Clinical Research Associate (CRA)

AurigaVision AG seeks a mid-level Clinical Research Associate for hybrid work in Zürich. The role focuses on Phase II/III oncology trials, requiring 50% travel across Switzerland and Europe to monitor sites and ensure regulatory compliance.

This position supports Phase II and III oncology studies by overseeing clinical trial sites across Switzerland and Europe. The specialist ensures that all research activities adhere to established protocols and regulatory standards while maintaining strong partnerships with site personnel to drive patient enrollment.

Responsibilities

• Oversee clinical trial locations to verify adherence to GCP, ICH standards, and study protocols.
• Conduct site initiation, interim monitoring, and close-out visits for Phase II/III oncology trials.
• Examine and validate source data, case report forms, and informed consent documentation.
• Establish strong relationships with investigators and site staff to ensure enrollment targets are met.
• Identify and escalate protocol deviations and safety concerns in a timely manner.

Requirements

• Bachelor's or Master's degree in Life Sciences, Nursing, or Pharmacy.
• 3-5 years of clinical monitoring experience, preferably in oncology.
• Thorough knowledge of ICH-GCP, local regulations, and clinical trial processes.
• Excellent organizational skills and ability to manage multiple sites simultaneously.
• Willingness to travel up to 50% within Switzerland and Europe.

Nice to have

• preferably in oncology