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Bristol Myers Squibb is Hiring in Hyderabad | Apply Now for BMS Jobs

Ready to elevate your life science jobs journey with a global biopharmaceutical leader? Bristol Myers Squibb is hiring for BMS Jobs in Hyderabad, offering an impactful role as a Senior Global Trial Acceleration Associate. This opportunity is ideal for professionals seeking long-term growth within a prestigious Bristol Myers Squibb career in clinical operations and global trials.

Job Details

  • Job Details: Senior Global Trial Acceleration Associate
  • Location: Hyderabad – TS – IN

About the Company

Bristol Myers Squibb (BMS) is a global biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. With a strong focus on balance, flexibility, and professional growth, BMS provides employees with competitive benefits, career development programs, and opportunities to work on life-changing therapies across the globe.

Key Responsibilities

  • Manage centralized activities supporting global clinical trials
  • Act as main point of contact for clinical documentation and regulatory submissions
  • Coordinate with clinical sites, CROs, IRBs/IECs, and internal teams
  • Initiate and manage study start-up documentation and site activation activities
  • Maintain and review essential documents within eTMF and CTMS systems
  • Support ethical and regulatory submissions and approval tracking
  • Manage ongoing documentation updates, amendments, and correspondence
  • Ensure quality control of start-up and trial documentation
  • Support IRB/IEC processes including safety submissions and approvals
  • Assist with investigator site file preparation, IC adaptations, and CSR distribution

Educational Requirements

  • Bachelor’s degree in Life Science, or equivalent experience, Advanced degree preferred
  • 3–5 years of clinical development or operational experience in pharma, biotech, or CRO environments

Skills

  • Strong knowledge of ICH-GCP and regulatory guidelines
  • Experience with clinical trial documentation and start-up activities
  • Proficiency in CTMS, eTMF, and clinical trial systems (Veeva Vault preferred)
  • Excellent organizational, analytical, and time-management skills
  • Strong communication skills and stakeholder management ability
  • Ability to work effectively in cross-functional and global teams
  • High adaptability in fast-paced clinical research environments

If you are aiming to advance your life science jobs profile through globally impactful clinical trials, this role offers an exceptional platform. These BMS Jobs provide exposure to complex trial operations, regulatory coordination, and global stakeholders, making it a strong step forward in your Bristol Myers Squibb career.

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