Clinical Trial Manager I at Bristol Myers Squibb in Shanghai - CN
- Company: Bristol Myers Squibb
- Location: Shanghai - CN
- Posted: Sep 23, 2026
- Type: Full time
- Experience: 4+ years
- Visa sponsorship available
Overview
At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely…
Job description
- At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.
Requirements
- Thorough understanding of GCP, ICH Guidelines and Country regulatory environment.
- In depth knowledge and understanding of clinical research processes, regulations and methodology.
- Understands clinical landscape with practical knowledge of a variety of medical settings and medical records management.
- Demonstrated organizational and planning skills and independent decision-making ability.
- Strong organization and time management skills and ability to effectively manage multiple competing priorities.
- Ability of critical thinking and risk analysis.
- Strong communication skills with a strong customer focus, able to manage both internal and external clients at all organizational levels.
- Skilled in the use of technology.
- Good verbal and written communication skills (both in English and local language).
- Software that must be used independently and without assistance (Microsoft Suite, Clinical Trial Management Systems (CTMS), Electronic Data Capture Systems (eDC); Electronic Trial Master File (eTMF)).
Skills
Required
- GCP (Good Clinical Practice)
- ICH Guidelines
- Clinical research methodology
- Medical records management
- Organizational and planning skills
- Independent decision-making
- Time management
- Critical thinking
- Risk analysis
- Communication skills
- Customer focus
- Technology proficiency