Senior Clinical Research Associate - pharma

• Monitoring clinical studies in phases II-III in Switzerland & Austria
• Assuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures.
• Identification, qualification and initiation of investigators and their sites.
• Supervising study conduct according to GCP requirements and all applicable laws.

Key Requirements

• Bachelor degree in life-science
• Min 1.5 years of monitoring experience as CRA / Clinical Research Associate within a CRO, Pharma, Biotech
• Experience with site initiation, site close out
• Experience in clinical studies phase II-III
• FTE: 1.0