Clinical Trials Jobs in Cambridgeshire
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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 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...
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...
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...
Principle / Senior Consultant
- Salary:
- 40000 - 60000
- Location:
- Cambridgeshire
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
I'm currently seeking an Experienced Senior Regulatory Affairs Consultant to join medium yet well-established consultancy in Cambridge. This is not a standard Regulatory Affairs Consultant role! My client is seeking a consultant with a good background (at least 5 years) in the development of pharmaceutical and biotechnology products and is already working in Regulatory affairs. Having a consultancy background in Regulatory Affairs would be an advantage. Within your skills repertoire you'll have experience with advanced therapies (gene therapy, somatic cell therapies, tissue engineered products). You'll be able to review development plans against EU / FDA guidelines and advise on regulatory requirements for Clinical Trial & Marketing Applications. If you feel you could be an excellent match then I would love to hear from you Even if you are unsure on your suitability for this position but you are looking at the possibility of some progression in your current job or a change in your...
Senior/ Safety Specialist
- Salary:
- TBC
- Location:
- Cambridge
- Job Type:
- Permanent
- Date Posted:
- 24-May-2012 00:00Add to My Shortlist
Working within the drug safety team, you will be responsible for the overall co-ordination of the serious adverse event (SAE) processes as well as the co-ordination of database activities for projects. You will maintain knowledge and understanding of PPD SOPs and WPDs; current global regulations and ICH/local guidelines regarding clinical trials, regulatory documents and safety issues; and effectively interface with project teams, Client Company, and investigators regarding SAE activities. The Safety Specialist is involved in the preparation and revision of department SOPs and WPDs as well as preparing for and attending audits. Previous PVG/drug safety experience is essential within a pharmaceutical, ...
Clinical Research Associate - Principal/ SCRA Jobs in Cambridgeshire
- Salary:
- £35,000-45,000 pa
- Location:
- Cambridgeshire, Cambridge, Wisbech, Ely, March, Whittlesey, Chatteris, Linton
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 11:58Add to My Shortlist
Clinical Research Associate - Principal/CRA Job in Cambridgeshire Competitive Salary and Benefits Package Flame Pharma are currently working very closely with a growing CRO in Cambridgeshire to recruit an experienced Senior CRA or Principal CRA to join their team in a thriving and active working environment. The Role This position will be varied and Office Based. Reporting to the Head... documentation and participation in client and internal project team meetings amongst other general study-related activities. The Person In order to be considered, the successful candidate must possess proven experience as a CRA in the UK in a Pharmaceutical/Healthcare product development environment. A good overall understanding of the drug development and clinical trial process is essential. Desirable qualifications are BSc / PhD (or equivalent) in a scientific discipline. Candidates will also need the candidate to have competent IT skills include the use of MS Office Applications, Word, Excel, Powerpoint and Outlook. Candidates must have a full clean driving licence and be free to...
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...
GCP QA Auditor
- Salary:
- To Negotiate
- Location:
- England, Hertfordshire, Essex, Cambridgeshire, Bedfordshire
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 16:48Add to My Shortlist
As primarily a GCP QA Auditor within the multi-disciplined company QA team you will utilise your expert regulatory knowledge and excellent communication skills to assist with the design and implementation of the audit programme for the clinical development functions, including internal systems, external supplier and essential documentation and investigator site audits. You will also provide support, advice, education and training to other departments involved in clinical trials and pharmacovigilance activities and may become involved with PV, GLP and GMP audits. You will take part in hosting GCP and PV regulatory inspections; assist with the set up and maintenance of procedures within Clinical Development and support the development, maintenance and audit of marketing authorisation application dossiers. This will...
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...
UK- Experienced Senior Clinical Research Associate
- Salary:
- Competitive
- Location:
- Cambridgeshire, Huntingdonshire, Bedfordshire, Hertfordshire, Northamptonshire, Norfolk
- Job Type:
- Permanent
- Date Posted:
- 29-May-2012 00:00Add to My Shortlist
An interesting and varied Lead/Senior Clinical Research Associate vacancy has arisen with our client; a progressive Clinical Research Organisation and regulatory consultancy which specialises in providing practical advice and support to the pharmaceutical industry to move products from early concept and into the clinic. Their main area of focus is in early Phase clinical trials. The Senior CRA will be responsible for monitoring clinical trials sites and will also be the main point of contact for Investigational site staff. They will also be required to act as Lead CRA on multi centre studies and to mentor new and less experienced members of the CRA team. To...
Experienced Clinical Project Manager
- Salary:
- On application
- Location:
- Cambridgeshire, Huntingdonshire, Bedfordshire, Hertfordshire, Northamptonshire, Norfolk
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 00:00Add to My Shortlist
Experienced Clinical Project Manager (Cambridgeshire, UK) An interesting and varied Clinical Project Manager vacancy has arisen with our client, an expanding Clinical Research Organisation and regulatory consultancy which specialises in providing practical advice and support to the pharmaceutical industry to move products from early concept and into the clinic. Their main area of focus is in early Phase I and Phase II clinical trials. The Project Manager will have primary responsibility for the delivery of Clinical Projects and will be the main point of liaison within the company for the client and associated third-party vendors. The Project Manager will also work with the team to develop and promote the business. This is a permanent, ...
Clinical Research - Senior SAS Programmer Jobs in the Hampshire Area
- Salary:
- £30,000-45,000 pa
- Location:
- Cambridgeshire, Cambridge, Wisbech, Ely, March, Whittlesey, Chatteris, Linton
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 09:58Add to My Shortlist
Clinical Research Job - Senior SAS Programmer Job in the Hampshire Area Salary - Highly Attractive Salary + Excellent Benefits Package Flame Pharma are working with a leading global contract research organization providing discovery and development services and drug lifecycle management. With an enviable client base across pharmaceutical, biotechnology, medical device, academic and government organizations, this organisation are able to... as needed - Ensure projects are well documented and consistent with company SOPs and working procedures The Person - 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 You must be based in the UK to be considered for this position. We can progress applications for experienced Programmers with a background in Pharma, Biotech and Clinical Research if this experience was not gained in the UK....
Senior Manager Regulatory Affairs
- Salary:
- On Application
- Location:
- Cambridgeshire, Bedfordshire, Hertfordshire, London, Middlesex
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
JOB SUMMARY: Exciting opportunity for an experienced regulatory specialist to join a global organisation offering excellent career progression. You will contributing to clinical development plans, global regulatory strategic plans and providing advice on EU regulatory clinical trial and marketing authorisation requirements to the International Project Teams or Regulatory Sub-team. You will also be responsible for maximising product lifecycle management and licence maintenance for our clients current marketed products BACKGROUND: Our client is one of the world's leading research-based pharmaceutical companies with operations in the U.S., Asia, Europe...
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...