Nov 2008 07:18:55 GMT

important step into the market. Increasingly, additional information in terms of clinical and economic value is required to provide convincing Health Economics arguments for pricing, reimbursement and marketing purposes. In times of parallel processing of information for registration and publication, under tight timelines,My Clientrealises the need for dedicated resources to provide statistical, scientific & strategic expertise to HE&OR for the generation of evidence for payers. Therefore, within the department of Clinical Information, they are building a group to collaborate with the global Health Economics and Outcomes Research (HE&OR) function. The main task of this group is to influence the design of clinical development projects and studies to include the important aspects of HE&OR support, to plan and implement the analysis and reporting of relevant endpoints, and to support the publications in this area. This group should also function as a center of excellence and as advocates for theses aspects within the various functions of Clinical Research and Development in the company. Working as part of one of the leading Biostatistics groups in the pharmaceutical industry, you are part of an exciting environment, driven by innovation and cutting edge methodology and offering a wealth of development opportunities. Requirements University degree in Statistics or Mathematics or a related area (Ph. D. or MSc. level) At least seven years relevant experience in the field of clinical trials for a senior level position, or at least three years for a more junior level as a must, preferably with experience in the HE&OR area. Good knowledge of clinical trials methodology, scientific computation and SAS; S-Plus an advantage. Flexible, positive, creative thinker, good communicator, negotiator and team player. £0.00 - Contact seller

The Therapeutic Area Statistician is responsible for all statistical aspects of

Fri, 21 Nov 2008 07:18:55 GMT

individual clinical trials. Major Activities are to be responsible for all statistical tasks on the assigned clinical trials, e. g. , clinical trial design/planning, analysis plan, reporting activities, exploratory analyses and additional analyses to support publications, and statistical consultation during the running phase; Track clinical trial activities and milestones; Ensure timeliness and adequate quality of all CIS deliverables for the assigned trials; Follow processes and adhere tomy Client'sand project specific standards as well as Health Authority requirements (SOPs, NIPs, Master Analysis Plan, GCP, and regulatory guidelines); Establish and maintain sound working relationships and effective communication within the clinical trial team and the CIS team; Participate in non-clinical project activities as needed. Requirements At least Masters Degree in Statistics (or equivalent degree). Fluent English (oral and written) No specific previous job experience required for a Ph. D. For holders of a Masters Degree, 2 years relevant experience is required. Knowledge and expertise in Statistics. Knowledge of statistical software packages.. £0.00 - Contact seller

Responsible for all statistical tasks on the assigned clinical trials; May be

Fri, 21 Nov 2008 07:18:55 GMT

assigned to lead a small project or parts (e. g. indication); Track clinical trial/allocated project activities and milestones; Ensure timeliness and adequate quality of all deliverables for the assigned trials and project tasks; Follow processes and adhere to my Client's and project specific standards as well as Health Authority requirements (SOPs, Master Analysis Plan, GCP, and regulatory guidelines); Participate in or lead non-clinical project activities as needed; Establish and maintain sound working relationships and effective communication within the Clinical Trial Team/International Clinical Team and the Biostatistics team. Requirements At least Masters Degree in Statistics (or equivalent degree) with 5 years of experience or PhD with 2-3 years of experience. Fluent English (oral or written). Experience in all tasks of a Trial Statistician. Proven knowledge in Statistics and its applications to clinical trials. Proven knowledge of drug development and HA guidelines. Background medical knowledge, preferably in relation to the specific therapeutic area. Proven knowledge of statistical software packages. Good communication and presentation skills. Good team player.. £0.00 - Contact seller

Scientific and operational management of parts of a portfolio of projects, in

Fri, 21 Nov 2008 07:18:55 GMT

some cases globally; Ensure high quality contributions to drug development and commercialisation in the TA area, including implementation of innovative methods; Contribute to the development of the B&SR organisation through his/her leadership role on the management team; Efficient resource management within his/her group; Manage quality, timeliness, efficiency, and high scientific standards for group; Ensure deliverables comply with B&SR, TA and regulatory guidelines globally; Establish and maintain sound working relationships with partners and customers; Challenge and review (e. g. CDP review, significant protocols and analyses); Ensure high quality Health Authority interactions and external relations; Recruit talent, coach and develop reports on site; As appropriate, take on Program Statistician role for a clinical development program in the TA area; Act as site head for Biostatistics group. Requirements At least PhD in Statistics (or equivalent degree/knowledge/expertise). Fluent English (oral and written). Usually 8 years of relevant Pharma Industry experience Experience as Project Statistician for International Clinical Teams. Strong skills in leading people, operations, and innovation Expert knowledge in clinical trial methodology and in statistics and its application in clinical trials. Excellent knowledge of drug development and commercialisation process and relevant guidelines. Good Project Management skills. Very good communication skills. Background medical knowledge, preferably in relation to the Infectious Diseases therapeutic area.. £0.00 - Contact seller

