Clinical Trial Manager (m/f)

Job type:
12 MM++
Hays AG
Basel region
flag_no Switzerland
Contact person:
Kerstin Werner
project ID:

This project is archived and not active any more.
You will find vacant projects in our project database.

Clinical Trial Manager (m/f)

Reference: en
Start: asap
Duration: 12 MM++

Main tasks:
  • Responsible for supporting the operational management and oversight of clinical trials within assigned countries/regions
  • Work closely with Clinical Development Operations trial team to support clinical trial-related activities at the country/site level
  • Manage various aspects of the collaboration with external service providers for clinical services, may participate in the selection of External Service Providers (ESPs) and training of ESP Personnel, contribute to the completion of ESP scope documents and applicable ESP documents (e.g., lab manuals)
  • Oversee performance of ESPs on a global level to ensure compliance with the clinical study protocol and in accordance with the scope of work (SoW)
  • Contribute to the development and updating of clinical trial-related risk mitigation and contingency plans, and proactively identify new risks
  • Support submission to Health Authorities and Independent Ethics Committees/Institutional Review Boards (IECs/IRBs) and perform ongoing quality checks/reviews of the (e)TMF(s) and ensure audit readiness in assigned area of Responsibility

Main qualifications
  • Bachelor's degree or equivalent university education/degree, preferably in life sciences or healthcare
  • Experience performing clinical trial management activities with experience in Phase 2 and 3
  • Detailed understanding of International Council for Harmonization - Good Clinical Practice (ICH-GCP) including international regulatory requirements for the conduct of clinical development programs in key regions (Americas, Europe, Asia Pacific, and Australia)
  • Experience in managing External Service Providers (ESP) including performance assessments and finance management (invoice review, change order management, budget reforecasting, etc.)
  • Previous experience working with electronic data capture systems (EDCs), electronic Trial Master Files (eTMFs), and Clinical Trial Management Systems (CTMSs) is preferred
  • Fluency in English and available to travel domestically and internationally

Main advantages:
  • Pleasant working atmosphere

About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.