Beschreibung
Our client, a Global pharmaceutical company in the greater Frankfurt area, is currently looking for a Pharmacovigilance Specialist to support the Pharmacovigilance Department for approx. 6 months. There is the possibility to work as a freelancer or in a fix term contract (through our company Sthree Temp Experts GmbH).Your will be responsible for:
- Review of adverse event information received by the company worldwide from clinical trials, licence partners and spontaneous reports
- Ensure collected adverse drug events are processed according to global SOPs / Working Instructions and international regulatory guidelines
- Support reconciliation with the clinical database
Requirements:
- Medical documentation officer or assistant or comparable skills
- Knowledge of medical terminology
- Working knowledge in Pharmacovigilance
- Good skills in working with databases and Office Software
- Good communication skills, reliability ability to work within a team
- Advanced knowledge of English including medical terminology. Basic German
LOCATION: RHEIN-MAIN
DURATION: Sept. 2017 - March 2018
CAPACITY: 100% available
Should you have interest in applying, please apply with your CV in English and we will be in contact with you should you fit the above requirements. Please note that only applications submitted complete with CV will be considered.
Sthree Germany is acting as an Employment Business in relation to this vacancy.