Clinical Trial Job Opportunity – at Bristol Myers Squibb, Apply Now
Looking for a Clinical Trial Job opportunity that lets you gain hands-on experience in global clinical studies? Bristol Myers Squibb (BMS), a global leader in biopharma, is hiring a Global Trial Acceleration Associate in Hyderabad, Telangana. This role offers exposure to clinical research jobs in Hyderabad, working across clinical documentation, regulatory submissions, site activation, and collaborative trials that transform patient lives.
- Job Position: Global Trial Acceleration Associate
- Location: Hyderabad
About The Company
At Bristol Myers Squibb, we are dedicated to transforming patients’ lives through science. Our work is challenging, meaningful, and life-changing. We offer a supportive culture that allows each employee to contribute their unique talents, fostering global participation in clinical trials. Our shared values of passion, innovation, urgency, accountability, inclusion, and integrity enable us to reach our highest potential in delivering innovative healthcare solutions.
Position Summary
The Global Trial Acceleration Associate is responsible for managing and executing centralized activities in support of global clinical trials, with a focus on clinical documentation and trial coordination. The individual interacts with clinical study sites, CROs/vendors, Country Trial Managers, study teams, and other BMS functional areas.
Key Responsibilities
- Centralized document collection, compilation, review, and approval across all clinical trial phases.
- Review and tracking of Site Monitoring Visit reports, issue escalation, and follow-up.
- Coordination with study teams for regulatory submissions, site activations, and ethical compliance.
- Supporting outsourcing activities, contracting, and execution of studies per BMS guidelines.
- Management of start-up documentation, Investigator submissions, and quality control of start-up activities.
- Updating and reviewing study-related clinical systems such as CTMS and eTMF.
- Coordination of study materials, including Investigator Site Files and pharmacy documentation.
- Ensuring ongoing communication with study teams regarding centralized study activities.
This clinical trial job opportunity is ideal for candidates seeking to advance their careers in clinical research in Hyderabad while contributing to globally impactful trials.
Essential Qualifications
- Understanding of clinical trial operations, regulatory submissions, and site documentation.
- Strong organizational, analytical, and communication skills for coordinating with multiple stakeholders.
- Ability to manage documentation, review reports, and support site activation activities independently.
- Familiarity with clinical trial management systems (CTMS, eTMF, or vendor systems) is a plus.
- Prior exposure to global clinical trials or multicenter studies is preferred but not mandatory.
Why Join Bristol Myers Squibb?
- Be part of a global biopharma leader dedicated to transforming patients’ lives through science.
- Work in a dynamic, collaborative environment where innovation, urgency, and accountability are valued.
- Gain exposure to end-to-end clinical trials, from start-up to close-out, across multiple therapeutic areas.
- Access to professional development, mentorship, and flexible work arrangements to support career growth and work-life balance.
