- Cardinal Health (Sacramento, CA)
- …Ensure accurate and timely completion/delivery of information and review of regulatory submissions . Communicate deliverables needed and corresponding writing ... Medical Writing bring to Cardinal Health:_** Full-service product development and regulatory affairs consulting team that enables pharmaceutical, medical and… more
- Cordis (Irvine, CA)
- …documentation, including Instructions for Use (IFUs), to support our product compliance and regulatory submissions . As a Technical Writer within the ... current documentation is accessible and properly archived for audits and regulatory submissions . **Qualifications** + **Education:** Bachelor's degree in… more
- Novo Nordisk (Lexington, MA)
- …high level strategic input into development plans, study designs, and regulatory submissions . Relationships The Principal Medical Writer reports to a ... ready to make a difference? The Position The Principal Medical Writer is an expert in ...into documents and plans to support clinical operations and regulatory submissions across a range of development… more
- University of Miami (Miami, FL)
- …- 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 data and translates complex scientific concepts,...of clinical trials including protocol and ICF development, institutional regulatory submissions (Protocol Review and Monitoring Committee… more
- Arvinas (New Haven, CT)
- … Medical Writer is responsible for development and management of medical writing deliverables that support the clinical regulatory writing portfolio and ... capable of working independently to achieve goals. The Director, Medical Writer is responsible for leading a...plans and managing projects, to complete multiple documents for regulatory submissions and clinical deliverables. + Provide… more
- Novo Nordisk (Lexington, MA)
- …a living. Are you ready to make a difference? The Position The Senior Medical Writer works closely with cross-functional project teams to manage preparation of ... requirements of a clinical program. Relationships The Senior Medical Writer reports to a Director of...QC review of documents to support clinical trials and regulatory submissions , which may include: + Clinical… more
- MicroVention, Inc. (Aliso Viejo, CA)
- **12251BR** **Title:** Sr. Medical Writer (PhD or MD) **Job Description:** **INNOVATION STARTS WITH YOU** Are you interested in working for an organization that ... (R) **TERUMO** has to offer. **Position Overview** The Sr. Medical Writer / Medical Writer ... regulatory teams to write clinical documents for regulatory submissions , including but not limited to:… more
- System One (San Rafael, CA)
- Job Order #: 329444 Title of Position: Medical Writer Location: San Rafael, CA Type: Contract Pay Rate: $50-$54/hr. W2 ONLY (NO STEM OPT CANDIDATES) Hybrid (1-2 ... days in office to align with company policy). The Contract Medical Writer applies advanced documentation preparation and document project management skills to… more
- Houston Methodist (Houston, TX)
- … agency requirements. + Prepares moderately complex documents and sections of regulatory submissions and contributes scientific knowledge and analytical skills ... The Scientific Writer at Houston Methodist, Department of Digital Health...preparation of grant proposals, manuscripts, presentations, protocols, and clinical regulatory documentation. + Assures quality and timely preparation of… more
- Houston Methodist (Houston, TX)
- …ESSENTIAL FUNCTIONS** + Prepares moderately complex documents and sections of regulatory submissions and contributes scientific knowledge and analytical skills ... At Houston Methodist, the Senior Scientific Writer is responsible for functioning as the mentor...for junior staff with an extensive knowledge of both medical and technical science while working with scientific and… more