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Senior Global Trial Associate

Bristol Myers SquibbHyderabad, Telangana, IndiaPosted 21 May 2026

This role at Bristol Myers Squibb involves contributing to the operational execution of clinical trials to ensure high quality and compliance. The associate will manage study-level documentation, vendor interactions, and site payments while collaborating with global cross-functional teams. Candidates must have direct clinical research experience and proficiency in industry-standard CTMS and eTMF systems. The position requires a detail-oriented professional capable of managing routine to complex trials with minimal supervision.

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Experience

2-4 years

Function

Healthcare Services

Work mode

Hybrid, India

Company

Tier 2

What you will work on

This role at Bristol Myers Squibb involves contributing to the operational execution of clinical trials to ensure high quality and compliance. The associate will manage study-level documentation, vendor interactions, and site payments while collaborating with global cross-functional teams. Candidates must have direct clinical research experience and proficiency in industry-standard CTMS and eTMF systems. The position requires a detail-oriented professional capable of managing routine to complex trials with minimal supervision.

TAL's take

Quality 65/1004/5 clarityTier 2 company

Solid role at a major global pharmaceutical firm, though specificity regarding project scale is moderate.

Role responsibilities are clearly defined within the clinical trial operational context with specific systems and compliance requirements.

Salaries at Bristol Myers Squibb

23.5 LPA average

Based on 15 Grapevine salary entries for Bristol Myers Squibb.

View all salaries

Finance

2 - 4 years | L1

12 LPA average

Range: 12 - 12 LPA

Other roles

2 - 4 years | L1

11 LPA average

Range: 7 - 18 LPA

Research

4 - 6 years | L2

21 LPA average

Range: 21 - 21 LPA

Engineering

4 - 6 years | L2

20 LPA average

Range: 20 - 20 LPA

Must haves

  • Minimum 2-4 years experience in Clinical Research
  • Knowledge of ICH/GCP and regulatory guidelines
  • Experience with Clinical Trial Management Systems
  • Experience with Clinical Trial Master File Systems

Tools and skills

clinical trial management systemsclinical trial master file systemsich/gcp guidelines

Nice to have: clinical research budgets, project management.

About the company

Global pharmaceutical company with significant clinical research operations in India.

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