Clinical Research Jobs at BMS | Senior Trial Acceleration Associate | Life Science Jobs Apply Now
If you are searching for Clinical Research Jobs, this opportunity from Bristol Myers Squibb could be the breakthrough in your career. Through BMS Careers, the company is hiring a Senior Global Trial Acceleration Associate in Hyderabad. This role is perfect for candidates exploring Life Science Jobs and looking to work with global clinical trial teams, regulatory documentation, and trial start-up processes. Join one of the world’s leading pharmaceutical innovators and contribute to clinical research that transforms patients’ lives.
- Job Title: Senior Global Trial Acceleration Associate
- Location: Hyderabad
About the Company:
Bristol Myers Squibb is a global biopharmaceutical company focused on discovering, developing and delivering innovative medicines that help patients prevail over serious diseases. The company is known for pioneering work in oncology, immunology, cardiovascular disease, and cell therapy. Through BMS Careers, professionals in Life Science Jobs get opportunities to work on impactful global clinical trials and innovative drug development programs.
Job Details:
The Senior Global Trial Acceleration Associate plays a crucial role in supporting global clinical trials by managing centralized activities related to clinical documentation and regulatory submissions. The role involves working closely with clinical study sites, regulatory authorities, CRO partners and internal study teams to ensure smooth clinical trial start-up, site activation, documentation management and regulatory compliance. Professionals in this Clinical Research Jobs role will support trial operations throughout the study lifecycle including start-up, maintenance and close-out phases while ensuring adherence to global regulatory guidelines.
Key Responsibilities:
- Manage centralized activities supporting global clinical trials
- Maintain essential documentation within the electronic Trial Master File (eTMF)
- Coordinate with study teams, CROs and clinical trial managers
- Handle regulatory documentation submissions to IRB/IEC authorities
- Support clinical study start-up activities and site activation processes
- Track clinical trial progress using CTMS systems
- Ensure compliance with regulatory and ethical guidelines
- Manage documentation updates and communication with clinical sites
Educational Requirements:
- Bachelor’s degree in Life Sciences. Advanced degree preferred
- 3–5 years experience in clinical development, pharmaceutical, biotech or CRO industry
Skills Required:
- Knowledge of ICH-GCP guidelines and clinical research regulations
- Experience with clinical trial documentation and regulatory submissions
- Familiarity with CTMS and Veeva Vault systems
- Strong analytical, organizational and time-management skills
- Effective communication and collaboration skills
- Ability to work with cross-functional global teams
For professionals exploring Clinical Research Jobs, this opportunity through BMS Careers offers the chance to work on impactful global clinical trials and contribute to innovative drug development programs. If you are passionate about advancing healthcare and looking for high-impact Life Science Jobs, this role at Bristol Myers Squibb could be your next big career step.
