Clinical Operations Manager

  • Salary: CHF70 - CHF77 per hour
  • REF Number: v-129438
  • Consultant: Hendre Moolman
  • Contact: 01438842970
  • Date Published: 09.04.2025
  • Industry: Pharmaceutical
  • Location: Basel, Switzerland
  • Functional Expertise: Clinical Operations/Development

Job Title: Clinical Operations Manager

Location: Basel

Salary: Up to 70.00CHF per hour

CK QLS are recruiting for a Clinical Operations Manager, to join a growing biopharmaceutical company, at their site based just outside of Basel, in Allschwil. The position is offered on a 12 month contract with the possibility of extension.

Clinical Operations Manager Role:

  • Driving the development of the operational trial related documents and procedures, as well as setting-up the Service Providers.
  • Overseeing the deliverables of all Service Providers related activities, from specifications to close-out.
  • Managing the operational trial related activities in close collaboration with other functions.

Further Responsibilities will Include:

  • Leading the development of ESP specifications, testing and implementation in collaboration with other functions, and ensure appropriate quality control of deliverables.
  • Supervising the deliverables towards the Contract Research Organization (CRO) and Service Providers selected for the trial, to ensure compliance with study protocol.
  • Contribute to the Study Master File (StMF) completeness and readiness for audit/inspection and by performing ongoing quality checks/review.

Your Background:

  • Bachelor of Science degree or equivalent University degree in life sciences or healthcare.
  • 4 years of experience in managing operational aspects of Phase II and Phase III trials and executing a wide range of clinical trial activities from study start up to clinical study report.
  • Experience in working in global cross-functional (matrix) and multicultural teams.
  • Experience in selecting and managing External Service Providers (ESP).
  • Previous experience working with electronic data capture, electronic Trial Master File (eTMF), and Clinical Trial Management Systems (CTMS).
  • Excellent knowledge of International Conference on Harmonization-Good Clinical Practice (ICH-GCP) guidelines.

This is an excellent opportunity to join a growing biopharmaceutical company.

Apply:

Please could you send any correspondence in English. Please quote job reference 129 438 in all correspondence. It is essential that applicants hold entitlement to work in Switzerland.

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