Bristol Myers Squibb Hiring Global Trial Acceleration Associate roles
- Bristol Myers Squibb Hiring Senior Global Trial Acceleration Associate – Clinical Trial Start-Up & Regulatory Operations | 3–5 Years Experience | Hyderabad
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Educational Qualification
- Experience
- Required Skills
- Location & Work Model
- Benefits & Work Culture
- Application Process
- Frequently Asked Questions (FAQs)
- 1. What experience is required for this role?
- 2. Is prior IRB/IEC submission experience mandatory?
- 3. Is Veeva Vault experience necessary?
- 4. Is this a remote role?
- 5. What are the career growth prospects?
- Recruitment Summary
Bristol Myers Squibb Hiring Senior Global Trial Acceleration Associate – Clinical Trial Start-Up & Regulatory Operations | 3–5 Years Experience | Hyderabad
Bristol Myers Squibb (BMS) is hiring a Senior Global Trial Acceleration Associate in Hyderabad, Telangana. This is a key role within the global clinical operations team, focused on clinical trial start-up, regulatory documentation management, IRB/IEC submissions, and electronic Trial Master File (eTMF) oversight.
This opportunity is ideal for professionals with 3–5 years of experience in clinical development, regulatory start-up, or CRO operations who are looking to advance their career within a global biopharmaceutical leader. The position supports global clinical trials from study start-up through close-out, ensuring regulatory compliance, documentation accuracy, and site activation efficiency.
Company Overview
Bristol Myers Squibb is a global biopharmaceutical company driven by a mission to transform patients’ lives through science. With a strong portfolio in oncology, immunology, cardiovascular disease, hematology, and cell therapy, BMS plays a critical role in advancing innovative therapies across multiple therapeutic areas.
The company operates globally with a strong focus on clinical research excellence, regulatory integrity, and patient-centered development. BMS clinical teams manage complex, multi-country trials designed to accelerate drug development and deliver life-changing treatments.
Working at BMS means contributing to high-impact research programs supported by advanced clinical trial technologies, global collaboration, and strict adherence to ICH-GCP and regulatory standards.
Job Role & Responsibilities
The Senior Global Trial Acceleration Associate manages centralized clinical trial activities with a strong focus on regulatory documentation, site activation, and essential document oversight.
Key Responsibilities
- Manage start-up documentation for global clinical trials, including feasibility questionnaire tracking and feedback coordination.
- Oversee submission of investigators for debarment review and track approvals.
- Review, collect, and finalize essential regulatory documents for submission to the electronic Trial Master File (eTMF).
- Act as primary contact for documentation-related activities between sites, CROs, IRBs/IECs, CTMs, and study teams.
- Support country and site activation processes, including final checklist review and regulatory submissions.
- Maintain ongoing document tracking within CTMS, eTMF, and vendor systems.
- Facilitate IRB/IEC submissions, approvals, and safety reporting activities such as SUSARs and DSUR submissions.
- Manage protocol amendments, Investigator Brochure (IB) updates, and informed consent (ICF) adaptations.
- Lead or support financial disclosure form collection and review processes.
- Coordinate certified translations of study documentation where required.
- Provide quality control oversight of study start-up documentation.
This role requires precision, compliance awareness, and the ability to manage multiple global stakeholders in a matrix environment.
Eligibility / Qualifications
Educational Qualification
Bachelor’s degree in Life Sciences, Legal Studies, Business Administration, or related field. Advanced degree is a plus.
Relevant Courses: B.Pharm, M.Pharm, Pharm.D, BSc Life Sciences, MSc Life Sciences, Biotechnology, Clinical Research, Regulatory Affairs, Biomedical Sciences, Healthcare Management, Business Administration.
Experience
- 3–5 years of clinical development or clinical operations experience in pharmaceutical, biotech, or CRO settings.
- Hands-on experience preparing and submitting regulatory documents to IRB/IECs and regulatory authorities.
- Experience managing study start-up and activation documentation.
Required Skills
- Strong knowledge of ICH-GCP guidelines and global regulatory frameworks.
- Experience with CTMS, eTMF systems (Veeva Vault preferred), and clinical trial portals.
- Ability to respond to regulatory queries effectively.
- Strong organizational, analytical, and decision-making skills.
- Effective stakeholder management in cross-functional and multicultural environments.
- Proficiency in MS Office and collaboration platforms.
- Excellent written and verbal communication skills in English.
Candidates with prior exposure to global oncology or immunology studies will have an added advantage.
Location & Work Model
Location: Hyderabad, Telangana, India
Department: Global Clinical Operations
Work Model: Site-by-design (Hybrid structure may apply as per company policy)
Benefits & Work Culture
BMS offers competitive employee benefits designed to support professional growth and work-life balance. Employees benefit from:
- Competitive salary and performance-based rewards.
- Comprehensive health insurance plans.
- Retirement planning programs.
- Global employee assistance programs.
- Inclusive and diverse workplace culture.
- Career development opportunities across global functions.
The organization maintains a strong commitment to equal opportunity employment, accessibility, and ethical business practices.
Application Process
Interested candidates can apply directly through the official BMS career portal using the link below:
Apply Here:
https://jobs.bms.com/careers/job/137477197490
Ensure your resume clearly reflects experience in regulatory submissions, clinical trial start-up, IRB/IEC coordination, and eTMF management.
Frequently Asked Questions (FAQs)
1. What experience is required for this role?
A minimum of 3–5 years of experience in clinical development or regulatory start-up within pharmaceutical, biotech, or CRO organizations.
2. Is prior IRB/IEC submission experience mandatory?
Yes. Hands-on experience in preparing and submitting regulatory documentation to IRBs/IECs is required.
3. Is Veeva Vault experience necessary?
It is preferred but not mandatory. Familiarity with CTMS and eTMF systems is essential.
4. Is this a remote role?
This is a site-by-design role, and hybrid arrangements may apply as per company policy.
5. What are the career growth prospects?
This position can lead to Global Trial Manager, Clinical Operations Lead, Regulatory Operations Manager, or Program Management roles.
Recruitment Summary
| Company | Bristol Myers Squibb |
|---|---|
| Vacancies | Senior Global Trial Acceleration Associate |
| Required Education | Bachelor’s in Life Sciences, Legal, Business or Related Field |
| Experience | 3–5 Years in Clinical Development & Regulatory Operations |
To apply for this job please visit jobs.bms.com.
