Job Description
Our range
- Support of study participants according to the study protocol and documentation of study data in appropriate systems
- Organization and implementation of study visits in cooperation with the investigators
- Support with initiations, monitoring visits, audits and regulatory inspections
- Close cooperation with the investigators in the implementation of the study protocols
- Archiving of study documents according to legal and customer-specific requirements.
Your strengths
- Completed medical training and experience in clinical trials
- Ideally additional qualification as a study nurse and knowledge of Good Clinical Practice (GCP) and the German Medicines Act
- Very good written and spoken English skills
- Good MS Office skills
- Dedicated, independent working style, high organizational skills and a friendly, empathetic approach to patients.
Your benefits
- Remuneration according to TVöD/VKA, supplemented by a company pension scheme
- Further training and continuing education opportunities for professional and personal development
- Further benefits such as our subsidy for the Deutschlandticket, bicycle leasing, our offers for balancing work and family life as well as our company health management can be found at What we offer | Health North Hesse .
Interested?
Your contact person for questions:
Tanja Reuter
Head of Coordination Office
for Central Study Management
0561 980 – 3504
tanja.reuter[at]gnh.net