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Bristol Myers Squibb Hiring Global Trial Associate

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Bristol Myers Squibb (BMS)

degree in Life Sciences, Pharmacy, Biotechnology, Nursing, Clinical Research, or a related discipline preferred.

Hyderabad, Telangana, India

2–4 years

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Global biopharmaceutical leader Bristol Myers Squibb (BMS) has announced an exciting opportunity for experienced clinical research professionals. The company is hiring a Senior Global Trial Associate (GTA) in Hyderabad, India. This clinical operations role offers the opportunity to work on global clinical trials, collaborate with cross-functional teams, and contribute to the development of innovative therapies that transform patients’ lives.

Professionals with experience in clinical research, clinical trial management systems (CTMS), eTMF management, and global trial operations are encouraged to apply.

Job Overview

  • Position: Senior Global Trial Associate
  • Company: Bristol Myers Squibb (BMS)
  • Location: Hyderabad, Telangana, India
  • Job Type: Full-Time
  • Requisition ID: R1600982
  • Experience Required: 2–4 Years
  • Industry: Clinical Research / Pharmaceutical / Biotechnology

Key Responsibilities

The Senior Global Trial Associate will support the operational execution of global clinical studies while ensuring compliance with ICH-GCP guidelines and regulatory requirements.

Clinical Trial Management

  • Support Global Trial Leads (GTLs) in managing global clinical studies.
  • Maintain study timelines, plans, and study-level documentation.
  • Ensure eTMF accuracy, completeness, and inspection readiness.
  • Update protocol milestones and country planning information in CTMS.
  • Support study startup, maintenance, and closeout activities.

Project Coordination

  • Facilitate study team meetings and document meeting minutes.
  • Monitor study performance metrics and quality indicators.
  • Identify operational risks and support mitigation strategies.
  • Coordinate cross-functional activities across global teams.

Vendor and Budget Management

  • Assist in vendor oversight activities.
  • Review vendor invoices and manage payment processing.
  • Track study accruals and support budget-related activities.
  • Manage vendor contracts, statements of work (SOW), and study payments.

Regulatory and Compliance Support

  • Support country-specific regulatory submissions and approvals.
  • Assist with IRB/IEC notifications and documentation.
  • Ensure adherence to SOPs, ICH-GCP guidelines, and company policies.

Study Closure Activities

  • Lead assigned archival and study closure activities.
  • Support Clinical Study Report (CSR) appendices when required.
  • Ensure proper documentation during trial closeout.

Required Qualifications

Education

  • Bachelor’s degree (BA/BS) in Life Sciences, Pharmacy, Biotechnology, Nursing, Clinical Research, or a related discipline preferred.

Experience

  • Minimum 2–4 years of experience in clinical research or clinical operations.
  • Experience with global clinical trials preferred.
  • Hands-on experience using:
    • Clinical Trial Management Systems (CTMS)
    • Electronic Trial Master File (eTMF) systems
    • Clinical research documentation platforms

Technical Skills

  • Knowledge of ICH-GCP guidelines.
  • Understanding of regulatory requirements and drug development processes.
  • Knowledge of clinical trial budgets and vendor management.
  • Project management exposure is advantageous.

Soft Skills

  • Strong communication and stakeholder management skills.
  • Ability to work in cross-functional global teams.
  • Problem-solving and risk management capabilities.
  • Ability to manage multiple priorities with minimal supervision.

Why Join Bristol Myers Squibb?

Bristol Myers Squibb is recognized globally for its innovation in biopharmaceutical research and development. Employees benefit from:

  • Exposure to global clinical trials.
  • Career growth opportunities across therapeutic areas.
  • Collaborative and inclusive work culture.
  • Competitive compensation and benefits.
  • Opportunities to contribute to life-changing medicines.
  • Learning and development programs.
  • Flexible work arrangements based on role requirements.

Location

Hyderabad, Telangana, India

This position operates under BMS’s hybrid/site-based work model depending on business requirements.

Salary Information

Based on current market benchmarks for Senior Global Trial Associate roles in Hyderabad:

Expected Salary Range: ₹8,00,000 – ₹14,00,000 per annum

Actual compensation may vary based on experience, skills, and internal compensation structures.

How to Apply

Application Link

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