Clinical Trials Jobs in Berkshire
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Scientific Data Manager
- Salary:
- £40 000 - £50 000
- Location:
- Berkshire
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 15:31Add to My Shortlist
Scientific clinical data manager, Berkshire, permanent role. Wide ranging responsibility including vendor management Introduction Our client is a medium sized, fast growing pharmaceutical company specialising in the proprietary brands and niche generic medicines. This role has opened in response to their increasing need to manage data generated from clinical trials, health economics assessments and market research. In this international role, you will be exposed to data from many clinical indications, and from our client's international subsidiaries. To be considered for this role you must have had previous experience of managing operational budgets as well as being competent in all aspects...
Project Executive
- Salary:
- £18k - £23k pa
- Location:
- Berkshire
- Job Type:
- Permanent
- Date Posted:
- 24-May-2012 10:55Add to My Shortlist
The Role: Within this role you will provide support to operational and account / project team leaders in the development and delivery of project activities, particularly regarding the organisation of meetings, symposia and events for internal and external customers. Our client is an international medical communications agency that develops and produces a broad range of communications programmes and materials on behalf of pharmaceutical industry. Working with pharmaceutical clients, their activities include organising international symposia, developing educational programmes for physicians and patients, producing clinical trial investigator and participant support materials, and developing print/digital materials ranging from sales aids to peer-reviewed publications. The main focus of this project executive role will be to organize and co-ordinate the logistics of meetings and events, ensure planning, administration and tracking of project plans are accurate and internal databases/records are...
Project Executive - Medical Communications - Berkshire
- Salary:
- Excellent Salary Package
- Location:
- Reading
- Job Type:
- Permanent
- Date Posted:
- 29-May-2012 11:01Add to My Shortlist
Project Executives - Medical Communications - Berkshire Quintiles Medical Communications are seeking Project Executives to join their Medical Communications team, situated in Berkshire. Within this role you will provide support to operational and account / project team leaders in the development and delivery of project activities, particularly regarding the organisation of meetings, symposia and events for internal and external customers. The... project/account manager informed of progress. Quintiles Medical Communications is an international medical communications agency that develops and produces a broad range of communications programmes and materials on behalf of pharmaceutical industry. Working with our pharmaceutical clients, our activities include organising international symposia, developing educational programmes for physicians and patients, producing clinical trial investigator and participant support materials, and developing print/digital materials ranging from sales aids to peer-reviewed publications. Successful candidates should have a great eye for detail, strong administration skills and some meetings logistics experience, along with first rate communication skills and ability to see projects through from start to finish. Having...
SAS Programmer - South East England
- Salary:
- Neg
- Location:
- Berkshire
- Job Type:
- Permanent
- Date Posted:
- 30-May-2012 14:43Add to My Shortlist
This is a great chance to work for a truly global organisation with offices in over 40 countries and more than 10,000 employees worldwide We are looking for an experienced SAS programmer to join the team in the UK, you will have the choice of which office you would like to be based in. In this position you will work... statistical appendices with appropriate documentation * Oversee the Quality Review of the statistical reporting of selected projects Qualifications * BSc degree in statistics, computer science or related field is desirable. However also acceptable is a non-graduate qualification in combination with good relevant proven industry and SAS programming experience in a clinical trial environment * Understanding of database structures and working with complex data structures If you have the skills and experience for this opportunity please email your 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, ...
Career CTA/ Clinical Trials Administrator
- Salary:
- On Application
- Location:
- Berkshire, South East England
- Job Type:
- Any
- Date Posted:
- 30-May-2012 13:35Add to My Shortlist
Career CTA/ Clinical Trials Administrator Full-time - office based AB1219 Berkshire Our client, a "Times Top 100 Best Places To Work For" are currently looking for a Career Clinical Trials Administrator to join their clinical research teams. Working as Clinical Trials Administrator you will join the clinical team supporting both the management and monitoring staff. Responsibilities to include; - Initiating, typing and editing of correspondence -...
