C Software Engineer - Cambridge - £28-36k
C , GUI, SQL, Windows

Fri, 21 Nov 2008 07:14:31 GMT

ows, Engineer, Developer

This rapidly expanding research and development company in the heart of Cambridge are looking to add a talented C Software Engineer to their small team. You will be working with cutting edge applications on a number of new and exciting projects.

The ideal software engineer will have strong skills in the following areas;
C
GUI
SQL Databases
Windows applications

You will be educated to a degree level (ideally a 2. 1 in computer science or engineering) and ideally will have worked in an incremental development environment.

Your main responsibilities will include; maintain and develop the companies leading software; work closely with a cross disciplinary team to meet customer requirements; work on windows applications and database back-end projects etc.
C , GUI, SQL, Windows, Engineer, Developer. £36,000.00 - Contact seller

Our client, an international company that provides outsourced development

Thu, 20 Nov 2008 07:15:38 GMT

services to the pharmaceutical and medical industries, is looking to recruit a Clinical Project Manager to work in their Buckinghamshire offices. Within this role you will co-ordinate and manage international clinical studies, ensuring timeframes and targets are met and that project expenditure is kept under control. You will be liaising with customers both internally and externally in order to interpret and develop study requirements. The successful candidate will ideally have background in medicine, science or any other relevant discipline and have a proven project management track record with a thorough knowledge ICH GCP and relevant regulations for the conduct of clinical trials. In return our client is offering a competitive salary and benefits package. To find out more information or apply for this position, please submit your cv via this website today.. £48,000.00 - Contact seller

Our client, an international company that provides outsourced development

Thu, 20 Nov 2008 07:15:38 GMT

services to the pharmaceutical and medical industries, is looking to recruit a Project Manager to work in their Buckinghamshire offices. The successful candidate will be responsible for managing projects to ensure integration, co-ordination and consistency of the project. You will also facilitate, co-ordinate and manage all activities related to the planning, executing and monitoring of each project. In addition you will manage budget and resource expenditures for the project, participate in team meetings and prepare agendas and reports. The ideal candidate will have clinical operational experience, have worked within a clinical research organisation and have an appreciation of the drug development process. In order to be a success in this role you will ideally have experience in the administration of Clinical Trials to ICH GCP standard and have comprehensive understanding of project management principles and applications. The successful candidate will be proficient in using Microsoft Office applications and will have good communication and presentation skills. In return our client is offering a competitive salary and benefits package. To apply for this position, or to find out more information, please submit your cv via this website today.. £45,000.00 - Contact seller

Job Profile

A highly sort after

Thu, 20 Nov 2008 07:15:37 GMT

Associate Director position within a market leading International Research Agency within their Financial Services Sector.

Developing your own portfolio of major UK and UK-based corporations, you will be given ''carte blanche'' authority to grow my clients presence within the Financial Services sector.

Within this Associate Director position you must be able to demonstrate exceptional data analysis skills, relationship building and advisory skills with Consulting Heads and Director within Financial Services corporations.

Company Information

My client is a professional research and consulting organisation, pioneering the use of the Internet and information technology to collect high quality, in-depth data for market research and stakeholder consultation; providing companies with a rounded view of their staff, customers, brands and investors as well as assessing opinion amongst the general public and the media.

Experience & Qualifications

?Experience of day-to-day running MR projects (Including client contact survey design and report writing)

?Experience of online market research

?Wide knowledge of UK financial services markets and sectors gained in either a client or agency environment

?Experience working in a marketing research agency.

?Strong depth and breadth of primary research, across methods (Qualitative and Quantitative) and sectors.

Location: Central London

Salary: £50,000 - £60,000

OTE: £80,000 - £100,000

Additional Benefits: Full Benefits package

Apply online!

To understand more about this excellent opportunity in detail, forward you CV to the contact details below.

This is not the only position we are currently working with and therefore please feel free to contact me if you require any further information.

Contact Details

Contact Name: Neil Brand

Position: Senior Recruitment Consultant.

Email:

Direct Dial:

Mobile:

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Recruitment Consultancy of the Year 2007

FPSG (First People Solutions Group) is an award winning recruitment and HR consultancy offering businesses and candidates total solutions for their recruitment requirements.

We specialise across a variety of industries including Accountancy & Finance, Banking & Financial Services, Call & Contact Centre, Information Technology, Office & Business Support, Commercial, Legal, Retail, Insurance, Sales & Marketing, HR, Public Sector and Procurement.

FPSG also incorporate brands First People Care Solutions servicing the Health and Social Care markets and TEC Group, servicing the Technical, Engineering, Construction and Aviation markets.

FPSG is one of the UK's fastest growing companies achieving 48th position in the 2007 Sunday Times Virgin Fast Track 100, and is proud to be IIP and ISO accredited.

FPSG operates as a recruitment agency in providing permanent job-seeking services and as a recruitment business in providing temporary and contract job-seeking services.

* Glasgow (HQ) * London * Edinburgh * Surrey * Manchester * Leeds * Bristol *

FPSG IS AN EQUAL OPPORTUNITIES EMPLOYER *. £60,000.00 - Contact seller

Role:- Senior Clinical Statistician Salary:-Negotiable Location:- Thames Valley

Thu, 20 Nov 2008 07:15:37 GMT

Area, Commutable from Berkshire, Middlesex, Wiltshire, Oxfordshire, Hertfordshire Employment type:- Permanent This company are a highly respected research organisation who are involved with a variety of high profile international trials. They are seeking a Senior Clinical Statistician to add to their current team due to their extensive trial pipeline creating the need for additional support within the statistics team. Having an excellent reputation worldwide this organisation are looking to recruit the highest calibre candidates to integrate into their world class team. The Senior Clinical Statistician will be responsible for the design, monitoring and analysis of specific projects spanning current clinical trials. The Senior Clinical Statistician will also be responsible for the line management of junior members of the statistics team ensuring that they reach their potential. Other major activities within the role will include trial design, generation of randomisation schemes, development of statistics analysis plans and overseeing the programming and validation of analysis databases and statistical tables. The Senior Clinical Statistician will need to possess a degree, MSc or PhD level qualification in a field related to statistics coupled with experience within a clinical setting. It would be beneficial if the Senior Clinical Statistician had expertise in SAS or STATA software packages. Excellent communication skills are going to be paramount to someone being successful in this role as the role involves dealing with people at all levels. Keywords:-Biostatistics Statistics, SAS Data management clinical clinical trial statistician biostatistician Middlesex London Berkshire Buckinghamshire Surrey Hertfordshire Middlesex SAS Oracle Clinical ClinTrials CRO Pharmaceutical Programmer Analyst SAS Analyst Clinical Research Clinical Data Data Management SAS STATA R. £50,000.00 - Contact seller

