Senior Medical Writing Manager
6 days ago
BioMarin Pharmaceutical Inc. offers an exciting opportunity for an experienced Senior Medical Writing Manager to join our team, responsible for leading the development and review of regulatory documents and managing project teams.
About the RoleThe successful candidate will have at least 10 years of experience as a medical writer in the pharmaceutical industry, with a minimum of 3 years administrative and/or functional management experience. They will be responsible for planning and managing development of regulatory documents, as well as overseeing project teams and resource allocation.
Key Responsibilities:
- Develop and review regulatory documents, including submissions and publications.
- Collaborate with the Head of Clinical Medical Writing to plan and manage departmental resources, timelines, and budget.
- Manage vendor relationships for outsourced projects and oversee the development of standard processes and templates.
- Coach and mentor medical writers, promoting career development within the team.
Requirements:
- At least 10 years of experience as a medical writer in the pharmaceutical industry.
- Minimum of 3 years administrative and/or functional management experience.
- Proven track record in budgeting documentation projects and experience with delegating and overseeing projects and tasks.
- Computer/Office Equipment Skills: Proficiency in Microsoft Word, Excel, Adobe Acrobat, and PowerPoint.
- Experience using document management software and regulatory knowledge, including ability to plan and manage development of regulatory documents.
Estimated Salary: $155,000 - $190,000 per year
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