- University of Miami (Miami, FL)
- …SCCC - Protocol Development Office (PDO) has an exciting opportunity for a Full Time Scientific Writer (Medical Writer ) to work Remotely. CORE JOB SUMMARY ... The Scientific Writer analyzes scientific ...of clinical trials including protocol and ICF development, institutional regulatory submissions (Protocol Review and Monitoring Committee [PRMC] and… more
- Houston Methodist (Houston, TX)
- The Scientific Writer at Houston Methodist, Department of Digital Health Innovation and Implementation Research position must have experience writing and editing ... science publications, and working with vendor and industry partners and executives. The scientific writer should have experience sourcing ways to present story… more
- Houston Methodist (Houston, TX)
- At Houston Methodist, the Senior Scientific Writer contributes to faculty success by collaborating with scientific and clinical teams to coordinate, develop, ... study protocols, executive summaries, and strategic and progress reports. The Senior Scientific Writer also provides project management, mentors junior staff and… more
- ThermoFisher Scientific (Greenville, NC)
- …Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** At Thermo Fisher Scientific , you will discover meaningful work that makes a positive ... are seeking an experienced and highly skilled Principal Medical Writer to join our team. The Principal Medical ...reviewing, and managing a wide range of clinical and regulatory documents. This role requires a strong understanding of… more
- University of Miami (Miami, FL)
- …experimental) for comprehensive analysis, assisting in the preparation of scientific manuscripts, presentations, and regulatory submissions. This list ... application templates for grant proposals. Formats substantive copy and scientific editing, proofreading, and finalizing documents as required and requested.… more
- System One (Park Ridge, NJ)
- Title: Sr Regulatory Writer - R&D Location: Park Ridge, NJ area Schedule: M-F Full Time Type: Direct Hire Responsibilities: Our client is seeking Regulatory ... scientific documents for accuracy, formatting, consistency, and compliance with scientific principles, regulatory guidelines, company standards, and industry… more
- AbbVie (Irvine, CA)
- …that support the company's objectives. Responsibilities The Principal Strategic Medical Writer independently writes most clinical and regulatory documents within ... Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Principal Strategic Medical Writer is responsible for leading and writing clinical and regulatory… more
- ICON Clinical Research (New York, NY)
- …pivotal role in the development and preparation of clinical trial documents, regulatory submissions, and scientific publications, contributing to the advancement ... Medical Writer II- Farmingdale, NY- Hybrid ICON plc is...format, and presentation. + Keeping abreast of emerging trends, scientific developments, and regulatory updates in relevant… more
- System One (New Haven, CT)
- …in the preparation of FDA IND Module 2 content, ensuring alignment with regulatory standards. + Translate complex scientific data into clear, user-friendly ... Job Title: Medical Writer (part time) Location: Northeast (EST) candidates preferred...(Module 2). The role ensures document quality, consistency, and regulatory compliance while collaborating closely with internal and external… more
- Terumo Neuro (Aliso Viejo, CA)
- … scientific experience. 3. Demonstrated experience in the development of regulatory / clinical submissions (preferably as a medical writer for pharmaceutical, ... **12640BR** **Title:** Sr. Medical Writer **Job Description:** **INNOVATION STARTS WITH YOU** Are...job duties include: + Collaborating with the clinical & regulatory teams to write clinical documents for regulatory… more