Role:-Data Management Project Manager Salary:-Negotiable Location:

Wed, 19 Nov 2008 07:18:54 GMT

- Cambridgeshire (Some Flexibility) Employment type: - Permanent A well established CRO are looking to strengthen their Statistics and Data management team with a Data Management Project Manager. With a wide range of high profile clients worldwide this company are getting involved with many cutting edge trials and the Data Management Project Manager will have the opportunity to be working at the forefront of the industry. The Data Management Project Manager will be responsible for allocating and co-ordinating Data Management resources and expertise to individual studies taking responsibility for delivering individual projects on time and on budget. The objectives of each project will vary according to the requirements of the sponsor company and adherence to industry standards such as CDISC will be of paramount importance. . The Data Management Project Manager will need to have had data management experience within either a CRO or Pharmaceutical company. The Data Management Project Manager will need to have taken responsibility for the data management of entire studies or parts of a study having had exposure to the allocation of expertise (data managers, data associates) and budgeting. Familiarity with data management standards such as CDISC would be beneficial. Keywords:-Project Manager, Biostatistics, Statistics, SAS Base, Data management, clinical, clinical trial, statistician, biostatistician, Cheshire, North West, Senior Statistician, SAS Macro, Oracle Clinical, ClinTrials, CRO, Pharmaceutical, Programmer Analyst, SAS Analyst, Clinical Research, Clinical Data, Data Management, SAS.. £0.00 - Contact seller

Role:- Clinical Data Protection Associate Salary:-£18-25k Location:-Hampshire

Tue, 18 Nov 2008 07:17:57 GMT

Employment type: - Permanent This company are one of the fastest growing CROs in the world with a ever increasing presence in the market, with their dynamic attitude and focus on providing innovative and effective solutions for their clients their current path of growth looks set to continue beyond the foreseeable future. The Clinical Data Protection Associate will be responsible for ensuring that the companys data protection code of conduct and associated laws are upheld with the appropriate systems and procedures being put in place. The Clinical Data Protection Associate will in essence be the data protection champion for the site and it will be their responsibility to keep up to date with any changes in the law and to answer any questions other members of staff may have regarding data protection. The Clinical Data Protection Associate will need to have a background in science or medicine, someone who has been a clinical trials administrator (CTA) would be ideal. Knowledge or experience of data protection legislation would be advantageous. Keywords:- Biostatistics, Bioinformatics, Statistician, SAS, StatXact, Nquery, Clinical , Projects, Data Management, South East, Hampshire, Berkshire, Buckinghamshire, Hertfordshire, Middlesex, Hampshire, Surrey. £25,000.00 - Contact seller

Senior Medical Writer

Job Details:

Tue, 18 Nov 2008 07:17:57 GMT
/>·To write, edit and manage the production of high quality clinical documentation (e. g. Clinical Study Reports and Summary Documents) for submission to regulatory authorities in support of marketing applications.
·Act as a member of clinical trial teams following protocol finalisation and to write and edit clinical study reports.
·Participate in the planning of analysis and data presentation to be used in study reports or summary documents.
·Supervise outsourcing to external medical writers.

·Act as program medical writer for various programs in clinical development and ensure medical writing resource allocation to studies within these programs

Our client is a world leader in the Pharmaceutical Industry responsible for creating innovative products focusing on the prevention and cure of disease. Based in Horsham, West Sussex, this large blue chip organisation has an opportunity for a Senior Medical Writer to work within their Pharmaceuticals division.

The ideal candidate will have a Degree in Life Science or equivalent, medical writing experience preferably from within a pharmaceutical organisation. You will have the ability to interpret and present data, have a good understanding of clinical documentation, regulatory requirements and clinical development. With experience in managing external medical writers you will also posses knowledge o document publishing.

In addition to a highly competitive salary the organisation offers an excellent benefits package and good working conditions including free parking, subsidised canteen, social and recreational facilities.

The Scientific Division of Harris Lord was established at client request, we recruit specialists within the pharmaceutical, clinical trials and data management sectors.

Key words: medical writing, clinical documentation, clinical study reports, clinical development. £37,000.00 - Contact seller

Our client is a prominent global clinical research organization serving the

Sat, 15 Nov 2008 09:33:40 GMT

pharmaceutical, biotechnology and medical device industries with services ranging from full clinical trials management services throughout the clinical trials lifecycle right through product registration support. They are currently seeking a Clinical Data Manager to join their offices in Switzerland.

PRINCIPAL RESPONSIBILITIES include:
?Representing Data Management within the clinical team and liaise with clients
?Primarily involved in study setup and conduct for Data Management activities
?Writing Data Management Plan
?Creation and maintenance of Data Handling Manual
?Database testing
?Writing Validation check specifications, review and testing
?Query and discrepancy management
?Data Review and preparation for Medical Review
?SAE reconciliation
?Perform interim and final database QC
?Working to agreed timelines, budget, liasing closely with the project team
?Involved in Biometrics process improvement

QUALIFICATIONS, KNOWLEDGE & EXPERIENCE:
?Life science degree qualification or higher
?Extensive and relevant experience in Clinical Data Management activities within the pharmaceutical/CRO industry with good understanding of GCP/ICH Guidelines
?Experience with Clinical Data Management Systems
?Knowledge of Clintrial 4. 4 and basic programming skills (PL/SQL, SAS) would be an advantage

PERSONAL SKILLS & ATTRIBUTES:
?A proactive good team player with excellent interpersonal, communication skills and detail orientated
?Must be flexible and able to work to timelines and achieve project deadlines
?Fluent in spoken and written English

BENEFITS OF THE ROLE: There are fantastic career opportunities available with this prominent, global CRO in the clinical development process. The company is an equal opportunities employer, offering a challenging and dynamic work environment in a stimulating, multi-cultural atmosphere. Their salaries are competitive and are offered together with an attractive compensation package including a bonus and a range of excellent social benefits including pension, healthcare and company relocation.

Fforde is acting as a recruitment agency/business.

