Offer summary
Qualifications:
Degree in natural sciences (Biology, Chemistry, Medicine, Pharmacy), Certification as Clinical Research Associate (CRA), Experience in clinical or medical research preferred, Knowledge of regulatory requirements including ICH-GCP, Fluent English (C1) and MS Office proficiency.Key responsabilities:
- Monitor mono- and multi-center clinical studies
- Conduct feasibility studies and process optimization
- Communicate with study centers and external partners
- Create and maintain study-specific documentation
