Full-Time Medical Write jobs
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DIRECTOR, REGULATORY AND MEDICAL WRITING
Prepare and finalize clinical and/or regulatory documents such as, but not limited to, nonclinical and clinical study protocols, protocol amendments, Investigator's Brochures, regulatory briefing documents, health authority respon...
| Company | Biospace |
|---|---|
| Address | Remote - South San Francisco, CA |
| Category | Healthcare |
| Job type | Full time |
| Date Posted | 4 hours ago See detail |
Director, Regulatory and Medical Writing New
Biospace
Remote - South San Francisco, CA
Prepare and finalize clinical and/or regulatory documents such as, but not limited to, nonclinical and clinical study protocols, protocol amendments, Investigator's Brochures, regulatory briefing documents, health authority respon...
4 hours ago seen See more...
- View all - jobs in South San Francisco, CA
Associate Director, Medical Writing New
Biospace
Boston, MA
Author and manage clinical regulatory documents, such as Clinical Protocols (Phase 1-3 and specialty clinical pharmacology protocols), Protocol Amendments, Clinical Study Reports (CSR), narratives, Clinical and Safety Summaries, D...
10 hours ago seen See more...
- View all - jobs in Boston, MA
Intern - Medical Writing - REMOTE
Teva Pharmaceuticals
Sylvania, PA
Direct involvement in the daily business and gain in-depth insight into the Global Regulatory Medical Writing department. Supported by a mentor and experienced colleagues, actively assist in the planning and preparation of clinica...
3 days ago seen See more...
- View all - jobs in Sylvania, PA
Associate Director - Medical Writing
Biospace
Princeton, NJ
Provides strategic input into documents and plans to support clinical operations and regulatory submissions across a range of development programs and therapeutic areas:. Uses professional experience to provide advanced input into...
7 days ago seen See more...
- View all Biospace jobs - jobs in Princeton, NJ
ASSOCIATE DIRECTOR/DIRECTOR OF MEDICAL WRITING
Capricor Inc
Olin, NC
Bachelors degree (B.A. /B.S.) in scientific or medical field 10+ years of experience in medical/technical writing in the Biotech/Pharmaceutical industry Experience in the preparation of clinical/preclinical sections and/or docume...
2 weeks ago seen See more...
- View all Capricor Inc jobs - jobs in Olin, NC
Associate Director, Medical Writing
Biospace
Cambridge, MA
Functional Knowledge: Possess specialized depth and breadth of knowledge for managing Medical Writing and regulatory writing within a clinical development program.. Document Planning and Project Management: Coordinate and oversee...
2 weeks ago seen See more...
- View all Biospace jobs - jobs in Cambridge, MA
Associate Director Medical Writing
Biospace
Remote - Indiana, United States
In collaboration with clinical and regulatory, manages the authoring and document life cycle of clinical protocols and amendments, clinical study reports (CSRs), Investigators Brochures (IBs), electronic Common Technical Document...
3 weeks ago seen See more...
- View all Biospace jobs - jobs in Indiana State
Senior Manager, Medical Writing
Biospace
Cambridge, MA
Functional Knowledge: Apply an in-depth conceptual and practical knowledge of concepts, theories, and principles of Medical Writing and regulatory writing within a clinical development program.. Document Planning: Develop and mana...
3 weeks ago seen See more...
- View all Biospace jobs - jobs in Cambridge, MA
Director / Senior Director, Medical Writing
Biospace
South San Francisco, CA
Lead and direct all aspects of critical writing activities within Annexon, working cross-functionally to develop and produce high-quality deliverables such as clinical study protocols, IBs, CSRs, INDs/CTDs/amendments, analysis and...
3 weeks ago seen See more...
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Director, Medical Writing Delivery and Excellence
Biospace
Cambridge, MA
Functional Knowledge: Demonstrate a comprehensive understanding of concepts and principles for overseeing the managing Medical Writing and regulatory writing across multiple clinical development programs.. Document Planning & Proj...
4 weeks ago seen See more...
- View all Biospace jobs - jobs in Cambridge, MA
Associate Director Medical Writing
Lilly
Indianapolis, IN
BS and at least 5 years of related experience (advanced degree (e.g., MS/PhD/PharmD) may compensate for years of experience) Prior medical technical writing experience within the biotech/pharmaceutical/clinical research organizati...
4 weeks ago seen See more...
- View all Lilly jobs - jobs in Indianapolis, IN
Medical Writing Projects Director
Scholar Rock
Remote
$133K - $168K a year
Create, supervise, and direct complicated document submission plans and teams for marketing applications. Collaborate with cross-functional partners to drive development, review, and finalization timelines for submission documents...
a month ago seen See more...
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Associate Director, Medical Writing
Avidity Biosciences
San Diego, CA
$176,600 - $195,200 a year
Ensure documents are planned, developed, managed, reviewed, quality checked, and approved according to mutually agreed timelines with input from all critical stakeholders in accordance with Avidity Regulatory Affairs and Developme...
2 months ago seen See more...
- View all Avidity Biosciences jobs - jobs in San Diego, CA
Executive Director, Data Science & Medical Writing
Mitsubishi Tanabe Pharma
Jersey City, NJ
Acts as global lead for the development and execution of biostatistics, statistical programming, and data management strategies to support clinical development activities. Oversees statistical leadership into the ongoing clinical...
2 months ago seen See more...
Senior Director, Medical Writing
Cytomx Therapeutics, Inc.
South San Francisco, CA
Supervise the preparation of all key documents related to the conduct and reporting of clinical studies at CytomX. These include, but are not limited to, regulatory submissions (e.g., protocols, informed consent forms, Investigato...
2 months ago seen See more...
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