KEY WORDS: Clinical Data Manager, Clinical Data Manager, Data Management, CDM, DM, CRO, Clintrial, GCP, ICH, Life Science, Drug Development, Switzerland. £0.00 - Contact seller

Our client is a leading provider of clinical trial services to the

Fri, 14 Nov 2008 07:13:15 GMT

pharmaceutical industry. A world class company serving the scientific and health care market, a truly global organisation operating in more then a 130 countries with more than 30,000 employees worldwide. As an organised administrator you will be responsible for inputting and maintaining all appropriate quality metrics for their Horsham site. This role will play a key part in working with all areas of the business in ensuring that quality metrics are accurate and up to date at all times. If you are good at problem solving, have had data anlysis experienceand thrive in a team environment, this could be the job for you! This is a trulyfantastic opportunity to join a fast paced but rewarding team! If this is the position for you, then we want to hear from you now!. £24,000.00 - Contact seller

Our client is a leading provider of clinical trial services to the

Thu, 13 Nov 2008 10:03:01 GMT

pharmaceutical industry. A world class company serving the scientific and health care market, a truly global organisation operating in more then a 130 countries with more than 30,000 employees worldwide. As an experienced Project manager you will manage and coordinate all technical and service aspects of a project. This will range from initial discussions with clients, development of the project specifications, documentation aspects of setting up the project and management of all project related activities through project/study completion. Ideally you will have relevant experience of distribution and logistics, preferably within a clinical trials or commercial pharmaceutical background. The post holder needs to have excellent organisational, verbal, written and numerical skills.. £32,000.00 - Contact seller

Clinical Project Data ManagerRole:-Project Data Manager Salary:-Negotiable

Wed, 12 Nov 2008 09:35:58 GMT

Location:-Berkshire Employment type:- Permanent This company are one of the most established companies within the pharmaceuticals sector. Being a global company with a fantastic infrastructure they are able to offer potential employees unrivalled training and development as well as extremely competitive packages. With a strong commitment to maintaining the highest of standards they have managed to maintain their position as one of the worlds leading pharmaceutical companies. The Project Data Manager will be responsible for providing support to various studies throughout the EMEA region, this will involve not only managing data but also analysis of the data. Some of the studies will be run in collaboration with other companies so liaising with various departments and organising vast quantities of data will be a part of the role. The Project Data Manager will need to have had experience with data management and analysis within a pharmaceutical company or CRO. In addition the Project Data Manager is expected to be degree educated with excellent technical ability so that they can provide support to others on technical issues. Keywords:-Biostatistics, Statistics, SAS, Data management, clinical, clinical trial, statistician, biostatistician, Middlesex, London, Berkshire, Buckinghamshire, Surrey, Hertfordshire.. £0.00 - Contact seller

Our client, an international company that provides outsourced development

Wed, 12 Nov 2008 09:35:58 GMT

Our client, an international company that provides outsourced development

Wed, 12 Nov 2008 09:35:58 GMT

Our Client a TOP Pharmaceutical company are now looking to recruit a SCRA with

Wed, 12 Nov 2008 09:35:57 GMT

at least 5 years or an established Junior Project Manager to move into their Clinical Operations Manager Role. It is a fantastic opportunity which is very rare, you will be given support and guidance to progress your career and develop your skills. The position is a permanent role and is office based in the Cambridgeshire area. Responsibilities: Manages the feasibility process Plan, manages and executes all company sponsored study related activities within the affiliate. Ensures the timeliness and quality of study deliverables in accordance with SOPs , ICH GCP guidelines and local regulations. Actively contributes to results oriented department goals Supervising CRO activity, in order to ensure that agreed milestones and enrolment target are met and that high quality data are collected by CRO Ensuring the adequate decisions on Site selections Requirements. *Minimum of 4 years experience in pharmaceutical or Biotechnology or in a CRO *SCRA level or Higher * Good decision making skills *Time management skills BSc or equivalent. KEY WORDS: SCRA JPM Junior Project Management Oncology CRO Pharmaceutical Biotechnology Cambridge Office Based. £0.00 - Contact seller

Our client, an international company that provides outsourced development

Wed, 12 Nov 2008 09:35:57 GMT

Clinical Contracts Manager Company Summary My client has a strong track record

Tue, 11 Nov 2008 07:21:56 GMT

of success in the development, manufacture and commercialization of first-in-class products that significantly improve human healthcare. Specialising in a number of therapeutic areas this is a fantastic opportunity for an individual with prior experience in clinical contract management. Role Summary: A new opportunity within the internal contracts group, but reporting directly to their HQ in Europe. You will be required to manage the investigator / institution clinical trial agreements in relation to a large scale Phase IV observational study, with 150 sites across the world (some of which are already set-up and initiated) . In the long-term this role may also include the set-up of investigator initiation study contracts, and to assist within the UK contracts group. Duties and Responsibilities: Independently plan, initiate, negotiate and execute clinical trial agreements, consultant and other third party contracts: *Effective and proactive contract management to achieve study specifications, timelines, and budgets. *Accurately maintain contracts database. *Initiate, process, track site payments against contractual obligations. *Responsible for development of investigational site budgets based on the study protocol. *Negotiate and execute service agreements for assigned studies. *Evaluate changes in assigned clinical development program/projects to determine the impact on contractual agreements. *Responsible for approving all clinical trial expenditures and ensuring that expense is as agreed by contract. *Clinical trial performance reporting, presentations, other special projects. *Possibility of involvement in set-up of investigator initiated studies Education and Qualifications Required:Bachelors Degree or equivalent experience required. Minimum 1 years experience as a Clinical Contracts Manager / Associate in either CRO, Pharma or Biotech OR Three plus years related experience in both legal and financial negotiations in the pharmaceutical industry As this is an ongoing study the candidate will be able to 'hit the ground running' - so will need strong prior experience of managing investigator site contracts Key Words: Contracts Manager Site Agreements Pharmaceutical Biotechnology Research and Development Berkshire Hampshire Oxfordshire Surrey Middlesex London West London UK Anywhere Relocatable Legal Finance International Phase IV. £0.00 - Contact seller