Contribute to the development of long-term goals and operating policies for the

Fri, 21 Nov 2008 07:18:55 GMT

SR organisation. Contribute to the development of the CIS organisation through his/her global leadership role on the management team. Lead SR strategy for the group. Manage TA portfolios globally. Manage timeliness, quality and preparation of statistical reporting deliverables and ensure that they comply with CIS, TA and regulatory guidelines globally. Establish and maintain working relationship with partners and customers. Manage resources within the assigned group and share resources as needed with other programming groups to ensure optimal SR support across TAs. Initiate and support continuous improvement initiatives within CIS and cross functionally. Ensure that relevant SOPs/NIPs/Working practices are in place and followed. Review the planned contents of tables/listings/figures for SCE/SCS and project level documents to ensure efficient production and usefulness of output. Recruit talent, coach and develop reports. May act as Site Head for SR. Requirements Post-graduate university or college degree in Life Sciences, Statistics, Mathematics, Computer Science, Medical Informatics or equivalent. Fluent English (oral and written). At least 10 years experience in global drug development, including at least 3 years in a senior programming / statistical role within the pharmaceutical industry. Experience with matrix management and global environment. Excellent knowledge of drug development process. Track record in successful project management. Knowledge of Health Authority guidelines. Good knowledge of statistical programming languages. Proven ability to supervise others. Proven ability to lead high impact global cross functional teams. Proven ability to proactively identify issues communicates awareness and recommend/ implement solutions. Strong knowledge and understanding of scientific background of TA, of global and local policies, procedures and practices.. £0.00 - Contact seller

The Sr. Statistical Programmers major activities are as follows: Lead

Fri, 21 Nov 2008 07:18:55 GMT

programming activities for a trial, early phase project, indication or publication activities; lead a complex/large project under supervision of a Program Statistician/Group Head. Maintain efficient interfaces with internal and external customers with support of SR management and the Program Statistician. Develop resource plans as required with support of the Group head. Develop and comply with project/study standards and specifications following internal guidelines; make certain that documents and specifications are consistent and comply with company standards by providing input into study protocol, CRF and data structures tables, listings and figures for phase I-IV clinical trials and submission activities. Program, according to specifications, analysis datasets, pooled datasets, listings, tables, and figures for phase I-IV clinical trials and for SCS and SCE with high quality and within milestones. In conclusion with the statistician, develop specifications for analysis datasets, pooled datasets and listings. Support quality control and quality audit of deliverables 9) Maintain records for all assigned projects and archiving of trial/project analysis and associated documentation. Participate in the selection of CROs and supervise the SR trial activities of the CROs. Provide input on process improvement initiatives and participate in nonclinical project activities. Requirements Minimum of a BA/BS or equivalent experience in mathematics, statistics, computer science or life science or related field(s). Fluent English (oral and written) Intermediate knowledge of/experience with SAS software Working knowledge of database design/structures. Good understanding of global clinical trial practices, procedures, methodologies. Good understanding of regulatory requirements relevant to SR(e. g. GCP,ICH) Intermediate knowledge of office tools. At least 4 years experience in a programming role preferably supporting clinical trials/or in the pharmaceutical industry (2 years for Ms Statistics/Computer Science graduates).. £0.00 - Contact seller

Clinical Contracts Manager - Hertfordshire - Up to 3 days a week field based An

Fri, 21 Nov 2008 07:18:54 GMT

excellent opportunity to work with a top global Pharmaceutical company who are currently developing a number of diverse and exciting products. Working within this large company will be an outstanding opportunity to broaden your experience, enabling you to take your next step up the career ladder. This position is office based in Hertfordshire with the flexibility to work up to 3 days a week from home. Role Summary To lead and manage activities for the outsourcing of clinical services, negotiation and maintenance of contracts for CROs as well as technical suppliers. You will also be responsible for supporting, implementing and managing global outsourcing - including budgets tracking, saving, metrics and audit status and performance of external suppliers. Main Duties and Responsibilities Coordinating Requests for Proposal, CRO presentations, budget analysis, and service provider selection Clarifying scope of work, budget, timelines, roles and responsibilities with internal teams Tracking status of contracts, negotiating change orders / amendments to contracts as required, ensuring terms, conditions, milestones and payments schedules are adhered to. Supporting project teams in the identification and resolution of performance issues Liaising closely with the Legal department, and liaising closely as needed with international affiliates Maintaining knowledge on service provider services and capabilities and industry trends, developing and implementing new processes for outsourcing Qualifications and Experience *First degree a minimum. *Second degree or CIPS qualification desirable. Experience of negotiating and tracking progress of clinical contracts, ensuring compliance with contracts during progress of projects, liaison and consultation with legal department. Knowledge and experience of monitoring CRO performance metrics Experience required: Minimum 3 years relevant experience of managing clinical contracts within the pharmaceutical industry or within the CRO environment to include experience in: negotiation of contracts with CROs, technical service providers, consultants etc. Skills and aptitude required: Must have good written and oral communication skills Team player Able to form strong cross-functional relationships, demonstrating an ability to influence/persuade others Flexible Proactive Good analytical and problem solving skills Eye for detail Highly organised Good leadership skills Strong negotiation skills Key Words: Clinical Contracts Manager Pharmaceutical Hertfordshire Field Based South East North London West London Central London Buckinghamshire Bedfordshire Cambridgeshire Essex Middlesex. £0.00 - Contact seller

