Clinical Trials Jobs in England
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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. -...
CTA (Clinical Trial Administrator) Cambridge
- Salary:
- 19-21K + Ben
- Location:
- Cambridge
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
CTA (Clinical Trial Administrator) Cambridge Permanent opportunity Do you have solid UK administrative and IT skills? Are you looking for your first step in clinical research? Then this CTA position is for you! The Role and Responsibilities Our client is looking for a hard-working and efficient administrator with excellent IT skills who is looking for their next career step as a CTA...
Senior Clinical Program Manager
- Salary:
- £50k - £62k pa + 14% Bonus + 25/days holiday
- Location:
- Crawley
- Job Type:
- Permanent
- Date Posted:
- 24-May-2012 00:00Add to My Shortlist
We have an exciting opportunity for an office based Senior Clinical Program Manager for our large global pharmaceutical client. SUMMARY Accountable for all aspects of assigned clinical trials (Phase II through lifecycle management) including leading Clinical Trial Team(s). Lead complex trials or programs or manage trials within an alliance partnership. Responsible for development of reports including providing training opportunities and guidance. Responsible for development of realistic clinical operations plans including timelines and budget planning, as well as program level...
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...
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...
Senior Medical Advisor
- Salary:
- £50 - £70,000
- Location:
- Southampton
- Job Type:
- Permanent
- Date Posted:
- 28-May-2012 09:43Add to My Shortlist
Our client is a global, broad-based health care company devoted to the discovery, development, manufacture and marketing of pharmaceuticals and medical products, including nutritionals, devices and diagnostics. They now have a fantastic new opening for someone to join them as a Senior Medical Advisor. Role responsibilities: To provide medical and scientific support for the marketing and sales of relevant therapeutic...
Senior Medical Information Scientist
- Salary:
- £30500 - £38500 pa + competitive benefits package
- Location:
- Cambridge
- Job Type:
- Temporary/Seasonal
- Date Posted:
- 29-May-2012 09:40Add to My Shortlist
Senior Medical Information Scientist I am currently recruiting for a Senior Medical Information Scientist for a 9 month contract for a privately owned pharmaceutical company that specialises in Pain, Respiratory, Rheumatology and Oncology. They currently have products in the market and a strong pipeline for the future. The role is based at their site in Cambridge. You will be responsible... the role of Medical Information ·Provide training, coaching, feedback and support to members of the Medical Information team Qualifications and experience ·Degree in pharmacy, biology or other relevant life science ·Previous experience in Medical Information role essential ·Knowledge of the ABPI Code of Practice essential ·Ability to interpret scientific and clinical trial data ·Excellent verbal and written communication skills essential ·High attention to detail ·Experience in therapy areas of pain, respiratory and/or rheumatology desirable ·Demonstrates ability to train and coach less experienced medical information professionals Application for this role closes on 1st June 2012. For further information on this or other roles...
Senior Clinical Project Manager (Phase I)
- Salary:
- £380 - £400 p/day
- Location:
- Crawley
- Job Type:
- Contract/Interim
- Date Posted:
- 24-May-2012 00:00Add to My Shortlist
We have an exciting opportunity for an office based contract Senior Clinical Project Management role with a Global blue chip pharmaceutical company. Purpose of the role: Planning and implementation of all operational aspects of assigned Translational Medicine studies (e.g. medium to high complexity studies; first in man, patient studies, multi-center studies, mechanistic studies) from synopsis to reporting according to timelines, budget, operational and quality standards. Responsibilities: Writing clinical protocols and related documents in collaboration with the Clinical trial Team (CTT) Lead the clinical trial protocol development process Lead and matrix manage the global multidisciplinary CTT to ensure all trial deliverables are met according to timelines, budget, quality standards and operational procedures Function as a Lead CTL on studies for Full Development and assist in the coordination of TM related...
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...
Regulatory Affairs Consultant
- Salary:
- 25000 - 40000
- Location:
- Cambridgeshire
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
Job Purpose: To provide regulatory consultancy services to internal and external clients, including preparation, review, submission and project management of regulatory applications. Main accountabilities: *Maintain an awareness of, and provide feedback on, client, industry and regulatory developments to input into the strategic development of the department. *Provide up to date regulatory advice to internal and external clients as required. Prepare, ... responsibilities and these include: - to maintain and promote the reputation of the company as an ethical and expert consultancy company- to maintain the confidentiality of patient, client and company information- to maintain good professional relationships with all external parties in contact with the company, including clients, suppliers, consultants and clinical trial investigators- to maintain good working relationships with colleagues and to enable a team spirit within the company- to contribute ideas on matters affecting the running of the company- to maintain an awareness of the business of the company and of all ongoing projects- to be organised in the planning of...
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...
Senior CRA - UK Clinical Trials
- Salary:
- £35k - £45k pa
- Location:
- Camberley, Croydon, Guildford, Kingston Upon Thames, Richmond Upon Thames, Surrey
- Job Type:
- Permanent
- Date Posted:
- 27-May-2012 18:29Add to My Shortlist
An excellent opportunity is available to join a successful European based Clinical Research Organisation CRO. They require a Senior CRA or Principal CRA to start up and Lead their UK clinical trials. As their Senior Clinical Research Associate SCRA you will be setting up the trials and assisting in the site selections. You will ultimately responsible for the conduct and reporting of the trials. You will act as the key contact with the sponsors, investigator and study teams. My client is looking...
Senior Regulatory Officer
- Salary:
- £42k - £43k pa + Full Benefits package
- Location:
- Camberley
- Job Type:
- Permanent
- Date Posted:
- 28-May-2012 16:53Add to My Shortlist
As the global leader in the ophthalmic marketplace, we are proud to meet the eye care needs of millions of people worldwide. For over 60 years, we have developed, produced and marketed the most advanced products available in ophthalmology. Dedicated to the provision of not only the highest quality eye care products, but to also making significant contributions towards the... our senior regulatory experts, you will prepare and submit high quality and timely regulatory applications to the MHRA/IMB, take the lead in co-ordinating activities with regulatory officers and act as a key UK/Ireland contact. The successful candidate will be able to : -Work autonomously in the compilation and submission of Clinical Trial Applications, Marketing Authorisation Applications, Variations, Renewals, Product Information changes and responses to Requests for Further Information, within specified timelines and to agreed quality standards -Pursue maintenance activities for assigned portfolio to ensure ongoing compliance with local and EU regulations and company procedures -Facilitate discussions at senior level with regard to...
Prinicipal Clinical Research Associate
- Salary:
- £40,000 - £45,000
- Location:
- Cambridge
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 16:48Add to My Shortlist
Principal / Senior Clinical Research Associate We have a new vacancy for a Principal/Senior Clinical Research Associate. Experience of GCP monitoring in the UK is essential (a minimum of 2 year's experience) and exposure to Phase I, II and III is desirable. A good overall understanding of drug development and the clinical trial process is essential. The successful candidate will have demonstrated the ability to work as a Lead CRA and will have strong interpersonal skills to ensure client interactions are efficient and positive. Previous responsibility for mentoring and training junior colleagues will also be advantageous. The Principal/Senior Clinical Research Associate will be...
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...
