We are currently looking for a Trainee to strengthen our Clinical Document Management team in Bremen. The successful candidate will have the opportunity to gain experience in a multidisciplinary team contributing to international clinical research projects.
The Trainee will support the management of (electronic/paper) Trial Master Files and study documentation in the context of clinical trials. This allows verification of the conduct of a clinical trial and the quality of the data generated.

Preferred qualifications:

• Completed education / work experience in an administrative area (clinical, business administration, etc.)
• Excellent planning, organizational and time management skills
• Attention to detail and the ability to work individually
• Proficient computer skills including Microsoft Word, Excel, and PowerPoint
• Proficient presentation skills (e.g. internal trainings)
• Fluency in English & German

Responsibilities:

• Assist the Clinical Document Management team
• Assist the study teams to ensure the receipt, processing and tracking of all study-related documentation
• Preparation and shipment of clinical study supplies and documents to study sites and sponsors
• Assist Project Managers and study teams in executing assigned clinical trial activities (e.g. create and maintain trackers, generate meeting minutes)
• Assist the study team in the submission of clinical trial applications to Ethic Committees and Competent Authorities

If you are interested, send us your electronic application (with your earliest start date) and your CV to:

Benjamin Tsiflidis
(Head of Clinical Document Management)
GCP-Service International Ltd. & Co.KG
Anne-Conway-Str. 2
28359 Bremen
Germany
Phone: +49 (0) 421 89676615
Fax: +49 (0) 421 4348659
E-mail: application@gcp-service.com