Scientific Document Coordinator
1 month ago
Transforming Lives through Innovative Science
Bristol Myers Squibb is a global biopharmaceutical company that is committed to transforming lives through innovative science. We are seeking a highly skilled Scientific Document Coordinator to join our team in Hyderabad.
Key Responsibilities
- Coordinate and author complex documents needed for regulatory submissions, ensuring the coordination and integration of scientific, medical, and regulatory input from cross-functional team members.
- Participate in relevant document subteams and ensure effective planning and management of timelines for all components of assigned documents.
- Participate in document strategy sessions, including messaging, document flow, logic, and consistency for assigned projects.
- Review and edit documents as required.
- Serve as a liaison for external documentation support and prepare specifications for the work.
Qualifications & Experience
- PharmD/PhD in a relevant scientific discipline or Master's/Bachelor's degree with approximately 5 years of pharmaceutical regulatory documentation experience.
- Demonstrated strong writing skills in authoring and managing the production of complex clinical documents.
- Good understanding of global pharmaceutical drug development and requirements for documentation authoring supporting regulatory submissions.
- Demonstrated ability to manage timelines and quality of work using strong organizational, communication, facilitation, and interpersonal skills in a cross-functional team.
About Bristol Myers Squibb
Bristol Myers Squibb is a global biopharmaceutical company that is committed to transforming lives through innovative science. We are a leader in the development and delivery of innovative medicines and vaccines for serious diseases.
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