Bilingual Clinical Research Associate (CRA) – Clinical Research Coordinator Experience
Core
Conduct on-site monitoring visits for clinical trials to ensure data integrity and regulatory compliance across various therapeutic areas.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data and regulatory compliance for biotechnology, pharmaceutical, and medical device companies
Domain
Clinical Research / Life Sciences
Required skills
Clinical trial monitoring, GCP/ICH E-6 compliance, patient chart review, site correspondence, database management, travel logistics, regulatory knowledge (Health Canada)
Preferred skills
Experience in oncology, cardiology, or metabolic areas
Technologies
CTMS, Microsoft Office (via careerplan.io/jobs/12672-bilingual-clinical-research-associate-cra-clinical-research-coordinator-experience-at-medp)
Responsibilities
Conduct pre-study, initiation, monitoring, and closeout visits; Maintain site files and correspondence; Review patient charts and clinical data; Complete visit reports; Interact with research sites
Seniority
Mid-level, hands-on IC