Associate Jobs at BMS Life Sciences Jobs Global Trial Acceleration Associate
Global Trial Acceleration Associate role at BMS offering Associate Jobs in Life Sciences.
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Global Trial Acceleration Associate at BMS | Life Sciences Jobs | Apply Now

Looking to build a career through high-impact Associate Jobs? BMS offers exciting Life Sciences Jobs with its Global Trial Acceleration Associate role, where clinical operations, regulatory documentation, and global trial execution come together to support life-changing therapies worldwide.

  • Job Title: Global Trial Acceleration Associate
  • Job ID: R1593805
  • Location: Hyderabad

About the Company:

Bristol Myers Squibb (BMS) is a global biopharmaceutical leader committed to discovering, developing, and delivering innovative medicines that help patients overcome serious diseases. BMS fosters a culture of collaboration, balance, and continuous growth.

Job Overview:

The Global Trial Acceleration Associate job supports global clinical trials by managing centralized activities related to clinical documentation, regulatory submissions, site activation, and trial start-up. The role involves close collaboration with study teams, CROs, vendors, and internal stakeholders throughout the lifecycle of clinical studies.

Key Responsibilities:

  • Manage centralized clinical documentation for global trials
  • Support study start-up, maintenance, and close-out activities
  • Act as primary contact for document management and submissions
  • Coordinate with CROs, vendors, and internal study teams
  • Support site and country activation activities
  • Maintain and track essential trial documentation
  • Update clinical systems such as CTMS and eTMF
  • Ensure compliance with regulatory and ethical standards

Educational Requirements:

  • Minimum of Bachelor’s degree in Life Sciences or a related field. Advanced degree a plus.
  • Minimum 3 years of relevant clinical development & operational experience in Pharmaceutical, biotech, CRO or similar fields is required.

Skills Required:

  • Experience in clinical development or clinical operations
  • Knowledge of ICH-GCP and regulatory guidelines
  • Hands-on experience with regulatory documentation and submissions
  • Familiarity with CTMS, eTMF, and clinical trial systems
  • Strong organizational and time-management skills
  • Effective communication and stakeholder management abilities

These Associate Jobs at BMS offer a strong foundation for professionals seeking meaningful Life Sciences Jobs in global clinical research. Join Bristol Myers Squibb to accelerate clinical trials and contribute to therapies that truly transform lives.

APPLY HERE ONLINE

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