Clinical Trials Jobs in Buckinghamshire
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Regulatory Affairs Clinical Trial Coordinator
- Salary:
- £25 - £35 p hour
- Location:
- Buckinghamshire
- Job Type:
- Contract/Interim
- Date Posted:
- 24-May-2012 00:00Add to My Shortlist
A leading, global Pharmaceutical Company are looking to bring on board a Regulatory Affairs Clinical Trial Application Specialist, for a 6 month contract, to their site in Buckinghamshire. Role: - Responsible for managing regulatory aspects for assigned clinical trials (across Phase 1 - Phase 4 and spanning five therapy areas). - Responsible for making sure the required regulatory intelligence is in place. - Lead cross-functional teams. -...
Senior Clinical Research Associate - Buckinghamshire
- Salary:
- £38K + car all and ben
- Location:
- Buckinghamshire
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
Senior Clinical Research Associate - Buckinghamshire This is a fantastic opportunity to join a global organisation renowned for their specialism in respiratory related therapies. The Role and your Responsibilities Objective: Manage sites to ensure patient safety, data integrity and successful, timely completion of clinical trials. Duties: Include identifying and managing trial sites, conducting site visits in all phases and stages of clinical trials, involvement in CRF development and review, assist in negotiation of site budgets, active involvement in developing and refining Clinical Department processes. Start Up Phase: You will be involved in identifying investigators, perform site...
Statistical Programmer - Bucks
- Salary:
- Circa £45k
- Location:
- Buckinghamshire
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
Permanent Headcount Our client is an established leader in the field of Dermatology and attracts and retains well-educated, motivated and results-oriented people who are eager to make a contribution to the development of the company. They are currently looking for a Statistical Programmer. Job Puropse To positively contribute towards increasing the company's financial results and the appropriate use of our client's products by providing programming expertise for clinical trials and support of the computing environment within Clinical Biometrics. Accountabilities Technical Support: Provision of a statistical programming service to our clients Clinical Development in terms of the study set-up and reporting of clinical trials, and support of the Clinical Biometrics computing environment. Quality: Ensure the high quality of information provided by...
Senior Statistical Programmer - Bucks
- Salary:
- Circa £45k
- Location:
- Buckinghamshire
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
Permanent Headcount Our client is an established leader in the field of Dermatology and attracts and retains well-educated, motivated and results-oriented people who are eager to make a contribution to the development of the company. They are currently looking for a Statistical Programmer. Job Puropse To positively contribute towards increasing the company's financial results and the appropriate use of our client's products by providing programming expertise for clinical trials and support of the computing environment within Clinical Biometrics. Accountabilities 1. Technical Support: Provision of a statistical programming service to our clients Clinical Development in terms of the study set-up and reporting of clinical trials, and input to and support of the Clinical Biometrics computing environment. 2. Quality: Ensure the high...
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...
Pharmacovigilance Physician
- Salary:
- Good Salary
- Location:
- Buckinghamshire
- Job Type:
- Permanent
- Date Posted:
- 23-May-2012 18:02Add to My Shortlist
One of our preferred clients has informed us there is an exciting new opportunity for a Pharmacovigilance Physician within Global Medical Safety Job Description: - To work within a global team of physicians with responsiblity for post marketing and clinical trial safety - To provide support and medical leadership to the Pharmacovigilance Operations team. - Primary responsibility for the medical evaluation...
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...
Senior Clinical Data Manager
- Salary:
- Competitive
- Location:
- Maidenhead, High Wycombe, Berkshire, Spain, Madrid, Wooburn Green, Buckinghamshire
- Job Type:
- Permanent
- Date Posted:
- 24-May-2012 00:00Add to My Shortlist
PharmaNet/i3, the inVentiv Health clinical segment, is recognized as a leading provider of global product development services to pharmaceutical, biotechnology, generic drug, and medical device companies, offering therapeutically specialized capabilities for Phase I-IV clinical development, bioanalytical services, and staffing from a single clinical professional to an entire functional team. For a rewarding career in a dynamic environment, PharmaNet/i3 works for...
