BMS Life Science Document Coordinator Job, Apply Now
Welcome to Bristol Myers Squibb, a global biopharmaceutical company dedicated to bringing life-transforming medicines to patients worldwide. We are seeking a meticulous and organized Document Coordinator to join our Global Trial Acceleration team in Hyderabad, India. If you hold a Bachelor’s degree in life sciences or a related field and are passionate about supporting global clinical trial operations through efficient document management, we encourage you to apply!
Welcome to Bristol Myers Squibb
Bristol Myers Squibb is a global biopharmaceutical company committed to bringing transformative medicines to patients around the world. We aim to discover, develop, and deliver innovative therapies that help address some of the most challenging diseases of our time.
Job Title: Document Coordinator, Global Trial Acceleration (Global Trial Acceleration Associate)
We are seeking a Document Coordinator to join our Global Trial Acceleration team in Hyderabad, India. As a key member of our team, you will play a crucial role in ensuring the efficient management of trial-related documents to support our global clinical trial operations.
Key Responsibilities:
As a Document Coordinator, your responsibilities will include:
- Coordinating the efficient collection, thorough review, and secure archival of essential trial-related documents.
- Ensuring strict compliance with all relevant regulatory requirements and internal quality standards for document management.
- Providing comprehensive support to study teams in all aspects of document management activities throughout the clinical trial lifecycle.
- Collaborating effectively with cross-functional teams to streamline existing document management processes and drive improvements in overall efficiency.
Qualifications:
To be successful in this role, you should possess the following qualifications:
- A Bachelor’s degree in life sciences or a closely related scientific field.
- Prior experience in clinical research operations or document management within a clinical trial setting is preferred.
- Strong attention to detail with exceptional organizational and time management skills.
- Excellent written and verbal communication skills, enabling clear and effective interaction with team members and stakeholders.
If you are passionate about making a tangible difference in the lives of patients and thrive in a dynamic and collaborative work environment, we encourage you to apply for this exciting opportunity to join our Global Trial Acceleration team in Hyderabad.
Keywords: document coordinator, global trial acceleration, clinical trials, document management, Bristol Myers Squibb, Hyderabad, India. BMS Life Science Document Coordinator Job, Apply Now
