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Job Details
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Global Clinical Trial Manager - Late Phase (Post-Authorisation)

Business Type: Pharmaceutical Company, Pharmaceutical Services
Job Type: Clinical Operations, Clinical Study- Trials, Project Management
Job Level: Management
Position: Contract
Location: London
Reference: 210119LMCQ1
Closing Date: 24/02/20
Job Details:

Global Clinical Trial Manager - Late Phase (Post-Authorisation) - BioPharma

i-Pharm Consulting are partnering with a global biopharmaceutical company who are looking for a Global Clinical Trial Manager to post-authorisation and investigator led research across a multitude of therapy areas. Willing to wait up to 3 months for the right candidates.


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.


Global Clinical Trial Manager


You will be involved in:

  • Operational management of post-authorisation studies and investigator led studies
  • Feasibility assessment
  • Contract milestone tracking and advice
  • Publication follow up
  • Manages CRO/Vendors on assigned studies acting as principal point of contact
  • Development and maintenance of RFPs
  • Ensuring project team goals are met
  • Preparation of interim and final clinical study reports
  • Work with Clinical Program Managers to manage the European component of global post-authorisation studies


  • Life Science degree or Nursing background
  • Experience managing Phase IV and Non-Interventional studies
  • Experience in the review and oversight of Investigator Lead trials sought after
  • Strong knowledge of post-marketing requirements
  • Knowledge of different types of post-authorisation safety and efficacy studies
  • Good knowledge and understanding of ICH GCP, GVP, FDA and EMEA regulations and guidelines applicable to post-authorization studies.
  • Excellent teamwork, communication, decision-making and organizational skills


West London


12 Month Contract - Freelance


Competitive Daily Rate


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.


CTM / Clinical Trial Manager / Trial Management / Study Manager / Project Manager / Study Management / Biotech / Biotechnology / Biopharma / Biopharmaceutical / Pharmaceutical / CRO / Clinical Research Organisation / Inflammation / Bowel Disease / Rheumatism / Rheumatology / HIV / Infectious Diseases / Phase IV / Late Phase / Post Marketing / Investigator / Non-Interventional / London / West London / Uxbridge / Hayes / Buckinghamshire / Maidenhead / High Wycombe / Marlow / Slough / Reading

Posted: 17/02/2020 | NPJ Ref: 250440
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