Bristol Myers Squibb Hiring Document Coordinator

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About Bristol Myers Squibb:
Bristol Myers Squibb seeks a Senior Document Coordinator for the GTAC team, focusing on global trial and alliance coordination.

Position: Senior Document Coordinator (GTAC)

Organization: Bristol Myers Squibb

Qualifications:

  • B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Life Sciences

Experience: 3 to 7 years in relevant industry roles

Salary: Not disclosed

Location: Hyderabad (Hybrid model, 2-3 days onsite per week)

Key Responsibilities:

  1. Global Site Initiation: Manage and coordinate global site initiation documentation.
  2. Study Start-Up Documentation: Prepare protocols and ICFs for global study start-up.
  3. NDA/CDA and CTA Dossiers: Handle NDA, CDA, and CTA dossier preparation.
  4. Clinical Trial Management System (CTMS): Ensure compliance and accuracy in CTMS data.

Required Skills:

  • Extensive experience in global site initiation and study start-up documentation.
  • Proficiency in preparing protocols, ICFs, NDA/CDA, and CTA dossiers.
  • Familiarity with Clinical Trial Management Systems.
  • Strong organizational and communication skills.

How to Apply:
Send your updated resume to pooja.bombrade@iqvia.com if interested.


Meta Description (19 words):
Bristol Myers Squibb is hiring a Senior Document Coordinator in Hyderabad for global trial and alliance coordination. Apply now!

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