A fantastic opportunity to Join a top Pharmaceutical company based in Central

Fri, 21 Nov 2008 07:18:54 GMT

London. With three main areas of therapeutic focus you will have the opportunity to gain specialist working knowledge. The main objective of this role is to provide Clinical Pharmacology strategies and tactical input into study design, methodology and protocol development of Phase I studies with particular emphasis on entry into human, drug - drug interaction, special population bioavailbility and ADME studies. You will ideally have a Phd or equivalent degree and extensive experience in PK/Clin Pharmacology. Additionally they are looking for someone who is interested in developing and implementing a new system, you will also have the ability to work across cultures and you will at times have to exhibit leadership on a project . Responsibilities: *Evaluate and interpret PK/PD data generated during development and provide PK/PD input into Phase I study reports. *Develops and is responsible for scientific expertise on the Clinical Pharmacology and Pharmacodynamics of assigned company pipeline compounds. *Be familiar with all important software (WinNonLin, WinNonMix, NonMem, etc) used in PK/PD analysis and modeling. *Contribute clinical pharmacology expertise to interpretation and understanding of Clinical Pharmacology studies. *Is responsible for the creation of Pharmacology non clinical regulatory documents: Investigational New Drug Applications (INDs), Regulatory Briefing Documents, Investigational Brochures, Investigational Medicinal Product Dossiers (IMPD), Common Technical Documents (CTD) as the basis for New Drug Applications (NDA) in the US and Market Authorization Applications (MAA) in the EU, IND annual reports, EMEA/CHMP documents, and scientific white papers. *Drafts Clinical Pharmacology written interactions with FDA and EU regulatory agencies. *Establish the reputation of the company with Key Opinion Leaders, practitioners, partners and agents, and the public at large. *Collaboratively interacts with scientists from alliance partners. Essentials: Ph. D. or international equivalent degree preferred and 5+ years of PK/Clin Pharm experience in Pharmaceutical R&D, CRO or other relevant experience, or M. S. and 10+ years of PK/Clin Pharm experience in Pharmaceutical R&D, CRO or other relevant experience. Degree is expected in relevant scientific area, e. g. , Pharmacology, Pharmacokinetics, Pharmacodynamics, Drug Metabolism, Pharmacy, etc. Experience in designing PK & implementing PK aspects of clinical trials. Strong knowledge of PK and PK/PD evaluation techniques in interpretation of clinical pharmacology studies. Experience of writing PK sections in clinical study reports. High level of skill in comprehension/synthesis of complex data. Excellent skills in oral and written communication. KEY WORDS: Pharmacokinetics PK Pharmacology Phase I Central London. £0.00 - Contact seller

Exciting field-based CRA (Clinical Research Associate) career opportunities at a

Fri, 21 Nov 2008 07:18:53 GMT

sought-after pharmaceutical company in Dublin! Previous Irish clinical monitoring experience is a must-have. Our client is a leader in its field with over 500 staff in the UK and has a truly global international development programme. They have a very strong pipeline with expertise across several therapeutic areas. They are now recruiting a field-based CRA to join their team based in Ireland. The Role and your Responsibilities The field-based CRA (Clinical Research Associate) will be part of a dynamic team with a big pipeline working on a mix of therapeutic areas, monitoring sites in Ireland and around Dublin. The team provides a lot of support and training to their clinical research staff. They also have an in-house department looking after the ethics, site contracts further supporting their CRAs. This role will require Ireland-wide monitoring with some sites in and around Dublin. The company's offices are based In Dublin. What is Required Previous clinical monitoring experience In Ireland, preferably Previous work experience as a CRA (Clinical Research Associate) Proven clinical experience across several therapeutic areas, Oncology preferred though not essential. Willingness to travel 50-60% of the time Full driving licence Candidates must be eligible to work in Ireland. What is Offered Field-based position Excellent support and training opportunities Dynamic friendly team Permanent contract competitive package & great benefits Immediate start Please send your CV today to find out more about this fantastic career opportunity.. £40,000.00 - Contact seller

Exciting office-based CRA contract opportunity at a sought-after pharmaceutical

Fri, 21 Nov 2008 07:18:53 GMT

company in Dublin! Previous Irish monitoring experience is a must-have. We currently have a contract opportunity for an office-based Clinical Research Associate to monitor in Ireland. This will be a 9-month contract position based in Dublin. The Role and your Responsibilities You will be responsible for the monitoring of studies across different therapeutic areas for studies that are performed in Ireland. You will perform CRA duties from site initiation, site monitoring to site close-out visits. Setting study commitments and ensuring milestones adhered to. Identification of clinical investigators, feasibility assessments and selection visits. Start-up, monitoring and close-out of clinical studies carried out at sites in Ireland. Preparation of Patient/subject informed consent forms for clinical studies. Liaison with others members of study team, locally and globally To ensure studies are monitored according to relevant guidelines, GCP and the companys standard operating procedures. Continuously assess sites performance, processes to ensure site remains on track with recruitment potential. Management of the Trial Master File and Investigator Site files for clinical studies as per GCP Management of the creation and maintenance of study-specific forms Additional duties will be to organise and plan study-related meetings, handle telephone and other enquiries from study site staff and clients during a study, as appropriate and the management of the reporting of adverse events, To update databases for all relevant clinical trial centres and update any study specific tracking systems where required. Willingness to help with monitoring other projects as the need arises What is Required 1 A life-science degree, nursing qualification or equivalent experience 2 The ability to self motivate and work unsupervised 3 Excellent planning and organisational skills 4 The ability to effectively multi-task and be proactive 5 The ability to motivate study-site personnel and study team 6 Excellent communication and negotiation skills 7 Flexibility to travel across Ireland 8 Previous experience as a Clinical Research Associate, with proven track record of monitoring studies to agreed timelines 9 Must be eligible to work in Ireland What is OfferedAn exciting 9-month contract CRA opportunity Office-based in Dublin Contract with DOCS offered with excellent salary & benefits, seconded to our client Immediate start. £40,000.00 - Contact seller

