Bristol Myers Squibb Hiring Global Trial Acceleration Associate roles
- Life Science Global Trial Acceleration Associate Opening Hyderabad
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Required Education
- Relevant Courses (comma-separated)
- Required Experience
- Skills Needed
- Location & Salary
- Application Process
- FAQs
- Who can apply for this role?
- Is CRA experience mandatory?
- Does this role involve regulatory submissions?
- What systems should I know?
- Is global experience required?
- Is remote work allowed?
- Summary Table
Life Science Global Trial Acceleration Associate Opening Hyderabad
Apply for Global Trial Acceleration Associate roles in Hyderabad. Life science graduates with 3+ years clinical research experience eligible.
Bristol Myers Squibb is hiring experienced clinical research professionals for the Global Trial Acceleration Associate position in Hyderabad. This role is suited for candidates who can support global clinical trial operations, manage essential documentation, coordinate with study teams, and ensure regulatory compliance across multiple study phases. If you have hands-on experience with study start-up, site activation, and documentation management, this is a chance to join one of the world’s most respected biopharmaceutical organizations.
Company Overview
Bristol Myers Squibb (BMS) is a leading global biopharmaceutical company focused on transforming patients’ lives through science. With a strong commitment to innovation, BMS advances therapeutic breakthroughs across oncology, immunology, hematology, and cardiovascular disease. The company offers an environment where meaningful work meets unmatched growth opportunities, along with a culture built on passion, accountability, inclusion, and scientific excellence.
Job Role & Responsibilities
The Global Trial Acceleration Associate supports global study teams across start-up, maintenance, and close-out activities. The role involves document management, site activation, vendor coordination, and regulatory submissions.
Key Responsibilities
- Manage centralized activities for global clinical trials with focus on essential documentation
- Interact with study sites, CROs, vendors, CTMs, CTMos, and multiple BMS functional teams
- Support outsourcing activities including vendor selection, contracting, and compliance checks
- Initiate and manage start-up documentation for global clinical trials
- Submit potential investigators for debarment review and track outcomes
- Oversee country and site-level activation activities, including final documentation checks
- Maintain and update clinical systems (CTMS, eTMF, Veeva Vault, vendor systems)
- Coordinate certified translations for study-level documentation when required
- Assist with creation of study-specific materials (Investigator Site Files, pharmacy files)
- Review and maintain essential documentation across all trial phases
- Perform centralized review of Site Monitoring Visit reports and escalate issues
- Support CSR distribution and document template management
- Communicate regularly with study teams on centralized study activities
Eligibility / Qualifications
Required Education
- Bachelor’s degree in Life Sciences, Legal, Business Administration or equivalent
- Advanced degree preferred
Relevant Courses (comma-separated)
B.Sc Life Sciences, M.Sc Life Sciences, B.Pharm, M.Pharm, B.Sc Nursing, B.Sc Biotechnology, M.Sc Biotechnology, Clinical Research Certification, PG Diploma Clinical Research.
Required Experience
- Minimum 3 years in clinical development operations within pharma, biotech, or CRO
- Experience as field monitor/CRA with global monitoring exposure preferred
- Strong understanding of ICH-GCP and global regulatory guidelines
- Hands-on experience preparing, reviewing, and submitting IRB/IEC and regulatory documentation
- Experience in clinical study start-up, activation, and response handling
Skills Needed
- Strong organizational, analytical, and decision-making capabilities
- Effective communication (written and verbal) in English
- Proficiency in MS Office, SharePoint, CTMS, eTMF, Veeva Vault, and other trial systems
- Ability to work in a matrix structure with multiple stakeholders
- Strong coordination, time management, and adaptability
Location & Salary
- Location: Hyderabad, Telangana (Onsite/Hybrid depending on role classification)
- Salary: Competitive, based on experience, therapeutic expertise, and system proficiency
BMS offers comprehensive benefits including health coverage, retirement plans, flexible work options, and career development programs.
Application Process
Apply directly through the official BMS careers portal.
Apply Here: https://jobs.bms.com/careers/job/137477197485
Prepare a detailed CV highlighting your experience in:
- Clinical trial operations
- Study start-up and site activation
- Essential documentation management
- Regulatory submissions
- Experience with CTMS/eTMF systems
FAQs
Who can apply for this role?
Life science graduates with 3+ years of clinical research or operations experience.
Is CRA experience mandatory?
Not mandatory but strongly preferred.
Does this role involve regulatory submissions?
Yes. The role includes preparation, review, and submission of IRB/IEC documents.
What systems should I know?
CTMS, eTMF, Veeva Vault, and general clinical trial management systems.
Is global experience required?
Experience working across multi-country studies or with global teams is preferred.
Is remote work allowed?
Depends on role type; some are hybrid or onsite as per BMS policy.
Summary Table
| Category | Details |
|---|---|
| Company | Bristol Myers Squibb, Hyderabad |
| Vacancies | Global Trial Acceleration Associate |
| Required Education | Life Sciences, Pharmacy, Biotechnology, Nursing, Business Administration |
| Experience | Minimum 3 years in clinical development, CRA/monitoring preferred |
To apply for this job please visit jobs.bms.com.
