Clinical Monitoring (all genders) role involves collaborating with a clinical project team, conducting IVD and MD studies, and performing various monitoring tasks.
Requirements
- University degree in biology, medicine, pharmacy or an equivalent combination of education, training and work experience in clinical trials
- At least 2 years of experience as a clinical monitor (CRA) in a CRO/medical device or pharmaceutical company
- Good knowledge of current industry practices related to the conduct of clinical studies (ICH-GCP, ISO 14155, ISO 20916)
- Good knowledge of MDR and IVDR and a good understanding of GDPR
- Ability to work independently and reliably in a fast-paced and changing environment
- Excellent communication skills in business fluent German and good written and spoken English skills are a must
Benefits
- Generous salary based on collective agreement
- Possibility of overpayment based on qualifications and experience
- Flexible work arrangement (remote or office-based)