- 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
- 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
- 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
- State of Colorado (Denver, CO)
- …Protection Intern - Water Quality Permit Writer - 2461 Print (https://www.governmentjobs.com/careers/colorado/jobs/newprint/4873290) Apply Environmental ... Protection Intern - Water Quality Permit Writer - 2461 Salary $4,872.00 - $5,845.00 Monthly Location...groundwater. Additional core work assigned to the unit includes regulatory development and issuance of reuse notices of authorization… more
- AbbVie (San Francisco, CA)
- …LinkedIn. Allergan Aesthetics | An AbbVie Company Job Description Purpose The medical writer is responsible for providing clinical regulatory document support to ... US and international regulations, requirements and guidance associated with scientific publications or clinical regulatory document preparation Qualifications… more
- Actalent (San Francisco, CA)
- Job Title: Principal Medical Writer IIJob Description The Associate Director, Principal Medical Writer II is responsible for developing clinical documents for ... submissions to regulatory authorities globally. You will provide strategic direction to...activities of multiple compounds and serve as the lead writer for individual summary documents. You will have a… more
- Publicis Groupe (Philadelphia, PA)
- …5 of the top 8 pharma companies on our roster. **Overview** This dedicated writer will be responsible for the conception and execution of innovative print and ... be exactly who we are looking for. **ABOUT THE SCIENTIFIC TEAM** Here at the Medical team, we are...influence goes beyond the agency too-clients, stakeholders, and the Medical/Legal/ Regulatory review (MLR) team look to us for insights… more
- BeOne Medicines (Emeryville, CA)
- …Required: + At a minimum 4 years' relevant industry experience as a regulatory medical writer with a BA/BS degree; PhD/PharmD in life sciences ... **General Description:** The Senior Medical Writer is responsible for writing, editing, and formatting... is responsible for writing, editing, and formatting clinical regulatory documents that conform to domestic and/or international … more
- Kelly Services (Sunnyvale, CA)
- Kelly(R) Science & Clinical is seeking a Technical Writer for a 6-month contract opportunity with a leading molecular diagnostics company at their headquarters in ... Sunnyvale, CA. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career,… more
- Kelly Services (Blue Ash, OH)
- **Technical Writer ** Kelly Outsourcing Consulting Group has an opening for a **Technical Writer ** for a long-term engagement at one of our Global medical device ... team members. If you're passionate about bringing the latest scientific discoveries to life and are ready to take...data and information into a format that meets preclinical regulatory document requirements. + Develop charts, graphs, and data… more
- Bausch Health (Bridgewater, NJ)
- …skills and values drive our collective progress and impact. The Senior Medical Writer will have oversight of internal and external medical writing activities, create ... + Works with project teams to prepare clinical and regulatory documents, including protocols, study reports, investigator brochures, INDs/IMPDs, and… more
- BioFire Diagnostics, LLC. (Hazelwood, MO)
- Position Summary & Responsibilities: The Technical Writer is responsible for the development, revision, and control of product labeling deliverables (user manuals, ... 98development process and Lifecyle Management. During this process, the Technical Writer will write/update, review, and finalize labeling deliverable according to … more
- Actalent (Cranbury, NJ)
- …Title: Technical WriterJob Description We are looking for a Technical Writer responsible for developing, reviewing, and maintaining technical documents related to ... ARD/QC operations. This role ensures compliance with regulatory guidelines (FDA, ICH, USP, EP, cGMP) and in-house...Strong attention to detail and ability to translate complex scientific information into clear documentation. + Ability to work… more
- Charles River Laboratories (Wilmington, MA)
- …a career that you can feel passionate about. **Job Summary** The **Proposal Writer ** will work with sales and operations to coordinate and execute the provision ... put into centralized databases and repositories. This client-facing role requires scientific expertise, superior attention to detail, and excellent customer service… more
- Cambrex High Point (Charles City, IA)
- …for retirement, and more! Your Future Matters. Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality ... Matter by applying today! Job Overview The AD Technical Writer will be responsible for consistently generating high quality...and regulators. Compliance with SOPs, cGMP, ICH, and other regulatory guidelines is required to perform most job tasks.… more