Bristol-Myers Squibb (BMS) Hiring Document Coordinator, Global Trial Acceleration

Document Coordinator, Global Trial Acceleration – Join  Life-Changing Team in Hyderabad

Join Bristol Myers Squibb (BMS), a pioneer in the biopharmaceutical industry, where every role is an opportunity to make a significant impact. We seek a dedicated Document Coordinator to contribute to our mission of transforming patients through science. This is not just a job; it’s a chance to be part of something bigger and to grow with a company that values balance, flexibility, and the personal goals of its employees. Learn more about our culture at careers.bms.com/working-with-us.

Position Summary

As a Document Coordinator, you will be pivotal in supporting BMS Clinical Trials globally. Your expertise will be crucial in creating and managing Clinical Trial Application (CTA) packages and ensuring seamless collaboration with clinical trial vendors. This is a unique opportunity to work in a dynamic environment that offers growth and the chance to be part of a diverse, high-achieving team.

Key Responsibilities

• Manage centralized activities supporting global trials with a focus on clinical documentation.
• Engage with clinical study sites, IRBs/IECs, CROs/vendors, and internal BMS teams to support studies from start-up to close-out.
• Serve as the main point of contact for document management, ethical, and regulatory submission-related activities.
• Initiate and manage start-up documentation activities, ensuring compliance with regulatory standards and BMS policies.
• Act as a central point of contact during study start-up and provide ongoing support and communication with sites and study teams.

Qualifications & Experience

• Bachelor’s in legal, life science, business administration, or equivalent experience; an advanced degree is a plus.
• 1-2 years of relevant experience in the pharmaceutical, biotech, CRO, or related fields.
• Proficiency in ICH/GCP, regulatory guidelines, and clinical trial processes.
• Strong organizational, analytical, and decision-making skills.
• Excellent communication skills in English and proficiency in MS Office, SharePoint, and CTMS (Veeva Vault experience preferred).

Apply online

Why Join Us

At BMS, you will find a challenging, meaningful, and life-changing career. We empower our employees to leverage their talents and perspectives in an inclusive culture that values diversity in clinical trials. Our shared values of passion, innovation, urgency, accountability, inclusion, and integrity bring out the best in our colleagues.

Application Process

If you’re intrigued by the prospect of contributing to work that goes beyond the ordinary, we encourage you to apply, even if your resume doesn’t perfectly match the role. You could be just one step away from a transformative career move.

Tagged as: API Manufacturing, Good Clinical Practice (GCP), Pharmaceutical Careers, Pharmaceutical Jobs