Global Trial Acceleration Associate Job in Hyderabad at Bristol Myers Squibb, documentation, site activation, and regulatory processes at BMS.
About the Company
Bristol Myers Squibb (BMS) is a leading global biopharmaceutical company with a single, powerful vision: Transforming patients’ lives through science™. At BMS, employees work on uniquely meaningful and life-changing innovations across oncology, hematology, cardiology, immunology, and other therapeutic areas.
BMS fosters a culture of inclusion, integrity, innovation, and accountability, empowering employees to grow professionally while making a real impact on patients worldwide. With a strong focus on flexibility, well-being, and career development, BMS offers opportunities that go far beyond traditional roles.
Job Details
- Job Title: Global Trial Acceleration Associate
- Job Requisition ID: R1595205
- Job Type: Full-Time
- Location: Hyderabad, Telangana, India
- Work Model: Site-by-design / On-site as per BMS occupancy protocol
- Department: Clinical Development / Global Clinical Operations
Job Description
Bristol Myers Squibb is hiring a Global Trial Acceleration Associate to support centralized operational activities for global clinical trials, with a strong emphasis on clinical documentation and study start-up processes. Global Trial Acceleration Associate Job
This role works closely with global study teams, clinical trial sites, CROs, vendors, and internal stakeholders to ensure smooth execution of study start-up, maintenance, and close-out activities. The position plays a key role in document management, ethical and regulatory submissions, and site activation activities across regions. Global Trial Acceleration Associate Job
Key Responsibilities
- Manage and execute centralized activities supporting global clinical trials, with focus on essential clinical documentation
- Serve as a primary point of contact for document management and ethical/regulatory submission activities
- Coordinate with clinical sites, CROs, vendors, CTMs, CTMos, and study teams throughout the trial lifecycle
- Initiate and manage start-up documentation for global clinical trials
- Support country and site activation activities, including final review and sign-off of activation checklists
- Submit potential investigators for debarment review and track decisions
- Maintain and track essential documents throughout study start-up, maintenance, and close-out phases
- Update and review clinical trial systems such as CTMS, eTMF, and vendor platforms
- Provide quality control support for study start-up activities
- Coordinate certified translations of study documents such as ICFs, protocols, and investigator brochures
- Assist with preparation of investigator site files and pharmacy materials
- Review site monitoring visit reports centrally and manage issue escalation and follow-up
- Support CSR distribution and country/site-level ICF adaptations
- Create and manage standardized document templates as required
- Communicate regularly with study teams on centralized trial activities
- Perform additional duties to support global clinical trials as assigned
Global Trial Acceleration Associate Job
Skills / Qualifications
Educational Qualifications
- Bachelor’s degree in Life Sciences, Legal, Business Administration, or related field
- Advanced degree is an advantage
Experience Requirements
- Minimum 3 years of clinical development or operational experience in pharmaceutical, biotech, CRO, or related fields
- Prior experience as a Clinical Research Associate (CRA) with global monitoring exposure is preferred
- Experience reviewing CRA monitoring reports is strongly preferred
Technical & Professional Skills
- Hands-on experience preparing, reviewing, and submitting regulatory documents to IRBs/IECs and regulatory authorities
- Experience with study start-up and site activation documentation
- Strong knowledge of ICH-GCP guidelines and regulatory requirements
- Familiarity with CTMS, eTMF, Veeva Vault (preferred), SharePoint, and MS Office tools
- Understanding of the drug development process and clinical trial operations
- Strong organizational, analytical, and time-management skills
- Excellent written and verbal communication skills in English
- Ability to work effectively in cross-functional, multicultural, matrix environments
- Proven stakeholder management and collaboration skills
- High adaptability to complex, fast-changing work environments
Global Trial Acceleration Associate Job
Benefits / Perks
- Competitive compensation and benefits package
- Flexible and balanced work environment
- Career development and internal growth opportunities
- Exposure to global clinical trials and cross-functional teams
- Employee wellness programs and support services
- Inclusive workplace with strong focus on diversity and accessibility
Global Trial Acceleration Associate Job
Why You Should Join
At Bristol Myers Squibb, your work directly contributes to advancing science and improving patient lives. Employees are empowered to bring their unique perspectives, collaborate globally, and grow through challenging and meaningful work.
BMS offers not just a job, but a long-term career built on purpose, innovation, and continuous learning in a supportive and inclusive environment. Global Trial Acceleration Associate Job
On-Site Work Protocol
This role follows BMS’s site-by-design occupancy model, requiring significant on-site presence to support collaboration, innovation, and operational excellence. The exact work arrangement depends on role responsibilities and business needs. Global Trial Acceleration Associate Job
Supporting People with Disabilities
Bristol Myers Squibb is committed to equal employment opportunity and providing reasonable workplace accommodations throughout the recruitment and employment process. Global Trial Acceleration Associate Job
How to Apply
Applicants are encouraged to apply even if their experience does not perfectly match every requirement.
FAQs
Is this a full-time role?
Yes, this is a full-time permanent position.
Is prior CRA experience required?
CRA experience is preferred, especially with global site monitoring exposure, but not mandatory.
What systems experience is required?
Experience with CTMS, eTMF, and clinical trial systems is required. Veeva Vault experience is preferred.
Is this a remote role?
No. This role follows BMS’s site-based or hybrid work model depending on business needs.
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