Parexel

UK Clinical Trial Manager – CRO Oversight – FSP

Parexel

full-time

Posted on:

Location Type: Remote

Location: United Kingdom

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About the role

  • Manage integration of project team activities
  • Manage strategic study operations including study sites and tracking systems for regulatory submissions
  • Provide input on trial level operational strategies for clinical trials
  • Manage aspects of CRO/vendor identification and day-to-day operational management activities of CROs and other vendors

Requirements

  • Bachelor’s or nursing degree or equivalent required, science preferred
  • Minimum 5+ years of clinical research experience with a CRO, biotech or pharmaceutical company
  • 2-3 years leading aspects of clinical trials
  • CRO oversight experience is essential
Benefits
  • Competitive salary
  • Flexible working hours
  • Health insurance
  • Professional development opportunities
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
clinical researchregulatory submissionsoperational strategiesCRO managementvendor managementstudy operationstrial management
Soft Skills
leadershiporganizational skillscommunication
Certifications
Bachelor’s degreenursing degree