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Associate Director Medical Writing
RBW Consulting - CA, United States 1 days ago
This is a hybrid role with an onsite requirement of 3x per week.RBW is partnered with a mid-sized biotech company in their search for an ...
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Associate Director Medical Writing
RBW Consulting - Redwood City 7 hours ago
This is a hybrid role with an onsite requirement of 3x per week. RBW is partnered with a mid-sized biotech in p...
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Associate Director Medical Writing
RBW Consulting - San Mateo County, CA; California, US 2 hours ago
This is a hybrid role with an onsite requirement of 3x per week. RBW is partnered with a mid-sized biotech in part of their sear...
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Associate Director, Medical Writing
Rhythm Pharmaceuticals - Boston, Massachusetts, United States, 02298 2 days ago
Company Overview
Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of people living with rare neuroen...
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Associate Director Medical Writing
RBW Consulting - Redwood City 1 days ago
This is a hybrid role with an onsite requirement of 3x per week. RBW is partnered with a mid-sized biotech in part of their search fo...
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Associate Director/Director, Medical Writing
Calico LLC - San Francisco, CA, US, 94199 3 days ago
We’re explorers, optimists, scientists, engineers, inventors, technologists, drug developers and more, working together to make a difference in peo...
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Associate Director, Clinical Medical Writing
BIOMARIN - MS, United States 2 days ago
Who We Are BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new me...
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Go to next pageRBW Consulting - CA, United States
This is a hybrid role with an onsite requirement of 3x per week.
RBW is partnered with a mid-sized biotech company in their search for an Associate Director of Medical Writing to focus on Regulatory documents and interactions. In this role, you will be responsible for developing and executing strategies and documents for regulatory authority submissions. This position reports to the Head of Regulatory Affairs.
Qualifications:
- Extensive Regulatory Medical Writing experience in the pharmaceutical industry
- Experience with submissions to the FDA (IND / NDA) and EMA
- Proven track record in writing, editing, formatting, and finalizing regulatory documents, including updates to regulatory submissions, briefing books, annual reports, and DSURs
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Associate Director Medical Writing
