Clinical Research Associate (CRA)
Oncology focus – travel required (50%)
For our client, a leading pharmaceutical company based in Switzerland, we are looking for a
Clinical Research Associate (CRA) 100% (Ref. Nr. 3002)
Oncology focus – travel required (50%)
Your main tasks
Monitor clinical trial sites to ensure compliance with GCP, ICH guidelines, and study protocols.
Perform site initiation, interim monitoring, and close-out visits for Phase II/III oncology trials.
Review and verify source data, case report forms, and informed consent documentation.
Build 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.
Your profile
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.
