Attaché de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology
Core
Monitoring Phase I–IV clinical trials in oncology to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements.
Role type
Clinical Research Associate II (Oncology)
Builds
Clinical trial data and regulatory compliance for life sciences/pharmaceutical clients
Domain
Life sciences / Oncology
Required skills
Clinical trial monitoring, site management, protocol adherence, data integrity, query resolution, regulatory document collection, investigator communication, report writing
Preferred skills
Life sciences degree, bilingualism (French/English), travel availability
Technologies
EDC systems
Responsibilities
Conduct site selection, initiation, monitoring, and close-out visits; Train site personnel on study protocols and EDC systems; Ensure high-quality source documentation and timely query resolution; Oversee IP accountability and regulatory document collection; Serve as primary site contact; Prepare monitoring reports per SOPs; Support investigator meetings
Seniority
Mid-level, hands-on IC
