Bristol Myers Squibb Hiring Scientific Writer

At Bristol Myers Squibb, we value work that is demanding, fulfilling, and transformative. Our mission is to use science to improve the lives of patients. Our work affects patients all around the world and varies from improving production processes to making significant advancements in cell treatment. We provide a broad and welcoming work environment with unusually large and comprehensive growth and development opportunities.

Position: Scientific Writer II

Location: Hyderabad, Telangana, India

Position Summary: As a Scientific Writer II, you will coordinate and author documents required for regulatory submissions, ensuring integration of scientific, medical, and regulatory input from cross-functional team members.

Key Responsibilities:

Coordinate and author regulatory documents (e.g., Investigator’s Brochures, development safety update reports, clinical study reports) with input from development team members.
Participate in document subteams, planning, and managing timelines for assigned documents.
Participate in document strategy sessions, ensuring messaging, flow, logic, and consistency.
Maintain document prototypes and shells.
Comply with internal and external processes and guidelines, managing the review process to ensure timely completion and high quality.
Review and edit documents as required.

Qualifications & Experience:

PharmD/PhD in a relevant scientific discipline or Master’s/Bachelor’s degree with 2-4 years of regulatory documentation experience.
Strong writing skills in authoring IB, Safety Aggregate Report, Clinical Protocols, and/or CSR.
Ability to analyze and interpret complex data from various scientific disciplines.
Understanding of global pharmaceutical drug development.
Demonstrated ability to manage timelines and quality of work in a cross-functional team.
Working knowledge of a document management system and document publishing process
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