• Medical Director - Medical Monitoring

    United Therapeutics (Research Triangle Park, NC)
    …of experience as a medical monitor in pharmaceutical product development within a clinical research organization or pharmaceutical company + MD - Physician - ... Microsoft Office software suite including Word/Excel/Outlook/PowerPoint + Previous experience performing a clinical research role within a clinical more
    United Therapeutics (09/04/25)
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  • Senior Principal Scientist, Project Team…

    Boehringer Ingelheim (Ridgefield, CT)
    Research Pharmacology, Drug Metabolism & Pharmacokinetics, Translational Medicine & Clinical Pharmacology, CMC, Regulatory Affairs , Patient Safety and ... is responsible for developing nonclinical safety strategies that support the clinical development plan in oncology and non-oncology indications. The NDS team… more
    Boehringer Ingelheim (07/10/25)
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  • Nurse Practitioner (NP)

    Hospice of Michigan (Traverse City, MI)
    …the Nurse Practitioner scope of practice. This could include collaboration on research , education, innovative clinical partnerships, and new business development ... time, expenses, supplies and labor and ensures pre-determined financial margins and/or clinical outcomes are achieved. + Provides support to physicians as needed,… more
    Hospice of Michigan (09/06/25)
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  • Technical Writer

    Envista Holdings Corporation (Brea, CA)
    …Collaboration: Work closely with product marketing, clinical affairs , research and development, sales, and regulatory teams to gather information, ensure ... clinicians globally to develop compelling case studies that highlight the clinical benefits and successful outcomes achieved with Ormco's clear aligner (Spark)… more
    Envista Holdings Corporation (07/11/25)
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  • Statistical Science Lead, Biomarker

    Astellas Pharma (Northbrook, IL)
    …data into clinical development plans. Their work helps bridge early research with clinical application, enabling data driven decision for patient ... treatment response, and patient stratification + Broad expertise across clinical trial statistics, exploratory statistics, Medical Affairs statistics,… more
    Astellas Pharma (09/10/25)
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  • Associate Director, Literature Analyst

    Merck (Boston, MA)
    …information clearly and concisely to diverse audiences, including researchers, clinicians, regulatory affairs professionals, and other stakeholders + Familiarity ... Adaptability, Biopharmaceutical Industry, Biopharmaceuticals, Biopharmaceutics, Boolean Searches, Change Management, Clinical Research , Communication, Cross-Functional Team Leadership, Data… more
    Merck (09/06/25)
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  • Associate Director, Pipeline & External Innovation…

    AbbVie (North Chicago, IL)
    …execution for scientific data disclosures (eg, congress presentations, publications), clinical development milestones, regulatory filings, and pre-commercial ... announcements. + Collaborate cross-functionally with R&D, Clinical , Medical Affairs , Commercial, and Alliance Management to ensure alignment and integration of… more
    AbbVie (08/29/25)
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  • Director of Public Policy

    State of Massachusetts (Boston, MA)
    …government relations and policy agenda. As a key member of the External Affairs team, the Director will lead initiatives that shape legislation, advocate for ... with other state agencies and report directly to the Chief External Affairs Officer at Children's Trust. *Key Responsibilities:* */Government Relations & Advocacy… more
    State of Massachusetts (07/03/25)
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  • Risk Safety Manager, Full Time, Mt.

    Virtua Health (Mount Holly, NJ)
    …will work collaboratively with key team members, Clinical Quality/Safety, Medical Affairs , and Regulatory Affairs departments in facilitating safety ... and standardization on Cause Analysis methodology. + Partners with clinical quality team to ensure patient safety goals are...and outside the organization + Excellent writing, speaking, and research skills + Analytical skills and the ability to… more
    Virtua Health (08/08/25)
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  • Data Governance - Compliance Specialist

    AbbVie (North Chicago, IL)
    …+ Bachelor's degree or above in life sciences, health law, business administration, regulatory affairs , or related field. + 4+ years' experience in ... review, edit, and optimize ICFs and consent documentation for regulatory compliance and sample management transparency. + Assist in...clinical research governance, protocol/sample management, or operations… more
    AbbVie (09/13/25)
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