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Bristol Myers Squibb Hiring Global Trial Acceleration Associate

Bristol Myers Squibb Hiring Global Trial Acceleration Associate

Position: Global Trial Acceleration Associate
Organization: Bristol Myers Squibb (BMS)
Qualification: Bachelor’s Degree in Life Sciences, Legal, or Business Administration (Advanced degree preferred)
Location: Hyderabad, India
Experience: Minimum 3 Years
Job Type: Full-Time
Application Mode: Online
Verified Job


Bristol Myers Squibb Global Trial Acceleration Associate Jobs in Hyderabad

Bristol Myers Squibb (BMS), one of the world’s leading biopharmaceutical companies, is inviting experienced professionals to apply for the position of Global Trial Acceleration Associate based in Hyderabad, India. This position plays a crucial role in supporting global clinical trial operations, documentation management, and coordination across international study teams. Bristol Myers Squibb Hiring Global Trial Acceleration Associate

At BMS, employees are united by a shared mission — transforming patients’ lives through science. The company is committed to fostering innovation, collaboration, and excellence across all areas of drug discovery and clinical development. If you are passionate about making a meaningful impact in healthcare, this opportunity offers a platform to grow your career in global clinical research operations. Bristol Myers Squibb Hiring Global Trial Acceleration Associate


Job Description – Global Trial Acceleration Associate

The Global Trial Acceleration Associate will be responsible for managing essential documentation, regulatory submissions, and operational coordination for global clinical studies. This role ensures that studies are initiated, executed, and maintained in compliance with regulatory and ethical standards, supporting BMS’s mission to deliver life-changing therapies worldwide. Bristol Myers Squibb Hiring Global Trial Acceleration Associate

Key Responsibilities:

  • Manage and execute centralized operational activities for global clinical trials.
  • Coordinate with Country Trial Managers, Clinical Trial Monitors, CROs, and other cross-functional study teams.
  • Oversee ethical and regulatory submissions, ensuring all documents are accurate and compliant.
  • Support outsourcing, contracting, and vendor management activities for clinical studies.
  • Manage start-up documentation and assist in site activation procedures.
  • Maintain and update clinical systems, including CTMS, eTMF, and Veeva Vault.
  • Coordinate translation, investigator file setup, and document tracking across study sites.
  • Ensure quality control and adherence to ICH-GCP guidelines throughout all trial phases.
  • Act as the primary point of contact for centralized start-up and maintenance processes.
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Qualifications and Experience

Educational Qualification:

  • Bachelor’s Degree in Life Sciences, Legal, or Business Administration (Advanced degree preferred).

Professional Experience:

  • Minimum of 3 years of experience in clinical research, development, or operations within a pharmaceutical, biotechnology, or CRO environment.
  • Strong understanding of ICH-GCP guidelines and global regulatory documentation processes.
  • Proven experience in IRB/IEC submissions, start-up documentation, and site activation.
  • Proficiency in clinical trial systems such as CTMS, eTMF, and Veeva Vault.
  • Solid knowledge of MS Office and SharePoint.

Skills and Competencies:

  • Excellent communication and organizational skills.
  • Strong attention to detail and ability to handle multiple priorities effectively.
  • Sound decision-making and problem-solving abilities.
  • Prior experience in therapeutic areas like Oncology, Cardiology, or Immunology is an added advantage.
  • Bristol Myers Squibb Hiring Global Trial Acceleration Associate

Why Join Bristol Myers Squibb?

  • Work that directly contributes to improving and transforming patients’ lives.
  • Competitive compensation and benefits packages.
  • Opportunity for global career advancement within a world-class biopharma organization.
  • Inclusive, diverse, and collaborative workplace culture.
  • Flexible hybrid work model that supports both on-site and remote collaboration.
  • Access to wellness initiatives and professional development programs.
  • Bristol Myers Squibb Hiring Global Trial Acceleration Associate

Job Details

  • Position: Global Trial Acceleration Associate
  • Department: Global Clinical Operations
  • Company: Bristol Myers Squibb (BMS)
  • Location: Hyderabad, India
  • Experience: Minimum 3 Years
  • Employment Type: Full-Time
  • Posted On: October 12, 2025

How to Apply

Interested and eligible candidates can apply through the official Bristol Myers Squibb careers portal. Bristol Myers Squibb Hiring Global Trial Acceleration Associate

Application Link


About Bristol Myers Squibb

Bristol Myers Squibb is a global biopharmaceutical leader focused on discovering, developing, and delivering innovative medicines that help patients overcome serious diseases. With a strong portfolio spanning oncology, immunology, cardiovascular, and fibrosis, BMS combines cutting-edge science with a deep commitment to patient outcomes. Bristol Myers Squibb Hiring Global Trial Acceleration Associate

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The company’s culture is driven by integrity, inclusion, and a shared purpose — transforming lives through science. By joining Bristol Myers Squibb, you will be part of a global team that values collaboration, excellence, and a relentless pursuit of innovation. Bristol Myers Squibb Hiring Global Trial Acceleration Associate

For verified pharma job updates, visit PharmaJobHub.in India’s trusted pharma career portal.

Note: This job information is sourced from publicly available official sources. We share it for reference purposes only and do not claim ownership of the job posting.


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