Scientific Document Coordinator

1 month ago


Hyderabad, Telangana, India Bristol Myers Squibb Full time

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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