Proclinical Staffing
Director, Medical Writing
Proclinical Staffing, San Francisco, California, United States, 94199
Overview
Medical Writing Positions in San Francisco - Relo Package Available Company & Location
Company: A leading commercial biotech in the San Francisco Bay Area Location: San Francisco Bay Area (Hybrid: 3 days on-site) Relocation: A comprehensive relocation package is available for candidates. Responsibilities
Create, edit, and manage regulatory documents. Contribute to the overall regulatory strategy. Support multiple positions at the Director, Associate Director, and Senior Manager levels. Qualifications
Experience in regulatory medical writing within the biotech or pharmaceutical industry. Demonstrated expertise in authoring regulatory submissions (e.g., NDAs, INDs, etc.). Strong understanding of regulatory guidelines (e.g., FDA, EMA, ICH). Exceptional communication and collaboration skills. Compensation & Benefits
Market-beating base salary and a competitive bonus structure. Significant stock equity. 100% company-paid medical, dental, and vision coverage for employees. Generous Paid Time Off (PTO) and retirement plan. Compensation: $220,000.00 - $250,000.00 Per Annum How to Apply
If you are having difficulty applying or if you have any questions, please contact
George Watson
at
g.watson@proclinical.com . If you are interested in applying to this exciting opportunity, please click 'Apply' or, to speak to one of our specialists, request a callback at the top of this page. About Proclinical
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you have read and understood our privacy policy, which informs you how we process and safeguard your data.
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Medical Writing Positions in San Francisco - Relo Package Available Company & Location
Company: A leading commercial biotech in the San Francisco Bay Area Location: San Francisco Bay Area (Hybrid: 3 days on-site) Relocation: A comprehensive relocation package is available for candidates. Responsibilities
Create, edit, and manage regulatory documents. Contribute to the overall regulatory strategy. Support multiple positions at the Director, Associate Director, and Senior Manager levels. Qualifications
Experience in regulatory medical writing within the biotech or pharmaceutical industry. Demonstrated expertise in authoring regulatory submissions (e.g., NDAs, INDs, etc.). Strong understanding of regulatory guidelines (e.g., FDA, EMA, ICH). Exceptional communication and collaboration skills. Compensation & Benefits
Market-beating base salary and a competitive bonus structure. Significant stock equity. 100% company-paid medical, dental, and vision coverage for employees. Generous Paid Time Off (PTO) and retirement plan. Compensation: $220,000.00 - $250,000.00 Per Annum How to Apply
If you are having difficulty applying or if you have any questions, please contact
George Watson
at
g.watson@proclinical.com . If you are interested in applying to this exciting opportunity, please click 'Apply' or, to speak to one of our specialists, request a callback at the top of this page. About Proclinical
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you have read and understood our privacy policy, which informs you how we process and safeguard your data.
#J-18808-Ljbffr