Global Trial Acceleration Associate at Bristol Myers Squibb | Hyderabad
Global Trial Acceleration Associate at Bristol Myers Squibb | Hyderabad

Global Trial Acceleration Associate at Bristol Myers Squibb in Hyderabad

BMS careers offer a rare chance for professionals eager to make a difference in the biopharmaceutical field. The organization is seeking a Global Trial Acceleration Associate in Hyderabad, India, to support global clinical trials through effective documentation management, ethical submissions, and cross-functional coordination.

About Bristol Myers Squibb

Bristol Myers Squibb is a global biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. With a strong commitment to research and development, BMS operates in various therapeutic areas, including oncology, immunology, and cardiovascular diseases, striving to transform patients’ lives through science.

BMS Careers: Job Details

Company: Bristol Myers Squibb

Position: Global Trial Acceleration Associate

Location: Hyderabad, India

Job Description

In this BMS careers opportunity, the Global Trial Acceleration Associate will manage essential documentation and ensure compliance for global clinical trials. This role involves coordinating with various stakeholders, overseeing regulatory submissions, and maintaining clinical systems to support the execution of studies with precision.

Key Responsibilities

  • Manage and execute centralized activities for global clinical trials.
  • Coordinate with CROs, Country Trial Managers, Clinical Trial Monitors, and study teams.
  • Oversee essential document management and ethical/regulatory submissions.
  • Support outsourcing and contracting activities for global studies.
  • Conduct start-up documentation and site activation processes.
  • Review and maintain clinical systems (CTMS, eTMF, Veeva Vault).
  • Manage translation, investigator file setup, and document tracking.
  • Ensure quality control and compliance with ICH-GCP standards.
  • Act as the main point of contact for centralized start-up and maintenance activities.

Eligibility Criteria

  • Bachelor’s degree in Life Sciences, Legal, or Business Administration (Advanced degree preferred).
  • 3+ years of experience in clinical development or operations within pharma, biotech, or CROs.
  • Strong understanding of ICH-GCP and regulatory documentation processes.
  • Hands-on experience in IRB/IEC submissions, start-up documentation, and site activation.
  • Proficiency in MS Office, SharePoint, Veeva Vault, CTMS tools.
  • Excellent communication, organizational, and decision-making skills.
  • Prior therapeutic area experience (Oncology, Cardiology, Immunology) preferred.

Why Join Bristol Myers Squibb

Bristol Myers Squibb offers an opportunity to work that transforms patients’ lives through science. Employees benefit from competitive compensation, global career growth, and a collaborative, diverse, and inclusive work culture. The organization promotes a flexible hybrid work environment with on-site collaboration and provides wellness programs and continuous learning opportunities.

How to Apply

CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE

Conclusion

The opportunity at Bristol Myers Squibb for the role of Global Trial Acceleration Associate in Hyderabad is a significant one for qualified candidates exploring BMS careers in clinical research. Interested individuals are encouraged to apply before the deadline to seize this chance to contribute to impactful scientific advancements.

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