Dublin-based contract opportunity for a Senior Clinical Research Associate

Fri, 21 Nov 2008 07:18:53 GMT

(SCRA)/Project Manager (PM). Sought-after pharmaceutical company in Dublin! Previous Irish clinical monitoring experience is a must-have. We currently have a contract opportunity for an office-based Senior Clinical Research Associate (SCRA)/Project Manager (PM) to part-monitor and part project manage international studies in Ireland. This will be a 9-month contract position based in Dublin. The Role and your Responsibilities You will be responsible for the monitoring and managing of studies across different therapeutic areas. You will perform senior monitoring visits as well as be responsible for studies management and attending Pan-European project management meetings. The successful candidate will have experience within the Irish/UK regulatory environment, in particular contributing to study feasibility, leadership of site selection and set-up and in the management of a study team to deliver to milestones. As a Senior Clinical Research Associate (SCRA)/Project Manager (PM), you will ensure that the conduct of the trial is in compliance with the currently approved protocol/amendment(s), with ICH-GCP, and with applicable regulatory requirement. You can expect to be responsible for site and/or project management of your allocated studies, in accordance with compliance to internal and regulatory requirements. The focus at all times will be your sites and enabling them to deliver on their commitments, hence site monitoring will also be a part of the role. Within the management of your studies you may well be asked to mentor and lead more junior team members, adding significant people management aspects to your profile. Responsibilities: Setting study commitments and ensuring milestones adhered to. Identification of clinical investigators, feasibility assessments and selection visits. Start-up, monitoring and close-out of clinical studies carried out at sites in Ireland. Preparation of Patient/subject informed consent forms for clinical studies. Liaison with others members of study team, locally and globally To ensure studies are monitored according to relevant guidelines, GCP and the companys standard operating procedures. Continuously assess sites performance, processes to ensure site remains on track with recruitment potential. Management of the Trial Master File and Investigator Site files for clinical studies as per GCP Management of the creation and maintenance of study-specific forms Additional duties will be to organise and plan study-related meetings, handle telephone and other enquiries from study site staff and clients during a study, as appropriate and the management of the reporting of adverse events, To update databases for all relevant clinical trial centres and update any study specific tracking systems where required. Willingness to help with monitoring other projects as the need arises What is Required 1 A life-science degree, nursing qualification or equivalent experience 2 Senior monitoring and study management proven experience, ideally in Ireland 3 Previous experience as a Senior Clinical Research Associate (SCRA), with proven track record of monitoring studies to agreed timelines 4 The ability to self motivate and work unsupervised 5 Excellent planning and organisational skills 6 The ability to effectively multi-task and be proactive 7 The ability to motivate study-site personnel and study team 8 Excellent communication and negotiation skills 9 Flexibility to travel across Ireland and Europe 10 Must be eligible to work in Ireland What is Offered An exciting 9-month contract CRA opportunity Office-based in Dublin Permanent contract with DOCS offered with excellent salary & benefits January start Please send your CV today to find out more about this fantastic career opportunity.. £40,000.00 - Contact seller

Our client is a leading solutions-driven CRO committed to therapeutic focus and

Thu, 20 Nov 2008 07:20:46 GMT

operational expertise to deliver clinical trial services of the highest quality for biopharmaceutical and medical device companies. If sounds like the type of company you are looking to be involved with then this may be the job for you. You will identify and qualify business opportunities related to potential projects requiring clinical research services both for target and exploratory accounts. You will assist in proposal development and facilitate any presentations at client sites. To be considered for this role you will be required to have a Bachelors degree in a scientific discipline accompanied by a minimum of three years direct experience in consultative sales. It will be very beneficial if this experience is within a CRO or related service industry. For more details on this outstanding position, a full job description or an informal chat, please call sue Spice at Datatech. £55,000.00 - Contact seller

An exciting and challenging opportunity has become available with a global

Thu, 20 Nov 2008 07:20:46 GMT

clinical research company based in Ely, Cambridge. Our well established client is looking for a Clinical Project Manager who will undertake the design, initiation and monitoring of clinical trials with candidate drugs to the standards of Good Clinical Practice. The Clinical Project Manager will be responsible for the close liaison with clients regarding the management, ongoing status and budget control of projects, under the supervision of the Managing Director. The Project Manager will have direct management responsibilities for junior staff in particular regarding training. To apply for this fantastic position you will have a Biological Sciences degree or nursing qualification, along with significant Project Manager or Senior CRA experience. Furthermore, you will have a keen eye for detail and be able to work in, and motivate a team. This position offers great fringe benefits and an excellent salary. If you would like to hear more please contact Zain Griffiths at DatatechAbout Datatech Search & Selection:- Datatech is part of the highly successful Evergreen Group, where we recognise the value in lasting relationships based on shared opportunity and trust. Our aim is to identify, qualify and deliver talented professionals for our clients, whilst enhancing the careers of those that we place. For more information about us please look at our website.. £0.00 - Contact seller

Our client is a leader in communications and education for healthcare

Thu, 20 Nov 2008 07:20:46 GMT

professionals, with a proud heritage of quality, highest-level service and leadership in regulatory compliance. If this sounds like the type of company you would like to work for then keep reading. You will be responsible for the content development and delivery of medical education and communications projects so that they are delivered in accordance with the project specification, budget and agreed schedule. You will research, write, edit and proof copy to the highest standard for a full range of materials including scientific abstracts papers, posters, oral presentations, print items and multimedia. To be considered for this amazing role you will be educated to degree level or higher in a biomedical science with several years experience in a medical education and communications environment. You will have excellent scientific writing skills and the ability to adapt style and content for different target audiences. For more details on this outstanding position, a full job description or an informal chat, please call Zain Griffiths at Datatech. £0.00 - Contact seller