Clinical Project Assistant Our client is a leading international clinical

Tue, 11 Nov 2008 07:21:56 GMT

research organisation who provides full range of services to the Pharma and Biotechnology industry. As a leading CRO they offer great prospects and career opportunities for their employees along with competitive salaries and benefits. The role Project Assistants (PA) are responsible for providing project administrative support to Clinical Team Managers, Project Managers and/or CRAs on designated project teams. Responsible for all administrative aspects of allocated studies, including maintenance of files and trial tracking databases. Duties and responsibilities - Responsible for the background administration and preparation for trial set up, monitoring, tracking and close out. - Maintaining of project files and documentation in an orderly manner according to the relevant SOPs and WPDs - Assisting in the organisation of investigator, project team and client meetings - May assist in preparation of Regulatory and Ethics Committee packages. Requirements 0-1 year general administration experience. Clinical research administration experience is desirable. Bachelor's or higher graduate degree in a science related field.. £0.00 - Contact seller

Junior Project Manager / Project Manager - Hertfordshire - Fantastic chance for

Tue, 11 Nov 2008 07:21:56 GMT

SCRA to progress to PM Company Summary Are you a Senior CRA looking to take the next step, or are you a junior Project Manager looking to gain international experience at a dynamic and expanding international Pharmaceutical company? My client is currently seeking a Junior Project Manager, or Project Manager, they are based in Hertfordshire and have a broad spectrum of products and specialisms. They have a very exciting pipeline with projects in all stages of development, with unparalleled opportunities for long-term career progression. The company will also offer excellent levels of flexibility - they have an established flexitime scheme, allowing you to beat the rush-hour and you can also be home-based for a number of days a week if you wish! Job Description To coordinate designated parts of the operational aspects of a clinical research study within a European or global clinical development programme . The study leader may also lead, with supervision, the multi functional study team, co-ordinating operational activities and working closely with other team members from other areas of the company. Main Duties and Responsibilities Coordinating designated parts of operational clinical research activities for a study or series of small studies sponsored my client whether directly or through a CRO. Undertaking site assessment and selection and assisting in CRO assessment and selection. Acting as main point of contact for the study sites or for the project managers of CROs Developing a sound understanding of the therapeutic area (CNS) to co-ordinate activities of other more junior members of staff. Co-ordinating the development of site manuals, monitoring manuals and other study documentation and may coordinate protocol drafting, review and finalisation, CRF drafting, review and finalisation and final study report drafting, review and finalisation. Communicating with upper management, negotiating study site agreements, budgets and set and track the study progress and budget using validated clinical trial management tools and systems. Taking responsibility for quality of data for those studies to which he or she is assigned. Undertaking site selection/initiation/monitoring and close-out visits in UK, other European countries and South Africa when required. This will normally be co-visits with CRO staff Responsibility for day to day management of SCRAs, CRAs working on the study and providing input into objectives and appraisals for these personnel. Qualifications and Education : Suitably qualified in relevant Science discipline. Demonstrated clinical research experience to include at least one year as a clinical study coordinator / lead / lead CRA in the EU/ROW country and experience in one other European country and full understanding of current ICH/GCP guidelines. Key Words: Associate Manager Clinical Trial Manager Clinical Study Manager Clinical Project Manager AM SM CTM TM CPM PM Hertfordshire Field Based North London Central London West London Middlesex Buckinghamshire Essex Cambridgeshire Surrey South East Relocatable. £48,000.00 - Contact seller

Principal Clinical Data Manager - Horsham, West Sussex £salary competitive

Sat, 08 Nov 2008 07:19:12 GMT

+ private healthcare + pension Are you an extremely motivated, highly experienced Senior Clinical Data Manager who is looking for an opportunity to grow professionally and have a direct impact on the success of the company This company are looking for a sharp, talented person who works well independently, has the expertise to champion projects, who enjoys interacting with clients and motivating a team It's a great environment and a great opportunity for the right person Principal Duties and Responsibilities As a Principal Clinical Data Manager you will use your extensive knowledge and data management experience to provide oversight and coordination in the day-to-day management of data management projects ensuring that quality deliverables are on time, within budget and according to client expectations; provide input into proposals regarding resources and study deliverables; serve as primary contact with clients to ensure appropriate communication and timely updates. In addition to exceptional project management skills, you will also need strong people management and communication skills to effectively lead your internal team. You will have the ability to motivate and provide guidance to the study team. They will look to you as a leader/resource to provide direction/feedback into study related issues. You will review work produced by project teams and ensure all activities are meeting SOPs and client expectations. Plus you will be responsible for creating performance goals and performing staff appraisals for you team, as well as conducting on-to-one and team meetings. Profile Successful candidates will have a Bachelors degree in life sciences or related discipline or equivalent work experience; at least 5 years of Clinical Data Management experience from within the CRO/Pharmaceutical industry with at least 3 years leading and overseeing a CDM team; and be proficient in a Windows environment. Previous experience with eDC (electronic data capture) is strongly preferred. We offer a competitive benefits package, a pleasant working environment that stresses individual and team achievements, a commitment to work life balance, and outstanding career opportunities.. £50,000.00 - Contact seller

Clinical Data Associate ll - Horsham West Sussex Competitive salary + pension

Sat, 08 Nov 2008 07:19:12 GMT

+ private healthcare This rapidly growing CRO are seeking ambitious individuals to join their growing clinical data management group based in Horsham, West Sussex, to support paper based and electronic data capture clinical trials. We provide excellent training, personal development, career opportunities, international placements and a competitive package of salary, pension, private healthcare and other benefits Responsibilities Provide input into the professional management and coordination of clinical trial data (Phases I to IV). Ensure ongoing data entry from CRFs or other sources into the clinical trial database within agreed time frames to a high standard of accuracy. Identify, resolve or query problematical data observed during data entry raised by electronic checks or manual review. Perform timely update of tracking databases in order to maintain an accurate status of data processing e. g. data entered, cleaned and QC'd. Be able to provide status information on allocated data to the Trial Data Manager. Communicate effectively as appropriate with the client e. g. via e-mail with monitors in order to manage allocated data. Contribute into the design and usability testing of new databases and validation programming. Profile We are seeking Life Science graduates (or equivalenet qualifications) for entrance Data Management positions (CDA II), to join our rapidly growing Clinical Data Management group based in West Sussex. Successful candidates will become part of a fast paced and highly innovative team as a Clinical Data Associate II and as such will be responsible for supporting clinical trial data management at the cutting edge. Ideally degree in life sciences, pharmacy, nursing or nursing qualification (e. g. RN) but equivalent degree level qualifications considered. Good organisational, interpersonal and communication skills and the ability to operate effectively in a team environment. The individual needs to be able to work calmly under pressure and meet deadlines. A dynamic individual with a professional, positive and enthusiastic attitude. The individual should have a basic understanding of medical terminology, clinical trial methodology and ICH/GCP and the drug development process. They should have an investigative and meticulous approach to all activities and tasks and proven ability with clinical databases or equivalent. £30,000.00 - Contact seller

