Clinical Study Administrator
- Contract Type
Clinical Study Administrator // Clinical trial Assistant
Cambridge- Homeworking flex
Commutable from Cambridgeshire, Bedfordshire, Essex, Bedford
12 month contract - URGENT
Competitive Daily rate dependent on experience
We have just taken on a Clinical Study Administrator position, with a globally renown Pharmaceutical company based in Cambridge. Our client is look for an experienced Clinical Trials Assistant to aid the Study managers across several clinical studies.
This is an excellent opportunity for a experienced Clinical Study administrator/ Clinical trial assistant, to gain further career exposure and development within a pioneering global Pharma with a large and varied pipeline.
This is a 12 month contract role, based in Cambridge with the potential of homeworking flexibility for the right candidate.
-Support and maintenance of TMF
-Management of Study documentation
-Support the study managers
-Cross trial working
-Coordination of study tasks
The candidate -
-Must have a university degree
-Knowledge of ICH-GCP principles
-Fluent in spoken and written English
-Must have a Life Science or Nursing degree or other healthcare professional equivalent
-Prior experience of clinical trials as a Clinical Trial Administrator or Clinical Trial Coordinator
If you think you have the required skills and would like to apply for this role, please send an updated CV to email@example.com or call for Lisa on 01189594990
Clinical Professionals is a leading pharmaceutical staffing business. We have been placing professional within clinical research for over 10 years so have unrivaled knowledge of the market and can give tailored advice for you and outstanding levels of service throughout your career. We also have great relationships with our clients so pride ourselves on being able to identify clients that may be the perfect fit for you and bring you to their attention. By working proactively with candidates, we find you the RIGHT job at the RIGHT time.