Our clients aims are to improve both survival rates and the quality of life of

Thu, 20 Nov 2008 07:20:46 GMT

cancer patients by contributing to the evidence-base that will underpin cancer services now and in the future; and to bring about major and continuing improvements in the quality of practice in clinical research. If this sounds like the type of company you want to work for then keep reading! A large amount of your time will be largely spent supporting the QA manager and monitoring team by assisting in the preparation of monitoring visits and keeping track of visits already conducted. You will deal with routine trial queries and pass non-routine and clinical queries to the appropriate staff/professionals. Using your initiative, you will tackle any practical difficulties reported by sites under the guidance of the trial management team and clinical co-ordinator. To be considered for this marvellous opportunity you must have GSCE level Biology or similar subject plus two years experience in a related field. You must also have the ability to travel easily in the UK with overnight stays between visits required on occasions. For more details on this outstanding position, a full job description or an informal chat, please call Natasha Grace at Datatech. £0.00 - Contact seller

Snr Director Investment ContractsOur client is a leading international full

Thu, 20 Nov 2008 07:20:46 GMT

service CRO with locations across the UK and Europe. They are a fantastic company to work for and offer unrivaled opportunity for personal development and career progression. The Role To effectively manage the group activities of Investigator Contracts and Grants Administration (ICGA), including management of ICGA staff and procedures for investigator contracts and budgets, investigator payments administration and investigator grants estimation (Per Subject Costing)Serve as point person for business development (BD) requests (RFIs)/bids/proposals), client presentations or pricing and narratives for each service within 1CGA. Attend BD handoff meetings on behalf of ICGA, post awardPrepare and manage the annual ICGA budget, and subsequently monitor revenue/expenses relative to approved budget as required and assist in revenue recognition. Manage internal and external client relationships with ICGA to meet and manage clients expectation. Maintain open/professional communication with Sponsors, I. C. staff and other employees, as appropriate, in the administration of I. C. services, including issue resolution. EXPERIENCE: Background in science, business/finance or related field. Preferably will have significant experience within a Pharmaceutical/Device/Biotech or CRO5-10 years management experience, with at least one year in a senior management capacity in investigator contracts and grants administration or a related activity. Superior written and oral communication skills. Strong qualitative/quantitative analytical skills. Keywords: senior director, investment contracts, snr investment contracts, director of, investment contracts director, ICGA, biotech, pharma, pharmaceutical, medical devices, cro, contract research organisation, contracts and proposals, licensing, SOP, RFI, finance, clinical trials, clinical research, clinical business, investment, contracts, senior director, business development director,. £0.00 - Contact seller

Regulatory Intelligence Manager EU and InternationalCompany SummaryResearch

Thu, 20 Nov 2008 07:20:46 GMT

based bio pharmaceutical company, rapidly growing to become one of the largest globally, they develop and commercialize medicines in areas of unmet need and have a very strong pipeline and an excellent portfolio of marketed productsJob DescriptionESSENTIAL DUTIES AND RESPONSIBILITIESMonitors primary and secondary sources of regulatory intelligence information e. g. agency websites, databases, journals. Communicates high priority regulatory intelligence information to key customers in real time. Issues bi-weekly regulatory intelligence updates (newsletters) to key customers covering topics under watch, competitor intelligence and other topics as appropriate. Updates and re-prioritizes key topics (topics under watch) and list of competitors relevant to key customers in the business and support related actions as appropriate. Proactively leads, co-ordinates and prepares Companies comments on draft regulatory guidelines through liaising with project teams for provision to Regulatory Authorities with an aim to shaping and influencing the external regulatory environment. Identifies and communicates competitor intelligence associated with regulatory milestones to key customers in the business. Provides responses to ad-hoc requests on regulatory intelligence matters from Regulatory Liaisons and Project Teams. Maintains knowledge of complex regulatory requirements and communicate changes in regulatory information to project teams and senior management in a timely manner. Takes a leadership role in updating and preparing the Company for changes in legislation in assigned territories. Participates in industry trade groups and regulatory affairs professional societies to keep abreast of key issues. Identifies the need for new regulatory SOPs or new revisions to existing regulatory SOPs and prepares the updates/new SOP to ensure compliance with EU legislation. Provides training on SOPs to International Regulatory Affairs Team members. Participates in regulatory team meetings and recognized as a knowledgeable resource of Regulatory Intelligence in other departments. Within the department there lies a strong sense of team work. You will need to be task orientated and be a self-starter and work with minimal supervision. The company will also be looking for you to further develop your external network with professional regulatory associations and industry associations. The International Regulatory Affairs team has a friendly atmosphere and often organizes team-building events and social gatherings, including sports and other social activities. Key Words : MAA Submissions , Regulatory Intelligence , EU NCE , Product Licences, SOP, regulatory intelligence manager, regulatory intelligence management, international, international regulatory affairs team, team leader, project leader, project manager, EU, reg affairs, RA management, RA manager, RA intelligence manager, reg intelligence manager, submissions, QA, CRP, clinical trials, MRP, CTA. £0.00 - Contact seller

Independent Group requires an enthusiastic manager for their newly acquired

Thu, 20 Nov 2008 07:20:46 GMT

branch. Excellent support staff, with support pharmacist. Monday to Friday. 9am - 6pm. Excellent opportunity for experienced Pharmacist/Manager looking for progression. Fully paid management training and minimum paperwork. High salary package for right candidate.. £40,000.00 - Contact seller