Organisation DescriptionWorking on the statistical development, oversight and

Sat, 08 Nov 2008 07:19:12 GMT

analysis of a number of phase III randomised clinical trials. This includes work on sub-studies associated with the main trials, such as quality of life, health economic evaluation and biological studies aimed at identifying markers of therapeutic sensitivity, which allows the opportunity to work with novel statistical methodology. The post holder will have a remit to work on specific trials whilst the scope exists to widen knowledge and experience as new projects arise. In the first instance the post holder will prioritise work on two studies. The first is a large phase III trial evaluating different types of chemotherapy for breast cancer. This trial (TACT2) is currently open to recruitment with over 100 new patients entered per month. The post holder will also be involved in the exploratory analysis of a large, international phase III breast cancer trial (IES) evaluating the safety and efficacy of a novel endocrine agent. The main clinical results have already been reported but hypothesis generating analyses are being explored. Job DescriptionWorking under the guidance of Senior Statisticians and the ICR-CTSU Scientific Lead for each trial, specific duties and responsibilities will include some or all of the following:Initiation and design of trialsDevelop and define the study question as part of the Protocol Development Group (with clinical colleagues, proposed chief investigator, ICR-CTSU Scientific lead, Senior Trials Manager). This will often include a review of the available literature and analysis of data available to date from other sources. Develop the trial protocol with Protocol Development Group, particularly the statistical considerations of sample size and analysis strategy. Advise on the design of Case Report Forms and trial databases to ensure data are collected and stored to meet the requirements of statistical monitoring and analysis, and in line with relevant guidelines and legislation (e. g. Data Protection Act, EU Clinical Trials Directive, Research Governance Framework, ICH Statistical Principles for Clinical Trials, Good Clinical Practice). Liaise with potential investigators to ascertain likely levels of accrual. With the trial co-ordinator, develop trial literature (trial promotion, patient information leaflets, documentation for competent authority and ethics committee submissions). Contribute as required to funding submissions to external grant awarding bodies and submissions to Research Ethics Committees. Person SpecificationThe role will also involve management and analysis of trials, liaising with trial co-ordinators and data managers to ensure completeness of data during both recruitment and follow up phases of trials. Our client offers fantastic benefits including 30 days holiday per annum.. £36,922.00 - Contact seller

Senior Clinical Data Manager - Horsham, West Sussex £salary competitive

Sat, 08 Nov 2008 07:19:11 GMT

+ pension + private healthcare Are you a highly motivated, experienced Clinical Data Manager who is looking for an opportunity to have a direct impact on the success of the company and have your achievements recognized by Senior Management? This exciting and vital role will enhance your current experience and put you on the path to career advancement. Responsibilities As a Senior Clinical Data Manager you will use your existing knowledge and experience to provide oversight and coordination of clinical data management activities, on both an individual trial and project level. You will be tasked with management of paper based and eDC trials alike. You will monitor the status and progress of data management activities for assigned projects from study start-up to successful database lock to proactively ensure project deliverables meet sponsor requirements, are on schedule and within budget. Additionally, you will perform and often coordinate the following activities: the development and implementation of the Data Management Plan; implementation, coordination, and documentation of database user acceptance testing; data review; query generation; data coding; electronic data reconciliation; identification of protocol deviations; and project status updates to internal management as well as the Sponsor. Additionally, for eDC trials you will be responsible for coordinating site initiation and evaluation along with on site training of personnel on study specific data capture procedures. In addition to strong data and project management skills, you will need strong people management and communication skills to work effectively with your internal team, the client, and, in the case of eDC studies, the site. You will have the ability to motivate and provide mentorship to less experienced members of the Data Management team. They will look to you as a leader/resource to provide guidance/input into study related issues. Your Profile Successful candidates will have a Bachelors degree in life sciences or related discipline or equivalent work experience; at least 4 years of Clinical Data Management experience from within the CRO/Pharmaceutical industry; and be proficient in a Windows environment. Previous experience with eDC (electronic data capture) is strongly preferred. Position also requires superior interpersonal and communication skills; attention to detail; the ability to independently exercise professional judgment; the ability to operate effectively in a deadline driven global environment; and an understanding of resource & budgeting.. £50,000.00 - Contact seller

Role:- Clinical Data Manager Salary:- Negotiable Location:- South East

Sat, 08 Nov 2008 07:19:11 GMT

Employment type: - Permanent One of the largest companies within the Pharmaceuticals and healthcare sector are looking for a Clinical Data Manager to reinforce their existing team, the company require additional support due to the shear volume of innovative trials they have in the pipeline. Being a global company with a fantastic infrastructure they are able to offer Clinical Data Managers unrivalled training and development as well as extremely competitive packages. With a strong commitment to maintaining the highest of standards within their Data Management Function they have managed to maintain their position as one of the worlds leading pharmaceutical companies. . The Clinical Data Manager will be responsible for ensuring that the data acquired throughout the trial is managed according to the sponsor companies requirements. This can involve communicating regularly with the sponsor company, elements of project management, mentoring junior clinical data associates, process improvements and ensuring that all data meets industry guidelines and standards. The Clinical Data Manager will need to be degree educated with at least three years experience in clinical data management. In addition it would be advantageous for a candidate to have experience of EDC (Electronic Data Capture). Keywords:- Clinical Data Manager, CDM, Clinical Data Management, Clinical Report form, CRF, Oracle Clinical, Data, Data Coordinator, Data Manager, Data Management, Programming, Programmer, SAS, Statistician, Pharmaceuticals, Phases I-III Clinical Trials. £0.00 - Contact seller

With the continued growth and expansion within our Client's organisation, we are

Fri, 07 Nov 2008 07:14:21 GMT

looking for a Group Manager to work within the European Clinical Data Management Department. The position will be based in their offices in Scotland. This exciting role will provide the opportunity to be involved in the provision of operational and financial oversight for allocated projects, both Global and European. As Group Manager you may perform a Project Management role for studies with associated services, or act as Franchise Manager for clients. You will provide supervisory functions for Clinical Data Management personnel, including performance management and staff development You will assist Clinical Data Management Senior Management with the formation and implementation of strategic development plans for Clinical Data Management, Europe. To be successful in this role you must be able to apply knowledge and skills in a highly organised fashion, adhering to regulatory guidelines, SOPs and client expectations. You should be able to demonstrate strong customer focus and excellent interpersonal skills. As Group Manager you should be prepared to travel as required and have a flexible and adaptable approach. The successful postholder will have a Life Science Degree or equivalent and extensive experience in Clinical Data Management. Other relevant experience would be considered. Proven supervisory experience is essential.. £0.00 - Contact seller

