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Medical Writing jobs

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INTERN - MEDICAL WRITING - REMOTE

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...

CompanyTeva Pharmaceuticals
AddressSylvania, PA
CategoryHealthcare
Date Posted just now See detail

Intern - Medical Writing - REMOTE New

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...

just now seen See more...

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...

4 days ago seen See more...

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...

a week ago seen See more...

Manager, Medical Writing

Pix11

New York, NY

The Medical Writer (Manager) creates documents pertaining to clinical studies and regulatory interactions, including (but not limited to) protocols, clinical study reports, briefing documents, clinical summaries for marketing appl...

2 weeks ago seen See more...

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...

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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...

2 weeks ago seen See more...

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...

2 weeks ago seen See more...

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...

2 weeks ago seen See more...

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...

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...

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...

Director- Medical Writing

Katalyst Healthcares & Life Sciences

Princeton, NJ

$177K - $225K a year

Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices. We have a few immediate job opportunities available in D...

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Senior Medical Writing Analyst (Remote)

Stryker Corporation

Sacramento, CA

$75,300 - $156,900 a year

Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations. Self-directed initiators. People who take ownership of their work...

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Section Head Medical Writing

Abbott

Des Plaines, IL

Career development with an international company where you can grow the career you dream of. . Free medical coverage for employees* via the Health Investment Plan (HIP) PPO. An excellent retirement savings plan with high employer...

a month ago seen See more...

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...

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...

Sr. Manager, Medical Writing - Delivery & Excellence

Moderna

Cambridge, MA

Vacation, sick time and holidays. Volunteer time to participate within your community. D iscretionary year-end shutdown. Paid sabbatical after 5 years; every 3 years thereafter....

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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