Experienced Clinical Research Associate (Oncology), Montérégie-Nord (Saint-Antoine-Sur-Ric …

Join Prevail as a Clinical Research Associate specializing in Oncology projects across Canada. Utilize your expertise in Breast Cancer studies to enhance the quality and compliance of clinical trials.

As a Clinical Research Associate, you will lead monitoring and site management for Phase I-IV oncology studies. Your role includes ensuring adherence to ICH-GCP guidelines and local regulations while working independently or remotely. You will be responsible for evaluating site performance, documentation accuracy, and establishing effective communication strategies with study sites.

Key Responsibilities:• Conduct site qualifications, monitoring, and close-out visits • Evaluate site performance and escalate serious issues timely • Maintain compliance with ICH/GCP and sponsor requirements • Verify informed consent and patient confidentiality practices • Document activities and track project metrics

Requirements:• Strong knowledge of ICH/GCP Guidelines • BS/BA in a health-related field; MS/MA desirable • Proven communication and interpersonal skills • Willing to travel up to 65% • Proficiency with computer programs like Word and Excel

Leverage your clinical expertise and contribute to impactful cancer research with Prevail. #J-18808-Ljbffr