Role:-Senior Clinical Data Manager Salary:-Negotiable Location:-Scotland

Fri, 07 Nov 2008 07:14:20 GMT

Employment type: - Permanent Currently seeking a Senior Clinical Data Manager this company are one of the fastest growing CROs in the world with a ever increasing presence in the market, with their dynamic attitude and focus on providing innovative and effective solutions for their clients their current path of growth looks set to continue beyond the foreseeable future. The Senior Clinical Data Manager will be integral to the growth of the Clinical Data Management division which is in need of someone with extensive Clinical Data Management experience to support the existing Data Managers working on the varied and exciting trials being conducted at this company. The Senior Clinical Data Manager will be responsible for ensuring that the data acquired throughout the trial is managed according to the sponsor companies requirements. This can involve communicating regularly with the sponsor company, elements of project management, mentoring junior clinical data associates, process improvements and ensuring that all data meets industry guidelines and standards. The Senior Clinical Data Manager will need to be degree educated with at least three years experience in clinical data management. In addition it would be advantageous for a candidate to have experience of EDC (Electronic Data Capture). Keywords:- Clinical data management, CDISC, Clinical Data Associate, Senior data manager, Clintrials, SAS, Pharmaceutical, CRO, Scotland, Glasgow, Edinburgh, Aberdeen.. £0.00 - Contact seller

Senior Clinical Data Manager - Office Based - Permanent Company Summary A

Fri, 07 Nov 2008 07:14:20 GMT

fantastic opportunity to work for a TOP 20 Global Pharmaceutical Company. The company are based in Hertfordshire and have a broad spectrum of products and Specialisms. They are a fantastic company to work for who have firm plans for UK expansion in the next couple of years, creating excellent prospects for career progression. Role Summary The successful candidate will coordinate, lead and perform Data Management activities. This will include CRF design, validation processing, query resolution, DM documentation and liaising with clinical, CRO and statistical departments. Duties and Responsibilities Plan and coordinate database design, development, implementation, maintenance, and user support of clinical systems Program, test, and document databases in accordance with programming standards and validation procedures Provide technical database specifications, data transfer specifications and coordinate transfers of data for internal and external clients Provide technical programming support for data management status and metrics reports Provide technical expertise and guidance for creation and maintenance of CRF and database structure standards Serve as Data Management representative for clinical database related issues, train and mentor junior team members Participate in SOP development process Qualifications and Experience Must be educated to first degree level, Masters Degree desirable but not essential The candidate should have experience within data management in the pharmaceutical or health related industry, managing and co-ordinating projects, and experience in managing contractors and/or data managers. Proven knowledge of GCP and clinical research drug development process Expert knowledge of PL/SQL and logic Knowledge of clinical study protocols and amendments Key Words: Clinical Data Manager Senior Data Manager Pharmaceutical West London London Berkshire Middlesex Surrey Hertfordshire UK Anywhere Relocatable DM CDM PDM Project Data Manager. £0.00 - Contact seller

Role:- Senior Clinical Data Manager Salary:- Negotiable Location:- South East

Wed, 05 Nov 2008 07:20:24 GMT

Employment type: - Permanent This company are one of the fastest growing and most dynamic companies involved in the Clinical research industry. As a specialist contract research organisation they have capitalised on recent market trends as more and more Pharmaceutical companies seek to outsource their research operations to effective and efficient companies such as this CRO. The Senior Clinical Data Manager will be responsible for ensuring that the data acquired throughout the trial is managed according to the sponsor companies requirements. This can involve communicating regularly with the sponsor company, elements of project management, mentoring junior clinical data associates, process improvements and ensuring that all data meets industry guidelines and standards. The Senior Clinical Data Manager will need to be degree educated with at least three years experience in clinical data management. In addition it would be advantageous for a candidate to have experience of EDC (Electronic Data Capture). Keywords:- Clinical Data manager Clinical Data manager, CDM, Clinical Data Management, Clinical Report form, CRF, Oracle Clinical, Data, Data Coordinator, Data Manager, Data Management, Programming, Programmer, SAS, Statistician, Pharmaceuticals, Phases I-III Clinical Trials. £0.00 - Contact seller

As a Data Entry Technician with INC ResearchYou would perform clinical data

Wed, 05 Nov 2008 07:20:24 GMT

entry, verification, and quality control (QC) checks. This would be your first step on the Clinical Data Management career ladder 1. Uses multiple platforms to enter data from case report forms (CRFs) ensuring the fidelity between the CRF and the clinical database of record. 2. Performs accurate and timely data tracking, entry, verification, and QC checks of clinical data into the clinical database as governed by the Data Entry Instruction Manuals, SOPs and communicated policies of the department and sponsor. 3. Makes accurate corrections to the database as requested by the Senior Data Entry Technician, Group Manager, Lead Data Manager or internal auditor in accordance with relevant SOPs/WIs. 4. Identifies any data issues encountered during entry to Data Management in accordance with relevant SOPs/WIs. 5. Handles CRFs and protocol information in a confidential manner. 6. Assists with pre-processing, filing, scanning, indexing, and archivals as assigned. 7. Participates in Data Entry screen development through database testing, and functionality for new protocols 8. Participates in project specific training as required. Perform other work-related duties as assigned. Minimal travel may be required (up to 5%). Requires a high school education or equivalent, data entry experience or equivalent combination of education and experience that provide the skills and knowledge necessary to perform the job. Experience in a regulated environment (SOPs, QA, or Clinical Data) and familiarity with medical terminology preferred. Requires good organizational, planning, and time management skills with a team-oriented approach. Proficiency in Microsoft Office Suite and email is necessary.. £19,000.00 - Contact seller

