Principal Medical Writer
Employment type
Full-time
Work setting
On-site
Location
Emeryville, CA
Schedule
Day shift
Posted
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Job overview
The Principal Medical Writer is an onsite role based in Emeryville, CA. Compensation is not specified for this regulatory writing position, which supports the development of clinical and regulatory documents for the BeOne pipeline. This role provides expertise in creating high-quality clinical study protocols, reports, and regulatory submissions. It involves mentoring junior writers and leading document strategy to facilitate the development, submission, and approval of products.
What you'll do
- Manages writing tasks for clinical and regulatory documents.
- Leads document strategy and development in collaboration with study teams.
- Mentors junior writers and contributes to process optimization.
- Ensures adherence to regulatory guidelines and SOPs.
What we're looking for
- Skills & competencies
- full-timeday shiftemeryville cabeone medicinesmedical writingregulatory affairsclinical documentationbiotechmentorshiponsite
- Work arrangement
- Weekend coverage required
Why this role
Focuses on complex regulatory document writing and mentoring within a global medical writing scope.
About the employer
BeOne Medicines is hiring for this role. Industry: Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology). Sector: 54.
Additional details
- Industry sector
- 54
- Industry
- Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)
- Occupation code
- 11-9121.01
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Listing ID: 9bc850cc-9a18-40e6-ab40-bed5e569cdfc