Science, Pharmaceutical & Food

Clinical Trials Specialist

  • Contract
  • London City, London, UK
  • 41986145

PE Global is currently recruiting for a Clinical Trials Specialist for a 23-month contract with a biopharma client based in London (Hybrid role).


  • BOARD Quarterly MVR GSO Compliance and other metrics
  • SRDO Program Roster updates and maintenance
  • GSO Department Website maintenance
    • Knowledge Manager; responsible for maintaining the department website, GSO Dept Teams locations, and reconciling/filing between Teams and the GSO SharePoint Content Center
  • The below tasks may also be included when unsupported by study staff and/or CRO:
  • eTMF and SharePoint/Teams documents; may include upload, correction, review, and reporting
  • Clerical assistance to arrange internal/external meetings and teleconferences
  • Process documents for DocuSign signatures (e.g., facilitate and/or support IP package review/signatures, ICF signatures)
  • Assist with tracking and review of Clinical Trial Insurance requirements, expiry dates, insurance renewal, certificate distribution, and archival
  • Support mass communications via email or mailings


  • Clinical trial experience either as a study coordinator at a site or CRA OR CTA work within a CRO.
  • Relevant administrative experience including detail oriented, collaborative, positive attitude, ability to prioritize, proactive, and good follow up skills.
  • IT: Usual Microsoft suite, Veeva and TMF filing programs. Medidata potentially
  • Proficient in MS Suite; Excel, Word, Outlook, Zoom, and Teams

Interested candidates should submit an updated CV.

Please click the link below to apply, or alternatively send an up to date CV to or contact me with any questions you might have.

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK***

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