QA Auditor/ QP, Senior Managers Apply Now
- Salary:
- Car allowance, Pension, Bonus
- Location:
- Bracknell
- Job Type:
- Permanent
- Date Posted:
- 28-May-2012 13:15Add to My Shortlist
Associate Director QA (GMP/GDP) and Senior Manager, QA (GMP) 2 New Headcount Openings within Pharmaceutical R&D, Surrey Quality Assurance, GMP, Qualified Person, Superb Permanent Position, Excellent Conditions Introduction Our client stands at the leading edge of science and technology and has an R&D strategy focused on Urology, Diabetes & Metabolism, Renal Medicine, Cardiovascular Disease and Pain. With a healthy and challenging pipeline and over 30 major ongoing projects in late Phase development, the employees here have unrivalled access to personal growth and recognition Working for this leading Pharmaceutical Company you will be allowed to innovate, accelerate research using your own intuition and enable patient benefit whether it is in clinical trials or managing product lifecycle. Do not hesitate to consider these openings, they offer security, autonomy and significant career opportunity. Company growth has resulted in two new headcount openings both to be situated at the company's European office close to the M25 near Heathrow. CSL is retained to identify suitable candidates...
Clinical Research Assistant, Moscow office Russia
- Salary:
- negotiable
- Location:
- Maidenhead, Berkshire
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
In the complex world of drug development, PharmaNet/i3 is exactly where you need to be. With offices in more than 30 countries around the world, PharmaNet/i3 has the resources to conduct any study; from a large multi-country, multi-language clinical trial today, to a smaller regional study tomorrow. PharmaNet/i3 works for you on trials of any size, anywhere around the world. Clinical Research Assistant I - Office based Moscow, Russia As Clinical Research Assistant you will be responsible for providing full administrative support to our clinical monitoring team. This is an...
Study Start Up Specialist
- Salary:
- negotiable
- Location:
- Maidenhead, Berkshire
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
In the complex world of drug development, PharmaNet/i3 is exactly where you need to be. With offices in more than 30 countries around the world, PharmaNet/i3 has the resources to conduct any study; from a large multi-country, multi-language clinical trial today, to a smaller regional study tomorrow. PharmaNet/i3 works for you on trials of any size, anywhere around the world. Study Start Up Specialist -office based, Maidenhead, UK As Study Start Up Specialist, you will act as the local specialist on regulatory and ethics processes/documentation requirements for the start-up and...
Contracts Analyst
- Salary:
- Negotiable
- Location:
- Winnersh, Uk
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 00:00Add to My Shortlist
POSITION SUMMARY: Researches and negotiates contract activities in relation to sponsor projects; legal or contract management requirements. Serves as communication liaison between Contracts & Functional Services (C&FS) staff and internal and external customers. Provides functional guidance and keeps C&FS team aware of all contract statuses or pending issues. May train less experienced C&FS staff on departmental SOPs and quality output.... appropriately made and documented. 6.9. Ensure appropriate documentation is maintained for all exceptions. 7.10. Communicates and explains legal and budgetary issues to internal and external parties. 8.11. Establish strong working relationships with customer and internal project teams. 9.12. Negotiates and prepares contracts, budgets and related documents for participation in industry-sponsored clinical trials. 10.13. Facilitates the execution of contracts by company executives or General Counsel. 11.14. Assists Contract Managers or other Contracts & Functional Services staff with the active project management of on-going contract issues; and performs follow-up on all outstanding contract issues. 12.15. May train less experienced C&FS staff on departmental SOPs...
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...
Manager Regulatory Affairs - UK
- Salary:
- Negotiable
- Location:
- Maidenhead, Uk
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
Manager Regulatory Affairs - office based Maidenhead, UK PharmaNet/i3 is recognised as a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies, including therapeutically specialised capabilities for Phase I-IV clinical development, bioanalytical services, and staffing from a single clinical professional to an entire functional team. For intelligent solutions needed to accelerate high quality drug development programs of all sizes around the world, PharmaNet/i3 works for you. As Manager Regulatory Affairs you will lead the coordination of our Global Regulatory Projects and gain the international clinical trials experience that you career deserves. The need to co-ordinate and prepare submissions to various international authorities along with the ability to manage internal teams and handle regular contact with clients and agencies means these opportunities would suit experienced regulatory professionals seeking to further develop there regulatory skills to the next...
Director Strategic Partnership
- Salary:
- negotiable
- Location:
- Maidenhead, Berkshire
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
In the complex world of drug development, PharmaNet/i3 is exactly where you need to be. With offices in more than 30 countries around the world, PharmaNet/i3 has the resources to conduct any study; from a large multi-country, multi-language clinical trial today, to a smaller regional study tomorrow. PharmaNet/i3 works for you on trials of any size, anywhere around the world. Director/Senior Director , Strategic Resourcing In this critical role you will be responsible for managing larger cross-functional or multiple single partnerships by assuming full responsibility for all aspects of partnership...
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...