Experienced Pharmacy Manager - Urgently required. Must have experience in

Thu, 20 Nov 2008 07:20:46 GMT

dealing with high-volumes. Excellent package available. We are recruiting for one of the largest pharmacy chain providers within the UK with over 1520 pharmacies located primarily in the local community and health centres. The pharmacy delivers a range of diagnostic testing including diabetes screening and Blood Pressure monitoring from its comfortable consultation area. The Pharmacist will have the support of an experienced team including Supervisor and Dispenser. Our clients value their pharmacists and as a large company offer excellent remuneration and benefits with ongoing support and career development at branch level. Benefits include: Competitive Salary 5 weeks Annual Leave Bonus Scheme 2 days paid Study Leave per year for CPD Relocation assistance where applicable Interest Free Loan RPSGB retention fee paid Flexible Benefits Scheme to suit your lifestyle Private Healthcare Company Sick Pay Scheme Company Discount Scheme Contributory Pension & Life Assurance Scheme ... and for Pharmacists coming from EU : Overseas Induction Training for all candidates 4 weeks free accommodation Flight / Travel costs into the UK Continued Local support To find out more information on this exciting opportunity, please get in touch today.... please contact us and send your CV. £43,000.00 - Contact seller

Business Development Executive/PharmaceuticalLicensing, acquisitions and

Thu, 20 Nov 2008 07:20:46 GMT

strategic product development£35,000 + Excellent BenefitsCroydon, Surrey, LondonOur client an established organisation is seeking to recruit a talented Business Development Executive to join their team. The successful candidate will be required to maximise the company's position in the market place. You will be responsible for identifying, evaluating and implementing through to launch for in licensing and product development branded pharmaceutical opportunities. You will have proven experience within a similar role dealing with both licensing and acquisitions within the pharmaceutical industry. ROLES AND ACCOUNTABILITY:1. You will be responsible for identifying profitable opportunities to strengthen and grow the Company's overall business and to expand their global presence. 2. You will be responsible for undertaking market and competition analysis in order to identify and structure new business deals with appropriate partners (e. g. preparation of business cases and scenario modeling in context of the creation of financial and deal models for mid and long term strategy, economic evaluation of the Company's own therapeutic drug projects/products) 3. The post holder will drive in -licensing negotiations, engaging input from all relevant business areas in order to facilitate new business contract 4. The post holder will work from a European perspective as he/she presents the Company in new emerging markets as well as in established markets. The networking responsibility includes the need to interact with business partners on an international level to create collaboration opportunities and to enhance productivity and maintain quality for the Company 5. The professional networking with external partners is a high priority. The post holder will ensure good communication with management and staff to provide expert opinions and recommendations in the market, presenting opportunities and interesting options with clear interpretation and with recommendations for the team 6. The post holder will network with people internally and externally to support the Company's objectives and to create business opportunities 7. A good listener, of patient disposition, tenacious, looking for solutions, places high value on time, and a dependable team player. 8. Ability to work independently and under pressure. KNOWLEDGE AND SKILLS REQUIRED: Demonstrable relationship building and maintenance. Good commercial and marketing and selling skills. Analytical Freedom to travel An understanding of clients needs. A good level of autonomy and good communication skills. Project Management. Negotiating terms/contract Financial Skills Adapting to different cultures. Pharmaceutical Market knowledge Competitor pricing / and tariff. Regulatory know-how Legal framework including trademarks Product and packaging knowledge Multi tasking and organisational skills Presentation skills and personality. Innovation ability to identify opportunities for new products. Decision makers structure and healthcare delivery, financial constraints IT skills particularly with spreadsheetIf you believe you have the key skills and experience for this role, please apply to Evolve Recruitment in Kingston Upon Thames, Surrey.. £35,000.00 - Contact seller

Self motivated and energetic Pharmacists required for Luton and Dunstable areas

Thu, 20 Nov 2008 07:20:45 GMT

. You will be responsible for promoting high standards of retail and dispensary practice, ensuring NHS and OTC growth. A fantastic opportunity offering an attractive salary and benefits package. We are recruiting for one of the largest pharmacy chain providers within the UK with over 1520 pharmacies located primarily in the local community and health centres. The pharmacy delivers a range of diagnostic testing including diabetes screening and Blood Pressure monitoring from its comfortable consultation area. The Pharmacist will have the support of an experienced team including Supervisor and Dispenser. Our clients value their pharmacists and as a large company offer excellent remuneration and benefits with ongoing support and career development at branch level. Benefits include: Competitive Salary 5 weeks Annual Leave Bonus Scheme 2 days paid Study Leave per year for CPD Relocation assistance where applicable Interest Free Loan RPSGB retention fee paid Flexible Benefits Scheme to suit your lifestyle Private Healthcare Company Sick Pay Scheme Company Discount Scheme Contributory Pension & Life Assurance Scheme ... and for Pharmacists coming from EU : Overseas Induction Training for all candidates 4 weeks free accommodation Flight / Travel costs into the UK Continued Local support To find out more information on this exciting opportunity, please get in touch today.... please contact us and send your CV. £45,000.00 - Contact seller

