Job Summary

The GDO Submission Document Manager leads the development and delivery of clinical and regulatory submission documentation supporting global health authority submissions. This role coordinates cross-functional stakeholders, drives submission readiness, manages risks and timelines, and ensures high-quality, compliant deliverables for regulatory filings. The position combines regulatory operations expertise, project leadership, and strategic problem-solving to support successful drug development programs.

Responsibilities
Lead the development and delivery of clinical and regulatory submission documentation supporting global health authority submissions.
Coordinate cross-functional stakeholders.
Drive submission readiness.




Manage risks and timelines.
Ensure high-quality, compliant deliverables for regulatory filings.

Skills
Regulatory submissions
Regulatory operations
Project leadership
Stakeholder coordination
Risk management
Timeline management
Regulatory filings
Drug development

Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

📌 Gdo Submission Document Manager Hyderabad
🏢 Bristol-Myers Squibb
📍 Hyderabad