Medical Writer or Senior Medical Writer

When you work at St. Jude, you'll join a highly-collaborative work culture that inspires you every day to be your best. · ...

We're a team of researchers who decided to do medical communications differently. · ...

The Sr Medical Writer is responsible for providing clinical, scientific, and technical writing expertise for essential clinical, chemistry, manufacturing, and controls (CMC) documents submitted to the FDA and other regulatory agencies to support St. Jude's clinical development pi ...

When you work at St. Jude, you'll join a highly-collaborative work culture that inspires you every day to be your best. With opportunities for learning and growth, you can shape a career path that is right for you while also enjoying all the benefits and stability of working for ...

+A Medical Writer must be proficient in writing and editing technical scientific documents and managing content at all stages of development. · +Bachelor's Degree/Master's Degree equivalent in medical-related field or life science. · ...

The Medical Writer develops scientific and medical communication materials within BD Diagnostic Solutions (DS), collaborating with internal and external stakeholders to support evidence generation activities. · ...

The medical writer will oversee assigned medical writing projects including clinical study protocols reports INDs investigator brochures reviewing informed consent forms · Write edit manage production high-quality clinical documentation for submission to regulatory authorities ...

Medical Writer (Consultant) – Clinical Development / Early Feasibility Study · Contract-6-12+Months · Seattle, WA- Onsite · Immediate Need · Overview · We are seeking an experienced Medical Writer to support the initial drafting of a Clinical Development Plan and associated Ex-Vi ...

We are seeking a Medical Writer to support the Preclinical Engineering team with the creation, revision, and proofreading of technical reports and documentation related to bench and in vivo testing. · ...

· Company Description · Fishawack Group of Companies is a group of dynamic healthcare communications companies that includes US offices in the San Francisco and Philadelphia areas, as well as offices in the UK and Switzerland. Fishawack has a reputation built on excellence and c ...

This is a Medical Writer role that will be responsible for leading and executing all medical writing activities supporting Xeris' clinical programs.The individual will have a strong scientific background, exceptional writing skills, and the ability to translate complex clinical a ...

+ Develop scientific and medical communication materials within BD Diagnostic Solutions (DS), collaborating with internal and external stakeholders to support evidence generation and scientific exchange activities.+ As part of the MedComms team, the Medical Writer will focus on d ...

Marketing Healthcare Writer (part-time, romote) · Location: Morristown, NJ- Remote · Duration: Contract till January 2027 with possibility to extend · Shift: 1st, Monday to Friday · Note: · Shift: 1st Work Schedule: Mon-Fri, 9-5 est , 20-40hrs/week (depending on business needs) ...

HMP Global is an industry leader in providing CME activities for healthcare practitioners across a broad range of therapeutic areas. · ...

Our client is seeking a talented Medical Writer to join their growing international team. · ...

Job Title: Medical Writer - Medical Information (Payer & Health Systems) · Location: Titusville, NJ 08560 · 100% Onsite · Duration: 21 months contract · Work Hours: 8:00 AM – 4:30 PM · Position Summary · The Contractor Medical Writer, Medical Information – Payer & Health Systems ...

Work directly with clinical study teams in preparation of scientifically valid regulatory documents including protocols and protocol amendments. · ...

We are seeking a Medical Writer to support the Preclinical Engineering team with the creation, revision, and proofreading of technical reports and documentation related to bench and in vivo testing. · ...

The medical writer will be responsible for the management and oversight of assigned medical writing projects. · Write, edit and/or manage the production of high-quality clinical documentation including clinical study protocols. · Act as a member of clinical trial teams. · ...

The ideal candidate is a PhD-level scientific writer with demonstrated experience authoring peer-reviewed scientific publications. · They should have a strong scientific foundation and familiarity with the pharma R&D and clinical development lifecycle. · This individual must bala ...