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Clinical Study Management Associate - Biotech - 12m Contract

Business Type: Pharmaceutical Company, Biotechnology Company, Drug Development Company, Freelancer, Pharmaceutical Services
Job Type: Clinical Research Associate (CRA), Clinical Operations, Clinical Study- Trials, Senior Clinical Research Associate (SCRA), Project Management
Job Level: Experienced (non manager)
Position: Contract
Location: London
Reference: 040619LMCQ1
Closing Date: 30/08/19
Job Details:

Clinical Study Management Associate - Biotech - 12 Month Contract

i-Pharm Consulting are seeking on behalf of a major Biotech a Clinical Study Management Associate to support the management of outsourced studies across a range of EU countries. This role will see you supporting Liver Disease studies. This contract is perfect for a CRA with recent 6-12 months Study Management Associate level experience looking to step into Project Management.


Leading Biotech with a global presence in over 100 countries. i-Pharm has been a dedicated recruiter for this client for a number of years and have had great feedback on the company''s career progression, culture and job satisfaction from candidates placed in both permanent and contract positions.


Clinical Study Management Associate


You will be involved in:

  • Supporting management of EU outsourced studies
  • Provide administrative support in site selection and coordination of studies
  • Assist Clinical Trial Managers with vendor and CRO management
  • Co-monitor approx. once every 2 months across a number of EU countries
  • Under supervision of the CTM assist in review of ICFs, CRFs, SOPs, monitoring plans and study reports
  • Support training of Clinical Project Assistants and Clinical Trial Management Associates
  • Support the set up and presenting of investigator meetings


  • Life Science degree
  • Ability to travel 20%
  • Experience in liver disease is preferred but not essential
  • Some Assistant Project Management or Trial Management experience is preferred but not essential
  • MUST HAVE independent monitoring CRA background
  • Good knowledge of ICH-GCP Guidelines


Office Based - West London

2 days work from home flexibility


12 Month Contract - Freelance


£350 per day


i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.


If you would like to discuss this vacancy further, please call Lauren McQuade on +44(0)2031890488, or email If this role is not suitable, Lauren is also available to discuss other possible positions or answer any general questions regarding your career and the current market.


Associate Study Manager / CTMA / Clinical Trial Manager / Trial Management / Trial Management Associate / Study Manager / Associate Project Manager / Study Management / Biotech / Biotechnology / Biopharma / Biopharmaceutical / Pharmaceutical / CRO / Clinical Research Organisation / Inflammation / Liver Disease / GI / Infectious Diseases / HIV / Phase IV / Late Phase / London / West London / Uxbridge / Hayes / Buckinghamshire / Maidenhead / High Wycombe / Marlow / Slough / Reading

Posted: 23/08/2019 | NPJ Ref: 240728
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