Medical Assessor - Product Safety, Europe
- Salary:
- On Application
- Location:
- Cambridgeshire, Buckinghamshire, Essex, Hertfordshire, London
- Job Type:
- Permanent
- Date Posted:
- 24-May-2012 09:15Add to My Shortlist
Benefits: Corporate Package JOB SUMMARY Excellent opportunity for a UK GMC registered physician looking to join a leading global pharmaceutical company. Based within the EU HQ you will contribute to the provision of a fist class Pharmacovigilance service by undertaking comprehensive medical evaluation of individual case safety reports (both spontaneous and clinical trial) and supporting the General Safety Officers (GSO) in aggregate report production. BACKGROUND Our client is one of the world's leading research-based pharmaceutical companies. Based in Hertfordshire they employee over 11,000 people worldwide. PRIMARY DUTIES * To provide comprehensive medical evaluation of individual adverse event case safety reports (both spontaneous and...
Senior EU Study Manager (Oncology)
- Salary:
- On Application
- Location:
- Berkshire, Buckinghamshire, Hertfordshire, Surrey, London, Middlesex
- Job Type:
- Permanent
- Date Posted:
- 24-May-2012 09:16Add to My Shortlist
JOB SUMMARY: Senior Study Management of Phase II and Phase III Oncology studies according to ICH guidelines in support of the clinical strategies defined in the Integrated Development Plan (IDP) as they relate to European specific responsibilities. Support of Phase I trials may also be required. Office based from London HQ. BACKGROUND: Expanding Global Pharmaceutical Company EU HQ based in... conducting clinical studies, which includes writing basic study protocols; managing study conduct, including oversight of CROs/other vendors; identifying and resolving study site issues; managing the study budget; and study closeout. QUALIFICATIONS / EXPERIENCE REQUIRED: * Bachelors Degree preferably in Life Sciences, or R.N., or international equivalent. * 3+ years of clinical trial management, Study Manager / Project Manager, experience including accumulation of one year of monitoring experience required (either in a pharmaceutical company or clinical research organization). * 1+ year of European clinical trial management * Demonstrated ability to manage clinical trials * Superior communication skills: written, oral, interpersonal and presentation * Excellent problem...
Senior CRA
- Salary:
- Competitive
- Location:
- Berkshire, Buckinghamshire, London, Leicestershire, Lancashire, Merseyside
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
Benefits: Base Salary / Car / Car Allowance JOB SUMMARY To join this respected Global CRO as a Senior Clinical Research Associate (SCRA). You'll manage site responsibility for clinical studies and mentor junior CRAs. The role is supporting the Oncology team and will be concentrated with trials in the Midlands and the North. The role can based from the Client's Greater London offices or field based either in the Midlands or the North (Manchester area). BACKGROUND A very respected Global CRO with an impressive Client Base and strong portfolio of current clinical studies. PRIMARY DUTIES Management of Clinical Trials Assist in preparation of protocols CRF Design Negotiate Investigator Budgets Recruitment of Investigators Study Site Management Mentoring Junior CRAs Initiation Visits / Monitoring Train Clinical Teams Assist with Business Development QUALIFICATIONS / EXPERIENCE REQUIRED: Graduate in a Science Discipline. Fluent English, verbal and written. A second European language (Italian, Dutch...
