Bristol Myers Squibb (BMS), a global leader in biopharmaceutical innovation, is hiring a Global Trial Acceleration Associate in Hyderabad, Telangana. This role offers a unique opportunity to support clinical trials worldwide, ensuring smooth regulatory submissions, essential document management, and site activations. If you’re passionate about clinical research and want to contribute to life-changing science, this could be your next career move.
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Key Responsibilities
As a Global Trial Acceleration Associate at BMS, you will:
- Manage and execute centralized activities for global clinical trials.
- Act as the main point of contact for essential document management, regulatory, and ethical submissions.
- Support outsourcing activities including vendor selection, contracting, and execution of outsourced studies.
- Initiate and manage start-up documentation activities.
- Conduct debarment reviews for potential investigators.
- Handle site activation checklists and approvals.
- Ensure quality control of start-up activities and essential documentation.
- Update and review clinical systems (CTMS, eTMF, Veeva Vault).
- Coordinate certified translations and investigator site files.
- Review monitoring visit reports, escalate issues, and follow-up as required.
- Assist in CSR distribution and ICF adaptations.
Qualifications & Experience
- Education: Bachelor’s degree in Life Sciences, Legal, Business Administration, or related field (advanced degree a plus).
- Experience: Minimum 3 years in clinical development, operations, or site monitoring.
- Preferred experience in Oncology, Cardiology, Hematology, or Immunology.
- Strong knowledge of ICH/GCP, drug development, and regulatory guidelines.
- Proficiency in CTMS (Veeva Vault preferred), eTMF, SharePoint, MS Office.
- Strong communication, organizational, and time-management skills.
- Ability to manage stakeholders and work in a cross-functional, multicultural environment.
Benefits at BMS
- Competitive compensation and benefits package.
- Career growth opportunities in global clinical trial operations.
- Exposure to cutting-edge research in multiple therapeutic areas.
- Hybrid work model (site-by-design).
- Inclusive and supportive workplace culture.
How to Apply
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