REF: 39453 EDU: Degree EXP: 1 - 4Years SAL: 30K - 50K LOC: DUBLIN WEST, DUBLIN

Sun, 05 Oct 2008 07:08:34 GMT

NORTH, DUBLIN SOUTH KEY: SENIOR CLINICAL DATA CO-ORDINATOR My client is a provider of services and solutions to the pharmaceutical, medical devices, biopharmaceutical, healthcare and biotechnology industries in the world. With offices in every continent and a staff population of over 18,000, my client is the largest company in its industry in the world. Presently, applications are welcome from candidates with previous experience in clinical data management Serve as Data Operations Coordinator (DOC) for one or two global studies with fewer than 10 operations staff (excludes DE), or serve in a leadership role to a specific DM Task. Manage delivery of projects through full data management study life-cycle (with minimal guidance). With guidance from DTL or Manager, manage project timelines and quality; determine resource needs; identify out-of-scope work. Serve as back-up for Data Operations Coordinator or Data Team Lead (with guidance). Perform comprehensive data management tasks including data review, writing and resolving data clarifications. Perform database designer activities for technologies not requiring extensive programming. Perform comprehensive quality control procedures. Independently bring project solutions to the CDM team. Solve issues through using the global issue escalation/communication plan. Consult with Standards Group for process issues; communicate ideas for process improvement. Assist in developing and implementing new technology. Understand and comply with core operating procedures and working instructions. Meet objectives as assigned. Develop and maintain good communications and working relationships with CDM team. Interact with CDM team members to negotiate timelines and responsibilities. Good understanding of clinical drug development process Background in medical terminology, Pharmacology, Anatomy and Physiology Excellent organizational, communication and data management skills (details oriented) Ability to establish and maintain effective working relationships with coworkers, managers and clients For immediate consideration for this role please apply online or contact: Shane Browne - (01) 632 1865 HRM Science Selection Team YOUR CV WILL BE TREATED WITH THE STRICTEST CONFIDENCE Specialists in [Scientific Jobs] [Pharmaceutical Jobs] [Biotechnology Jobs] [Laboratory Jobs] [Chemistry Jobs] [Quality Jobs] [Clinical Jobs] [Graduate Jobs] [Medical Jobs] [Food Jobs] [Medical Device Jobs] [Pharmacy Jobs] [Clinical Research Jobs] [Nursing Jobs] [Dublin Jobs] [Irish Jobs] [Science Jobs] [Engineering Jobs] [Radiography Jobs] [Regulatory Affairs Jobs] [Analytical Jobs] [Microbiology Jobs] We Always Want to Hear From [Consultants] [Laboratory Technicians] [Lab Analysts] [Health & Safety Officers] [Scientists] [Medical Scientists] [Quality Control Analysts] [Quality Assurance Analysts] [Doctors] [Chemists] [Analytical Chemists] [Pharmacologists] [Biochemists] [Microbiologists] [Quality Managers] [Radiographers] [Quality Engineers] [Qualified Persons] [Pharmacists] and all other scientific and medical professionals... We Can Offer You [Expert Advice] [Interview Tips, Techniques & Strategy] [Salary & Benefits Advice] [Career Counselling] [A Smooth Straightforward Recruitment Process from Start-to-Finish]. £50,000.00 - Contact seller

REF: 39456 EDU: Degree EXP: 3 - 5Years SAL: 40 - 60K LOC: DUBLIN WEST, DUBLIN

Sun, 05 Oct 2008 07:08:34 GMT

NORTH, DUBLIN SOUTH KEY: SENIOR CLINICAL DATA CO-ORDINATOR DEPARTMENT: Data Management JOB TITLE: Data Management Project Leader REPORTS TO: Biometrics Operations Manager/Director or other appropriate manager 1. PURPOSE OF THE JOB: To coordinate and manage the activities of the data management studies and staff in a manner that ensures all timeframes and targets are met to the sponsors satisfaction and that costs are kept under control. 2. RESPONSIBILITIES/AUTHORITIES: Manages and Develops Team Capability Effectively manage and appraise all staff within jurisdiction (or assist in staff management as appropriate). Oversee the day-to-day activities and task management of the project team to ensure a focus on quality, budget and timelines on each project is reached and maintained. Ensure all necessary training is provided to staff to improve their job performance and knowledge. Maintain documentation of training as appropriate. Assist appropriate manager with planning and scheduling. Delivers Project to Quality, Timeline and Budget Requirements Plan, implement and deliver the project in accordance with the contract agreed with the sponsor. Manage projects in a timely manner in adherence with companies SOPs and appropriate regulations, and to liaise with other departmental and project managers as necessary to achieve this. Monitor compliance of the team with SOPs and provide feedback to appropriate manager. Continually review the project contract in order to ensure that any out of scope work is managed promptly and efficiently. Liaise with sponsors on project-related matters. Keep senior management informed of project status in relation to quality and timelines. Influences Critical Decision-making and Thinking Utilise personal experience and knowledge to enhance performance. Effectively direct, motivate, monitor and manage work priorities of self and direct reports. Demonstrate consistent ability to prioritise responsibilities and meet project/department timelines. Identify, discuss and negotiate resolution of issues/concerns with appropriate groups in an open and timely manner. Thorough knowledge of all aspects of Data Management. Good interpersonal skills and the ability to communicate effectively at all levels. Maintains and Develops Processes and Systems Review, assess and implement new technologies as appropriate. Review and assess existing Data Management SOPs. Review new Data Management SOPs. Researches and recommends new data management processes which address customer needs and key business objectives. For immediate consideration for this role please apply online or contact: Shane Browne - (01) 632 1865 HRM Science Selection Team Specialists in [Scientific Jobs] [Pharmaceutical Jobs] [Biotechnology Jobs] [Laboratory Jobs] [Chemistry Jobs] [Quality Jobs] [Clinical Jobs] [Graduate Jobs] [Medical Jobs] [Food Jobs] [Medical Device Jobs] [Pharmacy Jobs] [Clinical Research Jobs] [Nursing Jobs] [Dublin Jobs] [Irish Jobs] [Science Jobs] [Engineering Jobs] [Radiography Jobs] [Regulatory Affairs Jobs] [Analytical Jobs] [Microbiology Jobs] We Always Want to Hear From [Consultants] [Laboratory Technicians] [Lab Analysts] [Health & Safety Officers] [Scientists] [Medical Scientists] [Quality Control Analysts] [Quality Assurance Analysts] [Doctors] [Chemists] [Analytical Chemists] [Pharmacologists] [Biochemists] [Microbiologists] [Quality Managers] [Radiographers] [Quality Engineers] [Qualified Persons] [Pharmacists] and all other scientific and medical professionals... We Can Offer You [Expert Advice] [Interview Tips, Techniques & Strategy] [Salary & Benefits Advice] [Career Counselling] [A Smooth Straightforward Recruitment Process from Start-to-Finish]. £60,000.00 - Contact seller