Pharmacovigilance and Medical Review Manager
- Salary:
- On Application
- Location:
- Berkshire, Buckinghamshire, Surrey, London
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 09:02Add to My Shortlist
JOB SUMMARY We are seeking to appoint a Pharmacovigilance and Medical Review Manager who will report directly to the Director of their local R&D structure. Covering the UK, the Pharmacovigilance and Medical Review Manager will assist in all aspects of local Medicinal Safety, in accordance with applicable regulatory requirements, guidelines, laws, and Servier quality standards and practices and in close... a leading French independent research based organisation specialising in ethical pharmaceuticals. Servier UK's head office is located in Wexham Springs, Buckinghamshire, at the heart of the UK pharmaceutical industry's cluster in the Thames Valley. PRIMARY DUTIES Ensure all safety reports are managed in compliance with ICH and GCP guidelines for clinical trials and marketed products * Communicates information relating to medicinal safety to Global PV in France, and other internal departments, for clinical trials and marketed products. * Assist in safety management activities with external partners * Actively participates in the maintenance of PV Quality management system> * Coordinates Medical Review for our...
Contract File Reviewer, Stevenage- UK
- Salary:
- On Application
- Location:
- Stevenage, Hertfordshire, Buckinghamshire, Bedfordshire, Cambridgeshire, Essex, Suffolk
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 00:00Add to My Shortlist
Novella Clinical is a global, full service CRO with our European Headquarters in Hertfordshire, England. We are committed to providing a superior service to our global clients, and as such we are seeking to hire the best Clinical Research Professionals in the industry. We are currently looking for an experienced Document Control Specialist to work in our offices based in... are also proud of being one of the very few global CROs to work to the high standards of ISO accreditation. Principal responsibilities will include: * Responsible for coordinating with other departments to ensure all electronic and paper storage needs are prepared and maintained * Maintain contact with project managers, clinical trial managers and CRAs to obtain the necessary documentation throughout the trial, for document quality control * Collaborate in the development, maintenance, and archive of study-related web portals * Collaborate in the development, maintenance, and archive of Novella's electronic document management system, as well as, ensure accuracy and consistency * Assist...
Clinical Research Physician - Oncology, UK
- Salary:
- Excellent + Benefits
- Location:
- Berkshire, Buckinghamshire, Oxfordshire, Hampshire, London, Surrey, Uk
- Job Type:
- Any
- Date Posted:
- 29-May-2012 00:00Add to My Shortlist
Clinical Research Physician - Oncology My client, a leading pharmaceutical organisation with an international presence are looking to recruit a pharmaceutical physician with a background in Oncology at either Associate Director or Director level. Role Detail: Working in a Uk-based role, but as part of a global team, you will be responsible for the management and development of PI -... This is a permanent, office-based role with some international travel when required. To Apply: Please call Toby Ferguson at Only Medics on +44 (0) 1189 522799 or e-mail your CV to toby@onlymedics.com. All applications will be held in absolute confidence. Keywords: medic physician doctor research physician medical affairs clinical development clinical trials pharmacovigilance drug safety GMC Phase I Phase II Phase III Oncology Haematology Hematology Onco-Haematology Haemato-Oncology Cancer Berkshire Buckinghamshire Bedfordshire Hampshire Hertfordshire Middlesex London Surrey UK anywhere re-locate
Study Start Up- UK
- Salary:
- On application
- Location:
- Stevenage, Hertfordshire, Buckinghamshire, Bedfordshire, Cambridgeshire, Essex, Suffolk
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 00:00Add to My Shortlist
Novella Clinical is a global, full service CRO with our European Headquarters in Hertfordshire, England. We are committed to providing a superior service to our global clients, and as such we are seeking to hire the best Study Start Up professionals in the industry. We are currently looking for an experienced Study Start Up Lead to work in offices based... Strong written and verbal communication skills to express complex ideas to study personnel, internal and sponsor team members. * Excellent organizational and interpersonal skills. * Positive attitude and ability to interact with all levels of staff to coordinate and execute study activities. * Ability to manage multiple priorities within various clinical trials. * Working knowledge of current ICH GCP guidelines and applicable regulations. * Ability to reason independently, assess and recommend specific solutions in clinical settings, and mentor entry level start up staff. If you are interested in Novella Clinical and would like to be a part of our team, please submit...