Clinical Trials Jobs in London
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Senior Contract Analyst, Leading CRO
- Salary:
- Excellent Package and Benefits
- Location:
- West London
- Job Type:
- Permanent
- Date Posted:
- 23-May-2012 14:03Add to My Shortlist
Senior Contracts Analyst Leading CRO based in Berkshire Introduction My client is a leading CRO. With offices around the globe, and across six continents, their UK office is located in Berkshire, and is within easy reach via major transport links. The goal of our client is simple - to assist their customers to develop products for patients more quickly and... CRO Employment Type: Permanent Hours: Full time Location: UK; Office Based - various locations Plan Start Date: 2nd July 2012, Please do not apply if you are unable to meet this start date. Employer Benefits: Company Pension, Life Insurance, Private Healthcare Keywords: MS Office, Site Contracts, Negotiation, CRO, Pharma, Contracts, Clinical Trial Agreements, C&O. Bids, Proposals, Negotiation, Accruals, Financial Assigned Consultant: Kirsty Clark at CSL Recruitment on 01932 234681 Please feel free to call for a detailed Job Description or additional information Applications are reviewed within 24hrs; applicants will only receive feedback if they demonstrate the skills the role requires in their...
Clinical Data Manager
- Salary:
- Circa £25,000 - £30,000 pa
- Location:
- Islington, London
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
Clinical Data Manager Circa £25,000 - £30,000 pa Islington, London 35 hours per week About the Job Here at Cancer Research UK, we're looking to recruit a Clinical Data Manager to join our Drug Development Office (DDO). The DDO identifies promising novel anti-cancer agents in co-operation with UK academic centres and commercial partners around the world. We formulate and manufacture drugs and take them through pre-clinical and phase I and II clinical development. As a Clinical Data Manager, you'll aid in the development of new cancer therapies by managing, processing and producing clinical trials data to a high scientific standard in accordance with regulatory requirements. You'll also lead the data management for your own studies, ensuring the study is in-stream and is managed efficiently and effectively. In addition, you'll maintain the data validation plan for your studies to ensure high quality and consistent data...
Associate, Clinical Trial Supplies
- Salary:
- On Application
- Location:
- Hertfordshire, London, Middlesex, Buckinghamshire
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
JOB SUMMARY: To coordinate, under supervisory direction, IMP packaging, labeling, distribution and accountability activities contributing to the on-time delivery of quality-driven clinical supplies. To collaborate with clinical supply team colleagues and external vendors in the creation of value within the overall clinical development process. PRIMARY DUTIES: Main duties/responsibilities: * Coordinate, under supervisory direction, IMP packaging and labeling activities * Work... study team * Strong organizational and analytical skills, developing ability to work semi-autonomously * Good basic vendor management skills * Strong verbal/written communication and interpersonal skills, especially in the area of relationship management * Proficiency in software applications (Word, Excel, Powerpoint and database management) * Ability to travel (10%) KEYWORDS: Clinical trials supplies, IMP packaging, labeling, distribution TO APPLY: For a confidential discussion please telephone Omar de Bary at AXESS Limited on 020 8560 2300. To apply, please send your CV to jobs@axess.co.uk quoting reference 5184 . Only candidates with EU work authorisation will be considered. ABOUT AXESS: AXESS has been operating...
Statistician - UK (Choice of locations)
- Salary:
- Neg
- Location:
- City Of London
- Job Type:
- Permanent
- Date Posted:
- 30-May-2012 15:06Add to My Shortlist
Superb opportunity to join a truly global organisation in this exciting permanent role We are looking to recruit a statistician to join the Biostatistics and Programming team office based in a choice of locations across the UK Role Responsibilities * Support the lead statistician or lead programmer on projects * Provide statistical support for data summaries and analyses * Suggest... C.V. to Phil@stelfoxuk.com for further details and confidential correspondence Phil is a Clinical Operations and Biometrics Search expert at Stelfox Pharmaceutical Search covering Europe, UK, North America and Asia For more updates on great jobs and opportunities follow Phil on twitter - @Stelfoxclinical Biostatistics , biometrics, Statistics, SAS Data management, clinical, clinical trial, statistician, biostatistician, CRO, Pharmaceutical, Programmer, Analyst, SAS Analyst , Clinical Research, Clinical Data, Data Management, SAS, Statistical programmer, Senior SAS Programmer
Research Nurse
- Salary:
- £30,634 - £40,406 p.a. inc. HCAS.
