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:
- Global Site Initiation: Manage and coordinate global site initiation documentation.
- Study Start-Up Documentation: Prepare protocols and ICFs for global study start-up.
- NDA/CDA and CTA Dossiers: Handle NDA, CDA, and CTA dossier preparation.
- 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!