Scientific Writer II
3 weeks ago
Transformative Work at Bristol Myers Squibb
At Bristol Myers Squibb, we're pushing the boundaries of what's possible in the pharmaceutical industry. Our work is focused on helping patients prevail over serious diseases by building sustainable and innovative solutions. As a Scientific Writer II, you'll play a critical role in this mission by coordinating and authoring documents needed for regulatory submissions.
Key Responsibilities
- Coordinate and author regulatory documents, 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.
- Maintain document prototypes and shells, and comply with internal and external processes and guidelines.
- Review and edit documents as required.
Qualifications & Experience
- PharmD/PhD in a relevant scientific discipline or Master's/Bachelor's degree with approximately 2-4 years of regulatory documentation experience.
- Demonstrated strong writing skills in authoring and managing the production of regulatory documents.
- Ability to analyze and interpret complex data from a broad range of scientific disciplines.
- Understanding of global pharmaceutical drug development.
- Demonstrated ability to manage timelines and quality of work using strong organizational, communication, facilitation, and interpersonal skills in a cross-functional team.
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