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Job Details
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Clinical Project Associate - Pharma - London (Part Time)

Business Type: Pharmaceutical Company, Biotechnology Company, Drug Development Company, Freelancer, Pharmaceutical Services
Job Type: Clinical Research, Clinical Operations, Clinical Study- Trials, Clinical Administrator - CTA, Feasibility Management
Job Level: Experienced (non manager)
Position: Part Time
Salary: Up to GBP220 per day
Location: London
Reference: 030720LMCQ1
Closing Date: 10/07/20
Job Details:

Clinical Project Associate (Part Time) - Small Pharma - Central London

i-Pharm Consulting are partnering exclusively with a Small Pharmaceutical Company in Central London who are seeking a Clinical Project Associate to join their Clinical Operations team. This pharmaceutical company develops novel treatments within the area of Women''s Health.


  • Reporting directly to the Director of Clinical/Medical
  • Provide support in the management of CROs and other Vendors
  • Assist the Project/Regulatory Lead in the creation of study related materials
  • Tracking of invoices and study payments
  • Management of TMF including generation of documents and TMF review
  • Assist in the preparation of meeting agendas, minutes taking and action item tracking
  • Support all aspects of study progress from planning to close out
  • Support all regulatory requirements (EC submissions)
  • Contract, budget, and invoice management
  • Co-monitoring alongside Regulatory Lead (international)


  • Central London - Office Based
  • (Home based during COVID as per government regulations)


  • Competitive daily rate


  • 6 month rolling contract
  • 3 days per week initially with the opportunity to increase to full time after initial assignment (negotiable)


  • Bachelor''s degree or higher (Scientific or healthcare discipline preferred)
  • Work experience:
    • 2-3+ years'' experience in drug development in the pharmaceutical industry
    • OR
    • 1+ year in industry coupled with NHS or Academia experience
  • Experience working in a clinical operations / clinical project management
  • Ideally exposure to international/global clinical trials
  • Exposure to site activation/SSU activities
  • Knowledge of ICH GCP
  • Proficiency in Microsoft Word, Excel and PowerPoint
  • Must be a self-starter with the ability to multi-task and adapt to a start-up feel company environment

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)20 3189 0488, 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.


Clinical Trial Administrator / CTA / Clinical Trial Assistant / Clinical Trial Associate / Clinical Trials / CPA / Clinical Project Assistant / Clinical Project Associate / Junior Project Manager / Pharmaceutical / Biotech / Biotechnology / Women''s Health / Urology / CRO / Central London / Soho / Mayfair / Marylebone

Posted: 03/07/2020 | NPJ Ref: 255838
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