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Clinical Study Manager 12 month contract

Hertfordshire   •  Contract/Temporary, Full time

Clinical Study Manager - Hertfordshire - 12 month contract

Our client is a Specialist Biopharmaceutical company, they are looking to hire a freelance Clinical Study Manager for a position based in


This position focuses on the study development (from concept through to completion), protocol development, CRF design, clinical data review and CSR development.
The ideal Clinical PM/SM will have and MSc or PhD and 2 or more years` experience within a study management role focused on oncology.
This is an excellent position for an experience Clinical Study Manager with a scientific background to work within a progressive pharma, this position offers some home flexibility in a 12 month contact.
Contract length:
12 months
Clinical Study Manager / Clinical PM
Job role:
Within this role the successful CSM / CPM will be implementing and managing Phase I-III oncology trials.

Experience required:
- Experience gained within a Pharmaceutical or Biotech company
- Scientific background
- Degree level education
- 3 or more years` experience managing clinical studies (Clinical Study Manager level)
- Experience of study design, CRF & protocol preparation
- Excellent communication, presentation and influencing skills
- Oncology study experience

Please apply today or contact Josh Craven within the Clinical Team. 01189 594 990 / josh@clinicalprofessionals.co.uk

Job reference:

Clinical Professionals is a leading pharmaceutical staffing business. We have been placing professional within clinical research for over 10 years so have unrivalled 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.

PM, clinical PM, Study Manager, Trial Manager, Clinical Scientist, Research Scientist, clinical studies, pharmaceutical, IND, Phd, GCP, CTD, MMS, NDA, CRF, TMF, Herts, North London, Bucks, Beds, Cambridgeshire, Cambs, clinical operations, pharmd, icf, iec, irb, submissions

You must be eligible to work in the UK. Learn more

  • Agency: Clinical Professionals
  • Posted: 11th August 2017
  • Expires: 22nd September 2017
  • Reference: J30132
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