Parexel FSP is seeking an experienced Senior CRA to oversee site management, monitoring and close-out of assigned oncology trials, ensuring patient safety and high-quality data.
The role requires extensive knowledge of ICH-GCP, FDA/local regulations, and strong collaboration with study teams, vendors and investigative sites across Europe. Minimum 3.5 years of site monitoring experience, preferably in Oncology, Vaccines or Infectious Diseases, is expected.
#J-18808-LjbffrSenior Clinical Research Associate - Oncology Site Lead employer: Parexel International
At Parexel International, we pride ourselves on being an exceptional employer, offering a collaborative and innovative work culture that empowers our employees to excel in their roles. With a strong focus on professional development, we provide ample opportunities for growth and advancement within the clinical research field, particularly in the UK and Germany, where our teams are dedicated to making a meaningful impact on patient care through cutting-edge clinical trials.
