Clinical Research Associate II
Bristol Myers Squibb · Shanghai, China
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
This Clinical Research Associate II role focuses on maintaining data integrity and conducting monitoring activities across clinical trials. Responsibilities include tracking records, inventory assessments, supporting audits and corrective actions, and managing study budgets. The position is site-by-design and based in Shanghai.
What they're looking for
- Experience maintaining clinical trial site tracking records and relevant guidelines
- Knowledge of clinical monitoring plans and investigational product assessment procedures
- Familiarity with audit, inspection activities, and corrective/preventive action processes
- Experience with study budget preparation and clinical study agreements
- Ability to support process improvement and operational efficiency initiatives
What you'll be doing
- Maintain integrity of clinical data through site tracking records and guideline compliance
- Execute monitoring activities according to approved monitoring plans
- Conduct physical inventory and records review of investigational products
- Support audit and inspection activities while leading issue resolution and corrective actions
- Assist with study budget preparation, clinical study agreements, and payment processing
Privacy & handoff
This role links to Bristol Myers Squibb's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.