Position: Therapy Area Physician Location: Luton, Bedfordshire The role: We have

Wed, 19 Nov 2008 07:23:36 GMT

an exciting opportunity for a Therapy Area Physician to join us and become a valued expert in the cardiovascular field. As a Therapy Area Physician, you will utilise your knowledge and expertise to maximise the commercial impact of our promotional strategy. This includes having a key role on clinical advisory boards, coordinating medical and regulatory input into brand strategy and delivering clinical plans. The company: If you are looking for an environment that can give you plenty of new challenges, welcome to AstraZeneca. One of the world's leading pharmaceutical companies, we have more than 64,000 people across the globe, an annual turnover in excess of £21 billion - and a wide range of innovative medicines that make a real difference in important areas of clinical need. The successful candidate: The successful candidate will be medically qualified and GMC registered, working in the NHS or in a pharmaceutical company in a similar role, you will be a highly effective communicator with the ability to operate in high calibre cross-functional teams. It is also expected that the successful candidate will have a background in cardiovascular / metabolic disease areas, though for a strong industry medic this is not a pre requisite Keywords Medical Advisor, Medical Affairs, GMC, Therapy Area Physician, Cardiovascular, CNS. £75,000.00 - Contact seller

Position: Therapy Area Physician Location: Luton, Bedfordshire The role: We have

Wed, 19 Nov 2008 07:23:35 GMT

an exciting opportunity for a Therapy Area Physician to join us and become a valued expert in theCNS field. As a Therapy Area Physician, you will utilise your knowledge and expertise to maximise the commercial impact of our promotional strategy. This includes having a key role on clinical advisory boards, coordinating medical and regulatory input into brand strategy and delivering clinical plans. The company: If you are looking for an environment that can give you plenty of new challenges, welcome to AstraZeneca. One of the world's leading pharmaceutical companies, we have more than 64,000 people across the globe, an annual turnover in excess of £21 billion - and a wide range of innovative medicines that make a real difference in important areas of clinical need. The successful candidate: The successful candidate will be medically qualified and GMC registered, working in the NHS or in a pharmaceutical company in a similar role, you will be a highly effective communicator with the ability to operate in high calibre cross-functional teams. It is also expected that the successful candidate will have a background in cardiovascular / metabolic disease areas, though for a strong industry medic this is not a pre requisite Keywords Medical Advisor, Medical Affairs, GMC, Therapy Area Physician, Cardiovascular, CNS. £75,000.00 - Contact seller

A leading Financial Services Organisation is looking to recruit experienced

Wed, 19 Nov 2008 07:23:35 GMT

Pharmaceutical Reps to provide advice to Hospital Doctors and GPs on pensions, protection, savings and investment products. You will undertake face to face customer interviews to recommend and sell suitable products for this Market Leader. This is a home based role, which provides a generous uncapped bonus scheme and excellent benefits package. As a Trainee Adviser you will attend a training programme where you will gain your financial planning qualifications with full support to become a fully competent Financial Adviser. You must have face-to-face Hospital or General Practice sales experience, with a proven record of achieving sales targets. We are looking for candidates who have shown a long-term commitment in previous employment and who are motivated to succeed as a Financial Adviser. As you will be providing advice to High Net Worth individuals you must have excellent communication skills with the confidence to conduct presentations to clients. As this is a home based role you must have a spare room at home which can be converted to an office and hold a full UK driving licence. If you are looking for a change of career then this is a fantastic opportunity to join one of the fastest growing Organisations in the UK. If you want to hear more about this APPLY NOW!. £90,000.00 - Contact seller

A leading Financial Services Organisation is looking to recruit experienced

Wed, 19 Nov 2008 07:23:35 GMT

A Pharmaceutical client of ours is currently looking for a field Sales rep, the

Wed, 19 Nov 2008 07:23:35 GMT

areas you will be covering is based in the South East of England, i. e. ; Kent/ North London/ Surrey/ Sussex etc. You ideally need to have some Sales experience, ideally out on the field, however you NEED to have Pharmaceutical experience or NHS (Experience of the NHS or Pharmaceutical Industry). You could be looking to get out of your current PHARMACEUTICAL job, and looking to get into Sales! Field Sales. This expanding company is looking for the right candidate to join there team, good basic salary + Bonus + Benefits. You need to be confident when meeting clients and you need to be knowledgeable on the Pharmaceutical products that you are selling etc. Duties: Able to establish and build relationships within the professional sectors including retail pharmacists and nurses in Hospitals and Nursing Homes. Skilled in planning and organizing. Smart appearance. Energetic and outgoing person. Proactive, flexible in a rapidly changing environment and committed. Able to take responsibility for decisions and actions. To achieve all sales targets To inform your Area Manager of any trends related to competition, the market or otherwise relevant for the promotion of our products or services. To attend sales meetings, conferences or training programmes, organised by, or for, ......... Pharmaceuticals, where applicable. If this job sounds of interest, then please do call HDS Recruitment Ltd and ask to speak to Danielle for more details.. £0.00 - Contact seller

