We are currently seeking a Safety Data Coordinator to join our established Drug Safety Department in Mannheim, Germany.
The Safety Data Coordinator leads the development and implementation of medical coding in clinical data management systems, participates in management of individual case safety reports (SAEs, AEs of Special Interest, Adverse Drug Reactions), AE/SAE reconciliation and data retrievals from the clinical and/or safety databases and provides support for endpoint adjudication committees.
The ideal candidate will have experience in medical documentation or an undergraduate degree (or equivalent) preferably within life sciences, with the ability to read, understand and summarize medical source documents.
You should have a keen interest in drug and ideally clinical safety.
An understanding of regulations relevant to safety of drugs in development and post authorizations as well as knowledge of clinical research would be an advantage, but not mandatory.
Fluency in English and a good level of German is required.
Previous experience using computerized information systems and standard application software (Windows, MS Office) is preferred.
For further information please contact me via Xing or email directly to me!
Anne Becker-Roskowetz, Dipl.-Betriebswirtin (FH)
Recruiter – Global Talent Acquisition