- Location:
- London, Nw1 2bu
- Job Type:
- Contract/Temp
- Date Posted:
- 25-May-2012 00:00Add to My Shortlist
University College London Hospitals NHS Foundation Trust Are you an oncology nurse looking for a new challenge? An exciting opportunity has arisen. We are expanding the Early Phase Cancer Clinical Trial team and are looking to employ cancer research nurses to support a number of early phase cancer clinical trials within UCLH and the new Wellcome Trust Clinical Research Facility. The post holder will be responsible for the co-ordination and management of the early phase clinical trials associated with multiple tumour types. The...
EU Regulatory Affairs Manager
- Salary:
- Competitive Salary
- Location:
- Buckinghamshire, London
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
My client has a new role through company expansion for Regulatory Affairs Manager EU, The European Regulatory Development team is responsible for all the regulatory activities leading up to positive opinion for new marketing authorisations (global projects) and new clinical indications within the European Union. The team is responsible for strategic input to Global Project Teams via Global Regulatory Affairs and includes regional advice ranging from the regulatory aspects of R&D study design, regulatory intelligence, to the most advantageous filing pathway. Operationally the group co-ordinates the compilation of all clinical trial application documents and oversees CROs who submit these locally, therefore it is essential that you will have previously worked with and managed external vendors. The group will also prepare and submit: EU Scientific Advice; Pediatric Investigation Plans (PIPs); Orphan drug applications; IMPDs in addition to marketing authorisation applications (MAAs) across...
Manager Clinical Operations and Compliance, SOCS CFU
- Salary:
- On Application
- Location:
- Hertfordshire, London
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
BENEFITS: Flexibility to work from home, pension, bonus JOB SUMMARY: Our client is a top tier pharmaceutical organisation based in Hertfordshire. This is a unique role which will combine your knowledge of Clinical Operations, Drug Safety and implementing and managing process. You have strong leadership capabilities with the ability to provide direction for these processes through direct line management of... efforts or inefficient processes. The manager will escalate and identify processes/issues and inform or request appropriate intervention by the Associate Director, Clinical Operations in a proactive manner. The Manager will also collaborate with IT to address any technical/database related issues. * Measure of success would include a positive impact on clinical trial timelines and/or controlled document, training, TMF or SUSAR issues. In addition, establishing innovative methods to streamline or combine activities which facilitate the quality of study trial documentation QUALIFICATIONS / EXPERIENCE REQUIRED: A bachelors in Science or health related discipline. KEYWORDS: Study Trial Administrator, CRA, SCRA, Senior CRA, Drug Safety, Clinical...
Clinical Trial Manager
- Salary:
- £65k - £75k DOE + benefits
- Location:
- London, Kent, Uk
- Job Type:
- Permanent
- Date Posted:
- 23-May-2012 11:42Add to My Shortlist
Our client, an innovative and rapidly expanding Clinical Research Organisation are looking for experienced Clinical Trial Managers to come and join their busy team in South-East London. Your role will be to manage project, timeline and budget deliverables, provide project support and performance management to project team members, supervise CRAs and CTAs on a matrix basis and serve as primary contact...
Training Manager
- Salary:
- £55k - £60k pa
- Location:
- London
- Job Type:
- Permanent
- Date Posted:
- 23-May-2012 17:00Add to My Shortlist
Barclay Meade HR are working on behalf of a leading clinical research organisation who have a requirement for a Training Manager. This is a new and exciting opportunity for a candidate with a strong clinical and training background. Our client are a leading clinical research organisation. The Training Manager will be responsible for the development, organisation and delivery of initial and on-going technical and professional skills programs. The successful candidate will have training development and delivery experience preferably in health care or clinical research. You will also have significant experience in ICH GCP. The role will involve working closely with business partners, in particular Operational Heads to determine the training needs and develop programs for both project specific and internal business requirements. The Training Manager will liaise with various departments...
Training Manager
- Salary:
- £55k - £60k pa
- Location:
- London
- Job Type:
- Permanent
- Date Posted:
- 24-May-2012 14:45Add to My Shortlist
Barclay Meade HR are working on behalf of a leading clinical research organisation who have a requirement for a Training Manager. This is a new and exciting opportunity for a candidate with a strong clinical and training background. Our client are a leading clinical research organisation. The Training Manager will be responsible for the development, organisation and delivery of initial and on-going technical and professional skills programs. The successful candidate will have training development and delivery experience preferably in health care or clinical research. You will also have significant experience in ICH GCP. The role will involve working closely with business partners, in particular Operational Heads to determine the training needs and develop programs for both project specific and internal business requirements. The Training Manager will liaise with various departments...
