Attaché de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Domain
Clinical Research / Oncology
Seniority
Mid-Senior level (CRA II)
Required skills
French, English, Clinical trial monitoring (Phase I-IV), GCP/ICH compliance, Site selection, Site initiation, Site monitoring, Site close-out, Protocol training, EDC systems, Source documentation review, Query resolution, Regulatory document collection, Investigator meetings
Preferred skills
Bachelor's degree in Life Sciences or related discipline
Responsibilities
Conduct site selection, initiation, monitoring, and close-out visits; Train site personnel on study protocols, EDC systems, and study requirements; Ensure high-quality source documentation, data integrity, and timely query resolution; Oversee IP accountability and regulatory document collection; Serve as the primary site contact and maintain regular communication; Prepare monitoring reports following SOPs and timelines; Support investigator meetings and collaborate with CTMs/Lead CRAs
Technologies
EDC systems
