- Exela Pharma Sciences, LLC (Lenoir, NC)
- …Training team, with additional input from Functional Area Managers (FAMs). The Technical Writer I will ensure regulatory compliance, and will collaborate with ... Position Summary The Technical Writer I is responsible for researching, writing, and...expertise, as needed.Education Requirements BA or BS degree in scientific discipline, or related field, with a strong writing… more
- Aequor (Seattle, WA)
- Job Description: Job Title: Technical Writer Schedule: M-F, Normal business hours, 100% Onsite Top Skills: Bachelor's degree in a relevant scientific field (eg, ... equivalent combination of education and experience preferred. Proven experience as a technical writer or in a related role within a clinical laboratory or regulated… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …investigation report contains the technical merit and completeness according to regulatory expectations. The Deviation Investigator- Writer will be responsible ... career. Are you ready to realize your potential? The PositionThe Deviation Investigator- Writer is responsible for investigating and writing of deviations to the… more
- Merck & Co. (North Wales, PA)
- …company's process es and standards to ensure compliance with internal policy, regulatory requirements, and health literacy principles . - Under the supervision of ... negotiating content with internal and external reviewers to ensure it meets regulatory requirements while leading the summary through review and final approval -… more
- Merck & Co. (Rahway, NJ)
- …lead clinical scientist on the clinical trial team.Collaborates with the Medical Writer on clinical/ scientific and regulatory documents.Partners with Study ... Job DescriptionJob SummaryThis position drives scientific planning, strategy and execution of Phase 1-4 clinical studies. Under the direction of the Program Lead,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …by leveraging our world-class science and technology. With more than 120 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and ... and immune disorders. Job Summary: The Associate Director of Regulatory Writing is a key role responsible for producing...role will also contribute to strategic planning and provide scientific and strategic insights at the study team level.… more
- ThermoFisher Scientific (Collegeville, PA)
- …biopharmaceutical company, all while maintaining full-time benefits. Discover Impactful Work: The Scientific Writer assists in the preparation and review of ... moderately sophisticated analytical methods, reports and protocols for potential submission to regulatory authorities. A day in the Life: + Prepares and/or assists… more
- Harvard University (Cambridge, MA)
- Details Title Scientific Writer /Project Manager (Research Associate) School Harvard Medical School Department/Area Department of Microbiology Position ... Description We are seeking a Scientific Writer /Project Manager (Research Associate) to provide...and that documents are error-free and follow formatting and regulatory requirements. * Prepare scientific illustrations; assemble… 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
- University of Miami (Miami, FL)
- …of Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time Scientific Writer to work at the UHealth Medical Campus. The Scientific ... The role requires a strong background in grant writing and scientific manuscript development. Primary Responsibilities: + Creates, implements, and maintains… more
- Danaher Corporation (Miami, FL)
- …science and patient care? Then read on! We are currently seeking a Medical and Scientific Writer who will be responsible for supporting our global Medical and ... to empower those seeking answers to life's most important scientific and healthcare questions. With a legacy spanning 80+...plus if you also possess previous experience in: + Regulatory submissions + Market access research understanding At Beckman… more
- Kelly Services (Sunnyvale, CA)
- Kelly(R) Science & Clinical is currently recruiting for a Technical Writer for a 6-month contract opportunity with a leading molecular diagnostics company at their ... Sunnyvale, CA. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career,… more
- MD Anderson Cancer Center (Houston, TX)
- …patient education/materials, IRB forms. Works collaboratively with research nurse manager and regulatory staff to develop or coordinate the development of the study ... patient education/materials, IRB forms. Works collaboratively with research nurse manager and regulatory staff to develop or coordinate the development of the study… more
- McLaren Health Care (Detroit, MI)
- **Position Summary:** **The Scientific /Medical Writer ** plays a critical role in the development and execution of Karmanos Cancer Institute (KCI) oncology ... of a clinical trial. This role requires a combination of scientific knowledge, attention to detail, and excellent writing skills. **Responsibilities** **:**… more
- Randstad US (Worcester, MA)
- scientific technical writer , qc micro. + worcester , massachusetts + posted today **job details** summary + $24 - $26.90 per hour + contract + bachelor degree + ... QC team members and SMEs to gather and interpret scientific data. + Compile data and author validation reports...and other technical documents in accordance with QC and regulatory requirements. + Format and prepare reports for submission… more
- Kelly Services (Deerfield, IL)
- …Responsibilities:** + With oversight, develops high quality clinical documents ensuring scientific excellence and regulatory compliance. + The development ... & Clinical** **(R)** is seeking an experienced Sr. Medical Writer for a short term contract with a Global...writing skills. + 5 years of on-the-job experience in scientific /medical writing eg, clinical trial and regulatory … more
- MicroVention, Inc. (Aliso Viejo, CA)
- **12251BR** **Title:** Sr. Medical Writer (PhD or MD) **Job Description:** **INNOVATION STARTS WITH YOU** Are you interested in working for an organization that is ... **TERUMO** has to offer. **Position Overview** The Sr. Medical Writer /Medical Writer will act as primary contact...job duties include: + Collaborating with the clinical & regulatory teams to write clinical documents for regulatory… more
- Publicis Groupe (Philadelphia, PA)
- …inspire HCPs, and ultimately lead to improved patient outcomes. Given our scientific and medical talent, powerful data warehouse and creative digital solutions, we ... current clients are excited about a more modern medical communications and scientific exchange that delivers a future-forward customer experience and meets the… more
- Astellas Pharma (South San Francisco, CA)
- **Nonclinical Scientific Writer -Bioanalytics** Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we ... www.astellasgenetherapies.com. **The Role:** In this role as a nonclinical Bioanalytics writer in Astellas Gene Therapy (AGT) group, you will perform supporting… more
- System One (Bothell, WA)
- Job Title: Technical Writer Location: Bothell, WA Hours/Schedule: M-F, Normal business hours Compensation: $22.25 - $28.20/hr Type: Contract, Potential for extension ... documents, and corrective and preventive action (CAPA) plans in accordance with regulatory standards and company policies. + Deviation Management: + Collaborate with… more
