Clinical Trial Registration Sr. Specialist | BMS Careers in Clinical Data Management
Transform your career with Bristol Myers Squibb (BMS) — where science meets purpose. The company is seeking a Clinical Trial Registration Sr. Specialist within its Global Development Operations team. This opportunity is perfect for professionals aiming to excel in clinical data management jobs and make a global impact through transparent and efficient clinical research. Join BMS, a world leader in biopharmaceutical innovation, and elevate your future with one of the most respected names in clinical research jobs and BMS careers.
About the Company:
Bristol Myers Squibb (BMS) is a leading biopharmaceutical company driven by its mission to “Transform patients’ lives through science™.” Across departments and continents, BMS delivers groundbreaking advancements in oncology, cardiovascular, immunology, and fibrosis. Every member of the BMS careers community contributes to life-changing innovations while enjoying a culture that values inclusion, accountability, and collaboration. With world-class benefits, flexible work models, and cutting-edge projects, BMS empowers professionals pursuing clinical research jobs to grow and thrive globally.
Job Details:
The Clinical Trial Registration Sr. Specialist plays a key role in ensuring compliance, transparency, and accuracy in clinical data management and trial registration activities. This role involves supporting
the registration and maintenance of clinical trials in public registries across multiple regions including the US and EU.- Division: Research & Development
- Functional Area: Global Development Operations / Trial Delivery Support / Trial Risk and Integrity Management
- Location: India (Hybrid)
Key Objective: Provide operational support for clinical trial registration, ensuring high-quality, compliant data disclosure aligned with regulatory guidelines.
Educational Requirements:
- Bachelor’s degree in a science-related field (Life Sciences preferred).
- Strong foundation in clinical research principles, data integrity, and regulatory compliance.
Key Responsibilities:
- Manage registration and maintenance of clinical trials on platforms such as ClinicalTrials.gov and EU PAS.
- Collaborate with cross-functional teams including trial managers, statisticians, and medical experts.
- Ensure clinical trial data accuracy and regulatory adherence for global submissions.
- Update study trackers and ensure weekly reporting compliance.
- Educate team members on NIH and protocol registration guidelines.
- Support registration of clinical research trials beyond US/EU as required.
Skills Required:
- Strong analytical, Excel, and data validation skills.
- Excellent written and oral communication abilities.
- Ability to manage multiple studies and timelines efficiently.
- Strong understanding of clinical data management systems.
- Proven experience in clinical research or regulatory documentation.
- Capability to work independently and cross-functionally in global teams.
Step into the world of clinical data management jobs at Bristol Myers Squibb — where each project helps transform lives through science. Whether you’re advancing data quality or ensuring trial transparency, every task contributes to a larger mission. Build your career with BMS careers and become part of a global legacy in clinical research jobs that truly make a difference.