A Project manager with extensive experience of the CRO or Pharmaceutical market

Wed, 19 Nov 2008 07:23:35 GMT

place is required to fulfill a green field role within this highly specialist consultancy. My client is a rapidly growing organisation with over ten years experience in their field. They are currently inundated with work from a wide range of end clients and the need for a commercially aware individual to provide guidance on best practice, time management and business processes is now vital to their on going growth. As a new role you can expect a high degree of autonomy and responsibility for the entire co-ordination of the Data management element to a number of clinical trials now taking place. As an employer with a low rate of staff attrition you will be joining an established team and the ability to manage their "buy in" to the changes you suggest will be vital to the success of this role. You will work closely with senior Data managers to effect change within the department and liaise with Client project managers to manage expectations and ultimately deliver projects on time, in budget and to my clients usual high standards. The successful candidate will display a career path firmly rooted in the CRO and/or Pharmaceutical arena an obvious understanding of clinical trials and associated data. On a more personal level you will posses excellent communication skills enabling you to engage with all levels of commerce and just as importantly the necessary leadership qualities required to motivate and guide a highly skilled team of professionals. Project managers without an established career in this sector will sadly not be considered for this opportunity. In return for your commitment you can expect a commensurate salary + package and the opportunity to work within a culture that promotes on going training and career advancement. Above all my client has managed to become a highly successful well respected organisation while still retaining the positive aspects of a smaller company.. £0.00 - Contact seller

Job Title
CRA Senior CRA SCRA Clinical Research Associate Senior

Wed, 19 Nov 2008 07:23:35 GMT

Senior Clinical Research Associate

Background (Company)
You'll be joining a company with a presence in more than 30 companies globally and an impressive client portfolio. This is an exciting time in their development with ambitious growth plans in place for 2009. CRAs with more than one years experience can be based from the office or from home in the required countries.

Key Responsibilities
Monitor clinical trials in accordance with ICH-GCP standards
Site management to ensure proper adherence to protocol, source data verification and assess CRF entries
Develop, review and edit clinical trial related
Assist with study protocol design, development and / or review if required

Benefits
Competitive salary
Full benefits package
Excellent career development opportunities - to Lead CRA and Clinical Project Management

Qualifications
Life sciences degree OR nursing qualifications
Minimum of 1 years experience as a CRA
Fluency in local language and familiarity with local regulatory and ethical requirements

To Apply
If you would like to discuss this vacancy further, please call Principal Consultant Stephen McAnaney on 44 (0), or email . If this role is not suitable, Stephen is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

About i-Pharm Consulting
i-Pharm Consulting is a specialist recruitment company focused on mid to high-level roles in Clinical Research & Medical Affairs. We recruit for both permanent and contract staff across the UK & Europe. Our clients include Pharmaceutical, Biotechnology, Contract Research and Medical Device companies. Click on the link for more information:

Key Words
CRA, Senior CRA, SCRA, Senior Clinical Research Associate, Sweden, Sverige, Stockholm, Goteborgs, Gothernburg, Malmo. £0.00 - Contact seller

Senior Pharmacovigilance ScientistOur client is currently looking for an

Tue, 18 Nov 2008 07:21:49 GMT

experience Pharmacovigilance Associate to join their team. This is an excellent opportunity for someone looking to develop their career in a friendly and team focussed environment. The company is working in some very interesting therapy areas and currently has a strong pipeline of products. Duties:Sets work priorities with input from Manager. Acts as a trainer and mentor for more junior pharmacovigilance staff. Receives and reviews adverse event forms for completeness, recognizes discrepancies, enters data into pharmacovigilance database and obtains follow-up information. Identifies methods to improve quality of safety data. Assists in the design and implementation of company SOPs to ensure completeness, correctness and consistency of safety data. Ensures delivery of quality data outputs and periodic reports within defined timelines. Performs document-tracking process for incoming documents, ICSR submission, investigator letter, and CCSI distribution. Works closely with CROs, regarding information exchange and safety exchange agreements. Recognizes potential or impending problems and works with manager to implement solutions. Requirements:3 years of relevant pharmacovigilance experience. BSc Life SciencesKeywords: PV, Pharmacovigilance, Senior, BSc, Drug Safety, Training, South East, senior pharmacovigilance associate, pharmacovigilance officer, reg affairs, pharmacovigilance scientist, SOP, GCP, pharmceutical, pharma, clinical research, clinical trials, clinical studies, clinical study, clinical monitor,. £0.00 - Contact seller

My client based in the south west is looking for a Pharmacist to work within the

Fantastic office-based Senior Clinical Research Associate (SCRA) career

My client based in London is looking for Production Pharmacist to start

Medacs International Plc We are one of the largest suppliers of healthcare

We are looking for a Medical Scientific Liaison manager to work within a

Fantastic home-based/field-based career opportunity for CRAs (Clinical Research

My client based on the south coast is looking for a Pharmacist to start asap for

My client a large hospital based in the North West is looking for a Pharmacist

** SPECIALITY PHARMA COMPANY REQUIRES EXPERIENCED MEDICAL SCIENCE LIASON

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An exciting and challenging opportunity has become available with a global

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Snr Director Investment ContractsOur client is a leading international full

Regulatory Intelligence Manager EU and InternationalCompany SummaryResearch

Independent Group requires an enthusiastic manager for their newly acquired

Experienced Pharmacy Manager - Urgently required. Must have experience in

Business Development Executive/PharmaceuticalLicensing, acquisitions and

Self motivated and energetic Pharmacists required for Luton and Dunstable areas

Position: Therapy Area Physician Location: Luton, Bedfordshire The role: We have

Position: Therapy Area Physician Location: Luton, Bedfordshire The role: We have

A leading Financial Services Organisation is looking to recruit experienced

A leading Financial Services Organisation is looking to recruit experienced

A Pharmaceutical client of ours is currently looking for a field Sales rep, the

A Project manager with extensive experience of the CRO or Pharmaceutical market

Job TitleCRA Senior CRA SCRA Clinical Research Associate Senior

Senior Pharmacovigilance ScientistOur client is currently looking for an

Job Title
CRA Senior CRA SCRA Clinical Research Associate Senior