- BeOne Medicines (Emeryville, CA)
- …Education/Experience Required: + At a minimum 4 years' relevant industry experience as a regulatory medical writer with a BA/BS degree; PhD/PharmD in life ... **General Description:** The Senior Medical Writer is responsible for writing,...+ Ensure clinical documents adhere to BeOne standards and regulatory guidelines. + Coordinate and manage contract medical… more
- Terumo Neuro (Aliso Viejo, CA)
- …experience in the development of regulatory / clinical submissions (preferably as a medical writer for pharmaceutical, CRO, or medical device clients). 4. ... **12640BR** **Title:** Sr. Medical Writer **Job Description:** **INNOVATION STARTS...documents and scientific presentations in cooperation with the Clinical, Medical , & Regulatory Affairs Teams, KOLs and… 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 ... closely with clinical development teams, including clinical scientists, clinical affairs, regulatory affairs, biostatistics, physicians, and medical affairs, to… 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 [PRMC] and… more
- ICON Clinical Research (New York, NY)
- Medical Writer II- Farmingdale, NY- Hybrid ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an ... you to join us on our mission to shape the future of clinical development. ** Medical Writer II- Farmingdale, NY- hybrid work pattern** We are currently seeking a… more
- Kelly Services (Bloomington, IN)
- Technical Writer (Bloomington, IN) Our client in the medical devices/ life sciences/pharma space, is currently in need of a Technical Writer for a large ... or capped end date, however, this project is expected to take 3-6 months. Technical Writer will need to sit onsite in at the client's facility in Bloomington, IN, as… more
- System One (New Haven, CT)
- Job Title: Medical Writer (part time) Location: Northeast (EST) candidates preferred Hours: 30 hours/month (7-8 hours/week) Type: Contract (C2C or W2) Job ... Purpose The Translational Research Medical Writer plays a key role in...clinical research teams (Chemistry, Clinical, Quality Assurance, Project Management, Regulatory , Image Analysts, Scientists, Investigators, Operations, Medical … more
- AbbVie (San Francisco, CA)
- …Aesthetics | An AbbVie Company Job Description Purpose The medical writer is responsible for providing clinical regulatory document support to clinical ... submission-ready documents and effective implementation of the clinical writing process. The medical writer : provides medical writing expertise for multiple… more
- Eurofins (Lancaster, PA)
- …origin, traceability and purity of biological substances and products. Technical Writer : Manage the production of simple scientific and technical documents ... technical documents, training material and other written material. Senior Technical Writer : Manage the production of complex scientific and technical documents… more
- System One (Armonk, NY)
- Title: Senior Medical Writer Location: Armonk, NY (hybrid) Duration: 9 month contract, possible to renew Pay range: $65-75/HR Start Date: ASAP The Senior ... Medical Writer (SMW) works with team members...variety of therapeutic areas. Opportunities to contribute to other regulatory documents may be provided. The SMW tracks his/her… more
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