Senior Clinical Trial Manager

Sourcia is a full service CRO deploying a unique model to serve our clients; small to medium-sized Bio- and Med tech. We have offices in Munich (Germany), Zevenbergen (the Netherlands) and Ghent (Belgium) and operations throughout Europe.

We believe Project Management to be one of the key success factors of a clinical trial. It determines the success or failure of a trial. Strong Project Management therefore is paramount. We put Project Management and all of its responsibilities first. It's our core business. 
To expand our team we are looking for a Senior Project Manager for the following main responsibilities associated with the job:
  • Manage efficiently study start-up, maintenance and close out phase for clinical trials in an international environment
  • Maintain ongoing contact with sponsors, vendors and project team
  • Allocation of clinical operations resources
  • Support management to external vendors
  • Manage Timeline and Budget
  • Study Status Oversight and Tracking
  • Oversee and lead CRAs and Coordinators


  • At least 5 years of international Project Management experience in clinical research
  • In-depth experience of clinical trial processes
  • Ability to successfully develop, implement, manage and complete international clinical trials
  • Thorough knowledge of FDA and EMEA regulations, ICH GCP and associated EU Directives governing the conduct of clinical trials
  • Experience in management of external resources and vendor relations
  • Ability to work in cross-functional, multi-national teams
  • Experience in preparation and participation in business development activities, such as General Capabilities and Bid Defense Meetings
  • Training and development of junior level Project Managers
  • Excellent interpersonal skills
  • Ability to work independent and unsupervised


The ideal candidate will align with Sourcia’s culture and drive by being accountable for their work with honesty, uprightness, attention to detail and taking pride in what we do.

To apply for this role or for more information, please contact us at