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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.


THE COMPANY

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.

TITLE:

Global Clinical Trial Manager

THE ROLE:

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

EXPERIENCE:

  • 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

LOCATION:

West London

DURATION:

12 Month Contract - Freelance

RATE:

Competitive Daily Rate

ABOUT i-PHARM CONSULTING:

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.

www.i-pharmconsulting.com

TO APPLY:

If you would like to discuss this vacancy further, please call Lauren McQuade on +44(0)2031890488, or email lmcquade@i-pharmconsulting.com. 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.

KEYWORDS:

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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