Clinical Project Coordinator

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 are growing and are looking for new colleagues at our offices in Munich as well as Zevenbergen:

Clinical Project Coordinator

As Clinical Project Coordinator (f/m/n) you are an important component of the research team. You are working side by side with the responsible Project Manager to organize and manage all aspects in the conduct of our international clinical trials. 

 

Work activities include:

Your profile:

       Supporting Project Management in all aspects of the project execution

       Preparing and Attending investigator meeting(s)

       Developing and maintaining the study budget and verify all costs

       Preparing for study initiation

       Maintaining study files (Trial Master File)

       Tracking and maintaining the study budget and timelines

       Preparation of study specific templates

       Maintaining communication and correspondence with all parties involved

       Degree in Life Science or equal experience in clinical development / monitoring

       Excellent interpersonal skills to deal effectively with clinicians, patients, administrators, auxiliary personnel, regulators, monitors and sponsors

       Knowledge of medical terminology

       Knowledge of ICH-GCP and industry standards

       Familiarity with Microsoft Office 

       Excellent organizational skills to independently manage work flow

       Ability to prioritize quickly and appropriately

 

 

We are looking forward hearing from you – please send your application to info@sourcia.eu

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