OVER VIEWMy client is looking for someone to work on a number of challenging

Thu, 14 Aug 2008 07:14:56 GMT

Phase I / II / III clinical trials. Your responsibilities will include, but are not limited to: * Performing discrepancy management and generation/resolution of DCFs * Performing manual checking and pre-entry review of CRFs * SAE reconciliation * Medical coding within Oracle Clinical * Basic tasks in building Oracle Clinical/SAS/Excel databases to pre-approved database specifications * Data entry when required You will have previous relevant data management experience with experience in Oracle Clinical considered as essential. If you think you have what it takes, please apply, attaching your CV and advising of your availability and salary expectations. TECHNICAL - Performing discrepancy management and generation/resolution of DCFs - Performing manual checking and pre-entry review of CRFs - SAE reconciliation - Medical coding within Oracle Clinical - Basic tasks in building Oracle Clinical/SAS/Excel databases to pre-approved database specifications - Data entry when required ADMINISTRATION - Production of database build supporting documentation such as annotated CRFs - Preparation of study documentation, e. g. Data Management Plan, manual checks documentation, Data Entry guidelines etc. - Tracking of CRFs and DCFs - Maintenance of Data Management PDFs and H drive GENERAL - Providing accurate Data Management metrics to the Study Data Managers when required and updates to management via email and at meetings - Attendance at meetings within Data Management, across the company or with external vendors/CROs e. g. study team meetings - Input into Data Management specific SOPs AS APPLICABLE - Basic CRF Design tasks including maintaining CRF library pages, chairing CRF Review meetings and liasing with external CRF Printing companies. Working closely with and taking the lead from the CRF Designer - Back-up Study Data Manager responsibility for ongoing single centre and multi-centre UK and worldwide PI – PIII trials PRIOR EXPERIENCE & PERSONAL TRAITS: Essential Experience, Qualifications, Attributes: - Previous Data Management experience - Data Management experience in basic Oracle Clinical procedures - Good computer skills including knowledge of a range of computer packages e. g. , Microsoft Word, Excel, PowerPoint, Project, email - High level of attention to detail and accuracy - Ability to work within a project team - Highly self-motivated and proactive - Good communication skills both written and verbal - Good planning, time management and organisational skills. £0.00 - Contact seller

My client is a large blue chip pharmaceutical company and they require a

Thu, 14 Aug 2008 07:14:56 GMT

Clinical Data Manager for six months to be based at their Harlow site. Description:* Operational Data Manager role using Inform. * Primary responsibilities may include study management, processing data, managing data flow and all activities from data entry to data clean up and may include Inform database set up. * Prior experience of managing data in Inform is preffered. * An eye for detail, ability to work to timelines and quality standards critical. * The role will require expert organisational skills and sound data management experience in handling data inconsistencies and activities through to locking a database. * As many tasks will be iterative, the role will require patience and ability to retain high standards when working to tight timelines. * There will be interactions with clinical, statisticians and other data management staff. * Good communication skills will be required. * Raising, issuing and resolution of data queries. * Maintenance of data management database documentation. * Cleaning data to GCP If you have previous CDM experience and have ideally used InForm, please apply, attaching your CV and advising of your salary requirements.. £0.00 - Contact seller

My client is a large blue chip pharma company and they require someone for the

Wed, 14 May 2008 06:04:53 GMT

following role:- Experienced data manager. - Project management role within a therapy area using the InForm tool. - Responsible for representing data management within the study team environment. - Responsible for completion of all relevant data management activities during both set-up and maintenance phases of an InForm study. In order to be able to meet their requirments, you will need the following competencies:- Excellent project management skills. - Effective communication skills. - Experience of working in EDC systems, ideally InForm. - Experience of working in multi disciplinary teams. - Sound knowledge of data management processes. - Sound knowledge of the clinical development process - Experience of managing external/non-CRF data from external vendors. - Flexibility, a positive and pro-active attitude and excellent team player skills are all essential. If you feel you have these skills and this experience, please apply, attachign your CV and advising of your salary expectations.. £22.00 - Contact seller

Are you looking for a contract position?Do you have previous Clinical Data

Thu, 13 Mar 2008 06:03:27 GMT

Management experience?ROLE; - Experienced data manager. - Project management role within a therapy area using the InForm tool. - Responsible for representing data management within the study team environment. - Responsible for completion of all relevant data management activities during both set-up and maintenance phases of an InForm study. COMPETENCIES; - Excellent project management skills. - Effective communication skills. - Experience of working in EDC systems, ideally InForm. - Experience of working in multi disciplinary teams. - Sound knowledge of data management processes. - Sound knowledge of the clinical development process - Experience of managing external/non-CRF data from external vendors. - Flexibility, a positive and pro-active attitude and excellent team player skills are all essential. If you are who my client is looking for, please apply, attaching your CV and advising of your availability and salary requirements.. £43,000.00 - Contact seller

C Software Engineer - Cambridge - £28-36kC , GUI, SQL, Windows

Our client, an international company that provides outsourced development

Our client, an international company that provides outsourced development

Job Profile A highly sort after

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Our client, an international company that provides outsourced development

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Organisation DescriptionWorking on the statistical development, oversight and

Senior Clinical Data Manager - Horsham, West Sussex £salary competitive

Role:- Clinical Data Manager Salary:- Negotiable Location:- South East

With the continued growth and expansion within our Client's organisation, we are

Role:-Senior Clinical Data Manager Salary:-Negotiable Location:-Scotland

Senior Clinical Data Manager - Office Based - Permanent Company Summary A

Role:- Senior Clinical Data Manager Salary:- Negotiable Location:- South East

As a Data Entry Technician with INC ResearchYou would perform clinical data

REF: 39453 EDU: Degree EXP: 1 - 4Years SAL: 30K - 50K LOC: DUBLIN WEST, DUBLIN

REF: 39456 EDU: Degree EXP: 3 - 5Years SAL: 40 - 60K LOC: DUBLIN WEST, DUBLIN

OVER VIEWMy client is looking for someone to work on a number of challenging

My client is a large blue chip pharmaceutical company and they require a

My client is a large blue chip pharma company and they require someone for the

Are you looking for a contract position?Do you have previous Clinical Data

C Software Engineer - Cambridge - £28-36k
C , GUI, SQL, Windows

Job Profile

A highly sort after