- Nanobiosym, Inc. (Cambridge, MA)
- Cambridge, MA, USA | Contract Job Title: Scientific Writer (Onsite Consultant)Location: Cambridge, MA About the Role: We are seeking an experienced Scientific ... Writer with a strong background in scientific editing and publication to support our research and communications team. The ideal candidate will have a PhD or… more
- University of Miami (Miami, FL)
- …of Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time Hybrid Scientific Writer 2 to work at the UHealth medical campus in Miami, Fl. ... CORE JOB SUMMARYThe Hybrid (1X a week or as necessary) Scientific Writer 2 collects and analyzes complex scientific data and concepts within a variety of… more
- Houston Methodist (Houston, TX)
- The Houston Methodist Peak Brain & Pituitary Tumor Center seeks a scientific writer . The scientific writer will primarily be responsible for proofreading ... ESSENTIAL FUNCTIONS** + Prepares moderately complex documents and sections of regulatory submissions and contributes scientific knowledge and analytical skills… more
- Houston Methodist (Houston, TX)
- At Houston Methodist, the Scientific Writer position is responsible for performing a variety of tasks including preparing laboratory and clinical studies and ... agency requirements. + Prepares moderately complex documents and sections of regulatory submissions and contributes scientific knowledge and analytical skills… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …care of patients with life-threatening diseases. We are seeking a talented Scientific Publication Medical Writer with specialized experience in Viral Hepatitis, ... our Headquarters in Foster City, CA or in our Parsippany, NJ office. ** Scientific Publications Medical Writer :** + Collaborate with cross-functional teams to… 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
- Sanofi Group (Morristown, NJ)
- **Job Title:** Associate Director-Principal Medical Writer **Location:** USA, Remote. Proximity to Cambridge/Boston, MA or Morristown, NJ is highly desirable for ... skills could be critical in helping our teams accelerate progress. The Principal Medical Writer is a key member of the Medical Writing team, the Clinical Trial Team… more
- United Therapeutics (Research Triangle Park, NC)
- …You Are You are creative and detail-oriented with deep expertise in regulatory submissions and writing, including clinical study reports, clinical study protocols, ... and investigator's brochures. You also bring strong experience in external-facing scientific communications - such as manuscripts, posters, and abstracts - to… 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, ... **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
- University of Colorado (Aurora, CO)
- **Quality Control Analyst I Data Reviewer/Technical Writer ** **Description** **University of Colorado Anschutz Medical Campus** **Department: Gates Biomanufacturing ... Facility** **Job Title: Quality Control Analyst I - Data Reviewer/Technical Writer ** **Position #: 803791 - Requisition #:37813** **Job Summary:** Key… 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
- 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
- Envista Holdings Corporation (Brea, CA)
- **Job Description:** Ormco is seeking a talented and detail-oriented Technical Writer to join our dynamic Global Marketing team. In this crucial role, you will be ... material science, and technological advancements. Ensure accuracy, clarity, and scientific rigor in all technical documentation. + Creating White Papers:… more
- Actalent (Lexington, MA)
- Job Title: Medical Writer Job Description This role involves the review and preparation of clinical and regulatory documents to ensure compliance with ... of document types according to standard operating procedures, guidelines, and regulatory requirements. Responsibilities + Review and prepare clinical and … more