Clinical Research Associate: Site Monitor & Compliance
Bristol Myers Squibb EU Policy
Bristol Myers Squibb is seeking a Clinical Research Associate (CRA) for the Ohio region to monitor trial sites, ensure protocol compliance, and uphold data integrity across all phases. This role requires collaboration with cross-functional teams and external partners, with potential travel up to 70%. The candidate should have 2-3 years of clinical research experience, a life sciences degree, and familiarity with ICH/GCP guidelines. #J-18808-Ljbffr Bristol Myers Squibb EU Policy
Vacancy posted 1 day ago
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