- Terumo Neuro (Aliso Viejo, CA)
- … scientific experience. 3. Demonstrated experience in the development of regulatory / clinical submissions (preferably as a medical writer for pharmaceutical, ... **12933BR** **Title:** Sr. Medical Writer (US Remote & Temp to Hire) **Job...job duties include: + Collaborating with the clinical & regulatory teams to write clinical documents for regulatory… more
- System One (New Brunswick, NJ)
- …Co-authors/ authors scientific content for CTD Quality sections aligned with regulatory strategy for clinical and life-cycle CMC regulatory submissions and ... Job Title: Pharma Technical Writer Location: New Brunswick, NJ Hours/Schedule: Mon-Friday (normal...to project timelines and aligned with CTD requirements and regulatory strategy. + Provide input and scientific … more
- Stryker (Fremont, CA)
- …Writer ,** you will work closely with cross-functional teams ( Regulatory , Clinical, Quality, Marketing) ensuring successful preparation of high-quality ... Stryker is currently seeking a **Staff Medical Writer ** to join our Neurovascular Division to be...Interprets literature information and synthesizes the information in clinical regulatory documents. + For all documents, coordinates and manages… more
- System One (Cleveland, OH)
- …related scientific discipline + Minimum of 6+ years of pharmaceutical regulatory medical writing and 3+ years of scientific /academic writing experience, and ... Job Title: Director / Senior Director Medical Writer Location: CST or EST candidates willing to...will include the successful preparation of high quality, submission-ready regulatory documents, reports and protocols through implementation of the… more
- Abbott (Plymouth, MN)
- … Writer will be responsible for producing abstracts, manuscripts, scientific publications, and clinical study reports. This position will work collaboratively ... position will: + Responsible and accountable for execution of presentations, scientific publications, clinical study report writing for regulatory submission… more
- Abbott (Maple Grove, MN)
- …for a **Senior Medical Writer , Clinical Evaluation** . The Sr. Medical Writer on our Regulatory Clinical Evaluation team provides technical and strategic ... products. Experience in clinical study management and design, medical, or scientific writing, and/or quality engineering/risk management and strong written and… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Principal Medical Writer Associate Director **Location** : USA, Remote. Proximity to Cambridge/Boston, MA or Morristown, NJ is highly desirable for ... serves to generate timely, high quality, cost effective and regulatory compliant documents. Our mission is to synergize and...You** **Core Experience** : + Six+ years as medical writer or equivalent specialist role + Proven track record… more
- Danaher Corporation (Miami, FL)
- …related discipline. . 0-2+ years experience or coursework in technical writing, regulatory affairs, or scientific communication. . Proficiency in Microsoft ... Reagent Labeling Writer Intern Accelerating answers Are you ready to...hands-on experience and exposure in the critical area of regulatory labeling within the medical device and Life Sciences… more
- University of Utah (Salt Lake City, UT)
- …**Job Title** Research Scientist **Working Title** Research Scientist, Protocol Writer **Career Progression Track** F **Track Level** **FLSA Code** Professional ... **Job Summary** Develops research projects and is responsible for scientific design, conduct and interpretation, presenting results and publishing manuscripts.… more
- Kelly Services (Barceloneta, PR)
- …job that works for you. How about this one? We're seeking an **Investigation Writer ** to work with one of our top global biopharmaceutical clients in the ... it's all about finding the job that's just right **Purpose:** The Investigator writer is responsible for providing quality assurance support for the plant including… more