Bristol Myers Squibb (BMS), one of the worldโs leading biopharmaceutical companies, is hiring for Global Trial Associate and Senior Global Trial Associate positions in Hyderabad, India. These clinical research jobs are excellent opportunities for candidates with experience in clinical trial management systems, eTMF, CTMS, ICH-GCP compliance, and global clinical operations.
Candidates with backgrounds in Life Sciences, Pharmacy, Clinical Research, Biotechnology, or related disciplines can apply for these exciting openings at BMS Hyderabad.
Job Details
| Particulars | Details |
|---|---|
| Company | Bristol Myers Squibb |
| Job Roles | Global Trial Associate / Senior Global Trial Associate |
| Location | Hyderabad, Telangana, India |
| Experience | 2โ4 Years |
| Qualification | BA/BS in relevant discipline preferred |
| Industry | Clinical Research / Pharma / Biotechnology |
| Employment Type | Full-Time |
| Travel Requirement | Less than 5% |
About Bristol Myers Squibb
Bristol Myers Squibb is known for transforming patientsโ lives through innovative medicines and clinical research excellence. The company offers flexible work models, global exposure, career development opportunities, and collaborative cross-functional teams across therapeutic areas.
BMS employees contribute to cutting-edge research programs while working in an inclusive and innovation-driven culture.
Global Trial Associate Responsibilities
The Global Trial Associate (GTA) role supports operational execution of global clinical trials and assists Global Trial Leads (GTLs) in ensuring studies are delivered on time, within budget, and in compliance with ICH-GCP and regulatory guidelines.
Key Responsibilities
- Support study startup, maintenance, and closeout activities
- Manage study documentation and eTMF completeness
- Assist with vendor invoice approvals and payment tracking
- Maintain global vendor site lists and study SharePoint updates
- Participate in study meetings and capture meeting minutes
- Support CTMS updates and operational planning
- Coordinate with internal and external stakeholders
- Identify risks and escalate issues appropriately
- Support study closure and archival activities
- Ensure compliance with regulatory and SOP requirements
Senior Global Trial Associate Responsibilities
The Senior Global Trial Associate position involves greater ownership of operational activities across complex global clinical trials.
Additional Responsibilities
- Independently manage GTA operational activities
- Support vendor oversight and payment tracking
- Manage protocol milestones and country planning in CTMS
- Contribute to process improvement initiatives
- Mentor junior team members and GTAs
- Support regulatory and ethics committee approvals
- Collaborate with cross-functional global teams
- Track non-clinical supplies and study deliverables
Required Qualifications
Educational Qualification
- BA/BS degree in Life Sciences, Pharmacy, Clinical Research, Biotechnology, or related discipline preferred
Experience Required
- 2โ4 years of experience in Clinical Research or related field
- Experience using:
- Clinical Trial Management Systems (CTMS)
- Clinical Trial Master File (eTMF) systems
- Knowledge of:
- ICH-GCP guidelines
- Clinical trial operations
- Regulatory processes
- Vendor and site payment tracking
Preferred Skills
- Strong communication and presentation skills
- Project management understanding
- Ability to manage multiple studies simultaneously
- Global clinical trial exposure preferred
- Stakeholder collaboration and risk management skills
Why Join Bristol Myers Squibb?
Employees at Bristol Myers Squibb receive access to:
- Global clinical research exposure
- Career growth and internal mobility
- Hybrid work opportunities
- Inclusive and collaborative work culture
- Competitive compensation and benefits
- Opportunities to work on innovative therapies
- Flexible work environment
How to Apply
Application Link For Global Trial Associate
Application Link For Senior Global Trial Associate