Training Manager
- Salary:
- £30 p hour
- Location:
- London
- Job Type:
- Contract/Interim
- Date Posted:
- 24-May-2012 09:17Add to My Shortlist
Barclay Meade HR are working on behalf of a leading clinical research organisation who have a requirement for a Training Manager. This is a new and exciting opportunity for a candidate with a strong clinical and training background. Our client are a leading clinical research organisation. The Training Manager will be responsible for the development, organisation and delivery of initial and on-going technical and professional skills programs. The successful candidate will have training development and delivery experience preferably in health care or clinical research. You will also have significant experience in ICH GCP. The role will involve working closely with business partners, in particular Operational Heads to determine the training needs and develop programs for both project specific and internal business requirements. The Training Manager will liaise with various departments...
Biometrics Team Leader - Part time (3 DPW)
- Salary:
- £35-40k (DOE)
- Location:
- London, Uk
- Job Type:
- Permanent
- Date Posted:
- 30-May-2012 00:00Add to My Shortlist
Our client, a charitable foundation committed to conducting clinical research for patient benefit is looking for a Biometrics Team Leader to work with them in their busy London office. With a close affiliation to a local Trust, the charity is involved in Phase I-IV research trials including pharmacokinetic studies in patients, and healthy volunteer studies. The organisation conducts research sponsored by the pharmaceutical industry, non commercial organisations such as the MRC as well as research that it sponsors itself. The Team Leader is responsible for ensuring that all the Company's data management and statistical activities are conducted in accordance with the clinical trials legislation and guidelines. The Biometrics Team leader will manage, co-ordinate, oversee and deliver all data management and statistical activities and provide leadership and management of personnel associated with these activities. The successful candidate will be partly responsible for defining the scope and process for this position, based on their knowledge...
Drug Safety Associate Contract
- Salary:
- On Application
- Location:
- Berkshire, London
- Job Type:
- Contract/Interim
- Date Posted:
- 30-May-2012 10:01Add to My Shortlist
JOB SUMMARY: 3 month contract. We are looking for a technically savvy Pharmacovigilance Scientist or Drug Safety Officer, who is looking to take on more responsibility in a global role. You will have case processing experience and be looking to develop further triage, review and global experience. Your technical expertise and interest in Electronic Reporting (user testing etc), will be... Management Plan, SAE reconciliation plan. * Ensures that all pharmacovigilance reporting requirements are met. QUALIFICATIONS / EXPERIENCE REQUIRED: * Life sciences or nursing degree * Knowledge of pharmacovigilance reporting procedures/requirements within the pharmaceutical industry, with a minimum of 2 years experience. * Experience in processing events from post-marketing sources and clinical trials. * Previous use of safety databases; knowledge of Oracle AERS preferable. * Experience of establishing electronic reporting of ICSRs to European Competent Authorities is highly desirable. * Excellent verbal and written communication skills is essential. * All applicants MUST have a valid UK/EU passport. Tier 1 Visa's unable to be...
Clinical Research Associate/ CRA/ SCRA
- Salary:
- On Application
- Location:
- South East England, London
- Job Type:
- Any
- Date Posted:
- 30-May-2012 13:29Add to My Shortlist
Clinical Research Associate/CRA/SCRA AB-1164 Offered via i3 - full i3 contract + i3 Benefits Field-Based across the South East with good access to central London office Start date: ASAP We currently have a great opportunity for a CRA, you will join an established and friendly team who have a great office location looking out across London. In this role you... years experience (covering SIVs, routine monitoring and closeout) preferably with oncology/ haematology experience. However our client has a wide portfolio and work across a wide range of therapeutic areas. We are seeking an experienced CRA to assume full site management responsibility. You will provide support to investigators conducting commercially sponsored clinical trials and ensure they are working to the highest quality standards and to monitor and report on the progress of trials across the partner institutions where one or more of the partners is acting as sponsor or co-sponsor. You will ensure that investigators and their teams run trials according to sponsor's...
Associate Director Clinical Operations Neuroscience
- Salary:
- On Application
- Location:
- Cambridgeshire, Essex, Hertfordshire, London, Middlesex
- Job Type:
- Permanent
- Date Posted:
- 24-May-2012 09:14Add to My Shortlist
JOB SUMMARY: Rare opportunity for a Senior Project Manager/Programme Manager looking to progress into an Associate Director role within a top tier Pharma Company. This role will involve both strategic and scientific leadership for assigned studies and/or have overall Clinical Operations responsibility for a specified compound within the Neuroscience portfolio. May also have responsibility for direct reports, including hiring and... study-related risks are appropriately identified and managed, and ensuring timely and appropriate escalation of study risks to functional head, Clinical sub-team, Project Review meetings and other appropriate forums. Monitoring resource needs for the assigned studies and works with functional management to ensure that these needs are met. * Management of clinical trial costs within the approved budget for the assigned studies * Achievement of relevant Key Performance Indicators for the assigned studies * Contributing innovative thinking and bringing an external market perspective to task execution within and outside area of direct accountability * Acting as an informal mentor and coach to team...