- 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. (Foster City, CA)
- …care of patients with life-threatening diseases. We are seeking a talented Scientific Publication Medical Writer with specialized experience in Viral Hepatitis, ... This position is located at our Headquarters in Foster City, CA. ** Scientific Publications Medical Writer :** + Collaborate with cross-functional teams to… more
- ThermoFisher Scientific (Wilmington, NC)
- …Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** **Senior Medical Writer (NA) (FSP; Remote)** At Thermo Fisher Scientific , ... **Summarized Purpose:** We are looking for a Senior Medical Writer to work embedded with one of our clients...the FSP team, you will provide high-quality medical and scientific writing from planning and coordination through delivery of… 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
- Kelly Services (North Charleston, SC)
- …technical documents including study protocols, reports, SOPs, work instructions, and regulatory submissions + Collaborate with scientific and operational teams ... **Technical Writer - 6-Month Contract (Fully Onsite)** **Location:** Morrisville,...The ideal candidate will have experience creating and managing scientific and technical documentation in a regulated environment, particularly… 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
- ICON Clinical Research (Blue Bell, PA)
- … Writer will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical ... Principal Medical Writer - United States (Remote) ICON plc is...clinical trial results as well as developing submissions to regulatory authorities and ensuring compliance with industry standards. Responsibilities… more
- ICON Clinical Research (Blue Bell, PA)
- …ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical ... Principal Medical Writer - Remote ICON plc is a world-leading healthcare...will be crucial in supporting our clients' submissions to regulatory authorities and ensuring compliance with industry standards. **What… 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
- 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
- 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
- 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