- Novo Nordisk Inc. (Plainsboro, NJ)
- …for 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 ... requirements of a clinical program. Relationships The Senior Medical Writer reports to a Director of...7+ years of relevant experience Minimum of 5 years clinical/ regulatory medical writing experience in a pharmaceutical,… more
- Eisai, Inc (NJ)
- …you. Job Summary The Senior Manager, Medical Writing will be the designated Lead Medical Writer for approximately 3-4 Programs. As the Lead Medical ... At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides...as briefing books, Global Investigator Brochures (GIB) and annual regulatory reportsPrepare and review marketing application submission documentsAt the… more
- Tris Pharma (Monmouth Junction, NJ)
- …more studies, as neededCollaborates with assigned Clinical Research Organization (CRO) and/or Medical Writer to contribute to drafting of clinical study reports ... trial data and translates data into actionable plans at product levelContributes to Medical aspects of Regulatory issues related to development compounds or… more
- Merck & Co. (North Wales, PA)
- …as the lead clinical scientist on the clinical trial team.Collaborates with the Medical Writer on clinical/scientific and regulatory documents.Partners with ... set up and design during study start up (eg, database set up)Lead medical monitoring team in review and interpretation of clinical data/ medical … more
- BeiGene (San Mateo, CA)
- … Writer -- at a minimum 4 years' relevant industry experience as a regulatory medical writer , plus a BA/BS degree; PhD/PharmD in life sciences preferred. ... The Senior Medical Writer is responsible for writing,...+ Ensure clinical documents adhere to BeiGene standards and regulatory guidelines + Coordinate and manage contract medical… more
- MicroVention, Inc. (Tustin, CA)
- …experience in the development of regulatory / clinical submissions (preferably as a medical writer for pharmaceutical, CRO, or medical device clients). 4. ... **12078BR** **Title:** Sr. Medical Writer **Job Description:** **INNOVATION STARTS...documents and scientific presentations in cooperation with the Clinical, Medical , & Regulatory Affairs Teams, KOLs and… more
- Abbott (St. Paul, MN)
- …a Senior Clinical Evaluation Reporting / Medical Writer (CER). The Medical Writer on our Regulatory Clinical Evaluation team provides technical and ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Citigroup (Tampa, FL)
- The Regulatory Response Writer Senior Lead is a strategic professional who closely follows latest trends in own field and adapts them for application within own ... experts to inform these documents. + Oversee and manage key regulatory interactions (quarterly progress reports, formal examinations, on-going supervisions, ad-hoc … more
- Abbott (Santa Clara, CA)
- …from routine fingersticks. **The Opportunity** The function of a **Senior Medical Writer /Project Manager** supporting our Structural Heart Clinical Evaluation ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Medical Mutual of Ohio (OH)
- …financial data, understand trend and formulate recommendations on coverage under the medical plan. **Sr Healthcare Analyst- Policy Writer ** **Education and ... Founded in 1934, Medical Mutual is the oldest and one of...Cleveland, Ohio area residents preferred._** **Responsibilities** **Healthcare Analyst- Policy Writer ** + **Researches and analyzes evidence and background materials… more
- Novo Nordisk (Plainsboro, NJ)
- …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...years of relevant experience + Minimum of 5 years clinical/ regulatory medical writing experience in a pharmaceutical,… more
- Novo Nordisk (Lexington, MA)
- …clinical development and regulatory requirements of a clinical program. The Medical Writer performs work independently under the supervision of more ... to develop new medicines for patients. The Position The Medical Writer works closely with cross-functional project...5+ years of relevant experience. Minimum of 3 years clinical/ regulatory medical writing experience in a pharmaceutical,… more
- Adecco US, Inc. (Bridgewater, NJ)
- …onsite at Bridgewater, NJ and few days for the first few months) Duties The CMC Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory ... such as white papers, position papers, and briefing book. In parallel, the technical writer could help support non regulatory writing projects such as SOP and… more
- ThermoFisher Scientific (Juneau, AK)
- **Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** **Senior Medical Writer (North America) (FSP; Remote)** At Thermo ... in North America. We are looking for a Senior Medical Writer to be dedicated to a...the use of software for document development, document types, regulatory requirements, and therapeutic area knowledge. + Ensures compliance… more
- Actalent (Gaithersburg, MD)
- Pharmaceutical company seeking an experienced Medical Writer with both clinical and regulatory writing expertise. Applicants must be located on the East ... Coast. Position Summary: The Medical Writer will work with the clinical and regulatory teams to prepare regulatory submissions, protocols including… more
- IQVIA (Ithaca, NY)
- We are seeking a ** Medical Writer ** to join Q2 Solutions, IQVIA's laboratory business **Remotely.** We hire passionate innovators who drive healthcare forward ... we transform and accelerate research and development. As a Medical Writer , you will contribute to the...staff. + Keep abreast of current data, trends, scientific writing/ regulatory knowledge, developments, and advances in area of drug… more
- Abbott (Plano, TX)
- …of 3 plus years of progressively more responsible experience as a technical writer in a medical or high technology (preferably biotechnology) environment. + ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Kelly Services (Gillette, WY)
- ** Medical Writer ** Kelly(R) Science & Clinical is seeking a Medical Writer for a direct-hire position at a leading client in the Stem Cell Research ... cell research company known for its innovative solutions and high-quality standards in medical writing and clinical research. In this role, you'll be working with a… more
- Abbott (Santa Clara, CA)
- …generic medicines. Our 114,000 colleagues serve people in more than 160 countries. **Principal Medical Writer ** **Working at Abbott** At Abbott, you can do work ... join our rapidly growing clinical team within the SH division. The Principal Medical Writer will be responsible for producing podium presentations, scientific… more
- Cook Medical (West Lafayette, IN)
- …development. CRI is currently accepting applications for a Scientific Communications Scientist (ie, Medical Writer ) to become a part of our growing Scientific ... process; + Provide status updates on deliverables to management; + Understand medical writing and regulatory standards and practices; + Proactively contribute… more
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