• Process Engineer/ Technical Writer

    ThermoFisher Scientific (Allentown, PA)
    …knowing that what they do matters. **What will you do?** Our company seeks a Technical Writer and Investigator , that investigates and responds to Quality ... and demonstrates and promotes the company vision. + Composes technical concepts in a clear and concise manner and...Abilities** + Strong written and verbal communication to convey technical concepts clearly and concisely with good punctuation and… more
    ThermoFisher Scientific (09/13/24)
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  • Deviation Investigator - Writer

    Novo Nordisk (West Lebanon, NH)
    …career. Are you ready to realize your potential? The Position The Deviation Investigator - Writer is responsible for investigating and writing of deviations to the ... merit and completeness according to regulatory expectations. The Deviation Investigator - Writer will be responsible for initiating investigations and writing… more
    Novo Nordisk (09/05/24)
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  • Technical Writer (Scientific…

    MD Anderson Cancer Center (Houston, TX)
    …and the public. **SUMMARY** Writes, edits and coordinates production of highly technical medical material. Retrieves data from databases and other internal and ... Mentors staff. **JOB SPECIFIC COMPETENCIES** Protocol Writing Assists the Principal Investigator with developing, writing and editing protocol documents for … more
    MD Anderson Cancer Center (09/07/24)
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  • College of EMS - Grant Writer

    Pennsylvania State University (University Park, PA)
    …The College of Earth and Mineral Sciences (https://www.ems.psu.edu/) (EMS) is seeking a Grant Writer ( Technical Writer - Intermediate Professional) to play a ... APPLICATION INSTRUCTIONS: + CURRENT PENN STATE EMPLOYEE (faculty, staff, technical service, or student), please login to Workday to complete the internal application… more
    Pennsylvania State University (09/08/24)
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  • Senior Grant Writer

    University of Southern California (Los Angeles, CA)
    …(https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/Senior-Grant- Writer \_REQ20133166/apply) Keck School of Medicine Los ... of Medicine of USC seeks an experienced Senior Grant Writer to research, draft, and submit proposals to support...a history of submitting NIH grants as a principal investigator . This position will report to the Operations &… more
    University of Southern California (07/30/24)
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  • Grant Writer

    Suny Polytechnic Institute (Utica, NY)
    …of figures and other graphical elements. Work may include being the lead writer on non- technical applications. + Identify resources both internal and external ... Professional Posted On: Tue Jul 23 2024 Job Description: The Grant Writer will identify funding opportunities, draft proposals, prepare supporting documentation and… more
    Suny Polytechnic Institute (07/25/24)
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  • Scientific Writer - Clinical Orthopedics

    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 ... communications venues. **PEOPLE ESSENTIAL FUNCTIONS** + Works with principal investigator , provides advice on grantsmanship, editorial support and standardized… more
    Houston Methodist (08/06/24)
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  • Sr Technical Writer

    MD Anderson Cancer Center (Houston, TX)
    Provides technical writing and editing of grants, publications, clinical research proposals, and clinical trial protocols. Impacts the visibility of melanoma ... projects concurrently and, through excellent communication skills, deliver high-quality technical content for both internal and external publication. 2. Demonstrated… more
    MD Anderson Cancer Center (09/07/24)
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  • Sr. Medical Writer /Medical Writer

    Kelly Services (Deerfield, IL)
    **Kelly Science & Clinical** **(R)** is seeking an experienced Sr. Medical Writer for a short term contract with a Global Biotech Company. **Job Title: Sr. Medical ... Writer Specialist in Worldwide Medical Advanced Surgery** **Job Description:**...ensuring delivery within timelines. + Clinical documents may include investigator brochures, protocols, clinical study reports, integrated reports, clinical… more
    Kelly Services (09/07/24)
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  • QC Analytical Investigator

    Insight Global (Boston, MA)
    …management experience, comfortable managing multiple stakeholder relationships . Strong technical writer with previous experience authoring, reviewing and ... Description Insight Global is looking for a QC Analytical Investigator to sit on-site at a brand new facility...through Friday. This position will be supporting the growing technical services team in their risk assessment efforts. This… more
    Insight Global (08/06/24)
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  • Regulatory, Clinical, and Technical

    Alaka'ina Foundation Family of Companies (Frederick, MD)
    …Regulatory Scientist; Technical Writer ; Program Manager; Biomedical Science Writer ; Principal Investigator . + Medical Services - a . Positions may ... Regulatory, Clinical, and Technical Clinical Trial support Location MD - Frederick...need for top talent to provide Regulatory, Clinical, and Technical Clinical Trial support services to a DoD biomedical… more
    Alaka'ina Foundation Family of Companies (07/17/24)
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  • Grants and Contracts Coordinator

    Institute for Medical Research (Durham, NC)
    …pre-award research planning for clinical research studies conducted by the Principal Investigator , Dr. Stephen Freedland, and his associates in his urology research ... lab. Grants and Contracts Coordinator will report to the Proposal and Grant Writer Team Lead or designee. The successful candidate will have the opportunity to be… more
    Institute for Medical Research (08/31/24)
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  • Director, Medical Monitor, Vaccines

    Pfizer (Collegeville, PA)
    …requirements, clinical plan expectations, and study timelines; this includes ensuring medical/ technical requirements for data integrity are applied. + Works with ... statistician, and delivery of clinical study report in collaboration with medical writer and accountable for overall quality and timeliness of analysis and… more
    Pfizer (08/31/24)
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  • Sr. Medical Writing Specialist

    ManpowerGroup (Deerfield, IL)
    Our client in pharmaceutical Industry is seeking a Sr Medical Writer to join their team. The ideal candidate will have experience in scientific or clinical ... which will align successfully in the organization. **Job Title: Senior Medical Writer ** **Location: Fully Remote** **Pay Range: $70/hr - $78/hr** **What's the Job?**… more
    ManpowerGroup (09/05/24)
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  • Senior Analyst, Immunology Regulatory Medical…

    J&J Family of Companies (Columbus, OH)
    …documents such as, but not limited to, clinical study reports, investigator 's brochures, study protocols, summary documents, risk management plans, regulatory ... and clinical team, as needed. + If a lead writer for a program: Be the primary point of...medical writing experience is required. + Authoring experience with investigator brochures, clinical study protocols, and clinical study reports.… more
    J&J Family of Companies (06/24/24)
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  • Associate Director, Medical Monitor

    Pfizer (Collegeville, PA)
    …requirements, clinical plan expectations, and study timelines; this includes ensuring medical/ technical requirements for data integrity are applied. + Works with ... statistician, and delivery of clinical study report in collaboration with medical writer and accountable for overall quality and timeliness of analysis and… more
    Pfizer (07/12/24)
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  • Senior Director, Vaccine Clinical Research…

    Pfizer (Pearl River, NY)
    …related to clinical research programs. The clinician medical monitor applies technical /scientific expertise to resolve problems regarding the clinical components of ... documents (eg, Investigational New Drugs, New Drug Applications/Common Technical Documents, global registration dossiers, lifecycle strategy documents, internal… more
    Pfizer (08/30/24)
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  • Senior Manager, Medical Writing

    BeiGene (San Mateo, CA)
    …but are not limited to study reports, clinical study protocols or amendments, investigator brochures, and clinical sections of INDs, NDAs, MAAs and other regulatory ... INDs, MAAs, and NDAs is a plus + The technical /scientific ability to critically analyze, synthesize, and present complex...years of relevant industry experience as a regulatory medical writer with a BA/BS degree. All qualified applicants will… more
    BeiGene (07/18/24)
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