Writer creating and updating System Operations procedures for Eversource's electric system operations. Ensuring compliance with standards and coordinating with various departments.
About the role
- Associate Director leading medical writing for oncology at Johnson & Johnson. Responsible for regulatory submissions and process improvements with a focus on patient care.
Responsibilities
- Able to function as a lead writer on any compound independently
- Contributes to and champions internal standards, regulatory, and publishing guidelines
- Guides or trains cross-functional team members on processes and best practices
- Proactively identifies and champions departmental process improvements
Requirements
- Minimum of a Bachelor's Degree is required
- 10 years of relevant pharmaceutical/scientific experience
- 8 years of relevant clinical/regulatory medical writing experience
- 2 years of people management experience
- Advanced knowledge of regulatory guidance documents such as ICH requirements
- Excellent oral and written communication skills
- Strong leadership skills
Benefits
- Inclusive work environment
- Commitment to diversity and dignity
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
Associate Director leading regulatory medical writing teams for oncology at Johnson & Johnson. Overseeing project strategies and managing internal teams in a medical writing capacity.
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