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PSG Global Solutions
San Francisco, CA, United States
Description We're looking for a Medical Writing Manager , working in Pharmaceuticals and Medical Products industry in 455 Mission Bay Boulevard, South San Francisco, California, 94158, United States . Job description: Writes and edits clinical reports, summarize data from clinical studies for submissions to the FDA and for publication and/or
Job Source: PSG Global SolutionsCorcept Therapeutics
Menlo Park, CA, United States
The Senior Manager, Medical Writing will collaborate with colleagues to write high-quality, strategically aligned medical-writing deliverables supporting the regulatory requirements of a clinical development program, ensuring completeness, accuracy, and compliance with US and ex-US regulatory requirements. Responsibilities: Author, co-author, cri
Job Source: Corcept TherapeuticsMeet Recruitment Limited
Menlo Park, CA, United States
Director, Medical and Regulatory Writing *Hybrid Role - Menlo Park, CA*' Meet has partnered with an exceptional Bay Area pharma focused in treatments for metabolic, psychiatric, and oncologic disorders. Our client has an approved product and a dynamic late-stage pipeline. They are looking for a Director of Medical/Regulatory Writing to join their t
Job Source: Meet Recruitment LimitedCorcept Therapeutics
Menlo Park, CA, United States
Corcept is leading the way in the research and development of cortisol modulators, molecules that regulate cortisol activity at the glucocorticoid receptor (GR). To date, we have discovered more than 1,000 selective proprietary cortisol modulators. In 2012, we received FDA approval of Korlym (mifepristone), the first approved treatment for hypercor
Job Source: Corcept TherapeuticsAnnexon
South San Francisco, CA, United States
Position Summary The Senior Director, Medical and Scientific Writing plays a critical role. Reporting to the SVP, Regulatory, Quality and Pharmacovigilance, you will work in partnership with a talented and collaborative team across our Research/Pre-Clinical, CMC, Regulatory, Clinical, and Quality organizations to author and drive development of key
Job Source: AnnexonMirum Pharmaceuticals
Foster City, CA, United States
Are you within a commutable distance to Foster City and willing to commit to a hybrid work schedule with being on site 2 days per week? * -- If you are not local to the Foster City area, are you willing to relocate? * Yes No I am local Are you currently authorized to work for any employer in the US without visa support? * -- By participating in
Job Source: Mirum PharmaceuticalsCytomX Therapeutics, Inc.
South San Francisco, CA, United States
Headquarters Location: South San Francisco, CA Candidate Location: Hybrid, Onsite or Remote Travel Required: 5% Reports To: Vice President, Clinical Development Department: Medical Writing Position Type: Full-time, Exempt About CytomX Therapeutics: CytomX Therapeutics, Inc. is committed to changing the
Job Source: CytomX Therapeutics, Inc.Annexon Biosciences
South San Francisco, CA, United States
Work Location Corporate Headquarters (South San Francisco, CA) – Hybrid Position Summary The Director / Senior Director, Medical and Scientific Writing plays a critical role. Reporting to the SVP, Regulatory, Quality and Pharmacovigilance, you will work in partnership with a talented and collaborative team across our Research/Pre-Clinical, CM
Job Source: Annexon BiosciencesSouth San Francisco, CA, United States
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The Opportunity
Description
We're looking for a Medical Writing Manager , working in Pharmaceuticals and Medical Products industry in 455 Mission Bay Boulevard, South San Francisco, California, 94158, United States .
Job description:
Writes and edits clinical reports, summarize data from clinical studies for submissions to the FDA and for publication and/or presentation.
Contributes to the development of formats medical writing infrastructure.
Remains informed of the latest professional, technological, and regulatory developments in medical writing, as well as therapeutic areas.
Supports all clinical writing activities outlined in the Project Clinical Development Plans (CDPs).
Our Client
Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success Bachelors/Masters degree in a scientific discipline with a strong journalism background is required (Equivalent experience may be accepted)
8 years in a pharmaceutical, biotech, or CRO medical writing position is required
6 years writing management experience is also required
Ability to create effective presentations from raw data is essential
Ability to interpret statistical and clinical data is a plus
Ability to work well with others in high-pressure situations
Must have demonstrated problem solving abilities
Strong organizational skills are required
Strong written and verbal communication skills are required
Understanding of clinical research, biostatistics, and regulatory affairs is required
Experience writing clinical protocols, clinical study reports, and IND sections
Good computer skills are required
Working knowledge of MS word, Excel, Power point, Project, and Outlook is a plus
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible?
Email Alert for Medical Writing Manager jobs in South San Francisco, CA, United States
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