Bristol Myers Squibb hiring Global Trial Associate
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Required Education
- Experience Requirement
- Required Skills
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- Is this role suitable for freshers?
- Is this a project management role?
- What systems knowledge is preferred?
- Is the role hybrid or onsite?
- What is the career progression after this role?
- Job Summary Table
Bristol Myers Squibb hiring Global Trial Associate in Hyderabad. Clinical research professionals with 2–4 years experience eligible. Hybrid role.
Bristol Myers Squibb (BMS) is hiring a Global Trial Associate for its clinical research operations team in Hyderabad, India. This role is designed for clinical research professionals who want to work on global clinical trials, support study execution, and gain exposure to international regulatory standards. The position offers a hybrid work model and the opportunity to contribute directly to life‑changing clinical research programs across therapeutic areas.
Company Overview
Bristol Myers Squibb is a global biopharmaceutical company focused on discovering, developing, and delivering innovative medicines for patients with serious diseases. With a strong presence across oncology, immunology, cardiovascular, and cell therapy research, BMS is recognized worldwide for its science‑driven culture and patient‑first values.
BMS India plays a critical role in global clinical development, regulatory operations, and data‑driven trial execution. The organization is known for its strong compliance culture, adherence to ICH‑GCP standards, and commitment to inclusive, ethical clinical research practices.
Job Role & Responsibilities
As a Global Trial Associate (GTA), you will support global clinical trials through operational execution, documentation oversight, and coordination with cross‑functional teams. The role blends project management support with hands‑on trial operations.
Key Responsibilities
- Support the Global Trial Lead (GTL) in driving study execution using performance metrics and quality indicators
- Assist in study planning, conduct, maintenance, and close‑out activities
- Manage study‑level documentation and ensure accuracy and completeness of the electronic Trial Master File (eTMF)
- Review vendor invoices, manage accruals, and support SOW and budget changes
- Coordinate vendor creation, payment processing, and global vendor site lists
- Support startup, maintenance, and closure phases of clinical studies
- Maintain study SharePoint sites, mail groups, and study directories
- Participate in study team meetings, prepare agendas, and capture meeting minutes
- Identify operational risks and issues, develop mitigation plans, and escalate appropriately
- Support filing activities, audits, and study archival during closure phase
- Assist with clinical study report (CSR) appendices as required
This role plays a key part in ensuring clinical trial quality, compliance, and timely delivery of study milestones.
Eligibility / Qualifications
Required Education
Candidates should hold one of the following qualifications:
Life Sciences, Pharmacy, Clinical Research, Biotechnology, Biology, Healthcare‑related Degrees
Experience Requirement
- 2 to 4 years of experience in clinical research or clinical trial operations
- Hands‑on experience with Clinical Trial Management Systems (CTMS) and eTMF platforms preferred
- Exposure to global clinical trials is an added advantage
Required Skills
- Working knowledge of ICH‑GCP guidelines and global regulatory requirements
- Basic understanding of clinical research budgets and vendor payment processes
- Strong project coordination and documentation skills
- Excellent written and verbal communication abilities
- Ability to collaborate with global, cross‑functional stakeholders
- Strong attention to detail and compliance mindset
Location & Salary
- Job Location: Hyderabad, Telangana, India
- Work Model: Hybrid (#LI‑Hybrid)
- Employment Type: Full‑time
Application Process
Interested candidates can apply directly through the official Bristol Myers Squibb careers portal:
Apply Online: https://jobs.bms.com/careers/job/137478325661
Candidates are encouraged to apply even if their experience does not match every requirement, as BMS values diverse backgrounds and potential.
Frequently Asked Questions (FAQs)
Is this role suitable for freshers?
No. This role requires prior experience in clinical research or trial operations.
Is this a project management role?
This is a clinical trial operations support role with project coordination responsibilities.
What systems knowledge is preferred?
Experience with CTMS and eTMF systems is preferred.
Is the role hybrid or onsite?
This position follows a hybrid work model based in Hyderabad.
What is the career progression after this role?
Career growth includes Senior Global Trial Associate, Clinical Trial Manager, and Global Study Operations roles.
Job Summary Table
| Company | Bristol Myers Squibb |
|---|---|
| Vacancies | Global Trial Associate |
| Required Education | Life Sciences, Pharmacy, Clinical Research, Biotechnology, Biology |
| Experience | 2–4 Years |
To apply for this job please visit jobs.bms.com.
