• Merck & Co. (North Wales, PA)
    …Senior Director of Global Health Literacy & Health Equity is the enterprise lead for establishing our company as an industry leader and sought-after partner in ... Development Division Serve as an expert on informed consent policy and lead assessment/implementation of policy changes while integrating health literacy, and health… more
    HireLifeScience (01/03/25)
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  • Lead Corporate Investigator

    Lumen (Trenton, NJ)
    …standards that govern our business conduct. Our team is seeking a full-time Lead Corporate Investigator to conduct internal investigations into concerns ... investigations, and will otherwise support the Ethics and Compliance team. The Corporate Investigator role in the organization is critical to the success of the… more
    Lumen (01/09/25)
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  • Associate Director, Clinical Operations

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …accountability for operational study-level timeline, cost, and quality deliverables. + Lead the development of the clinical study plan including critical path ... for assigned clinical stud(ies) utilizing Microsoft Project or equivalent. + Lead the creation of the cross functional Clinical Study Oversight Plan… more
    Daiichi Sankyo Inc. (01/08/25)
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  • Sr. Director, Global Heath Literacy & Health…

    Merck (North Wales, PA)
    …The Senior Director of Global Health Literacy & Health Equity is the enterprise lead for establishing our company as an industry leader and sought-after partner in ... Division + Serve as an expert on informed consent policy and lead assessment/implementation of policy changes while integrating health literacy, and health equity… more
    Merck (01/03/25)
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  • Senior Security Professional

    PPL Corporation (Allentown, PA)
    …communities today. Overview This senior level position is responsible for supporting corporate services and all operating companies with a broad range of duties, ... including but not limited to promoting physical security, corporate emergency preparedness and response, security compliance requirements, conducting investigations,… more
    PPL Corporation (12/03/24)
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  • Medical Director, Endocrine Medical Sciences (US…

    Ascendis Pharma (Princeton, NJ)
    …focus/expertise in these areas is a major advantage. The candidate is expected to lead key strategic, cross-as well functional projects as part of the US Medical ... phase IV clinical programs including, patient registries, and oversight of investigator -initiated Studies (IISs) as well as Special access programs. The candidate… more
    Ascendis Pharma (12/10/24)
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  • Oncology Regional Medical Scientific Director…

    Merck (Trenton, NJ)
    …for approved, in-development, and active Company-sponsored trials and/or investigator -sponsored research studies. The Regional Medical Scientific Director serves ... Enhances the comprehension of the scientific foundations and goals of investigator -sponsored research + Identifies barriers to patient enrollment and retention… more
    Merck (01/09/25)
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  • Regional Medical Scientific Director | Immunology…

    Merck (Trenton, NJ)
    …and goals for approved, in-development, and active Company-sponsored trials and/or investigator -sponsored research studies and serve as a role model for other ... and/or sharing of therapeutic expertise. Consistent adherence to field and corporate policies and Global Medical Scientific Affairs (GMSA) strategy, including field… more
    Merck (11/13/24)
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  • Director, Medical Affairs Strategy…

    Sumitomo Pharma (Trenton, NJ)
    …evaluation, motivation, and control of activities in alignment with the company's corporate strategies and objectives. + Lead cross-functional medical alignment ... post-launch activities related to Medical Affairs function. This individual will lead program coordination with Clinical Development leadership to ensure alignment… more
    Sumitomo Pharma (11/27/24)
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  • Director, Clinical Operations (Oncology)

    Gilead Sciences, Inc. (Parsippany, NJ)
    …that supports global registration and commercialization of Gilead's products. You will typically lead a large team of direct and indirect reports. You will be ... of resources to support a fluid 'One Ops' workforce. You will lead and/or effectively engage in Clinical Operations, cross-functional and/or country or regional… more
    Gilead Sciences, Inc. (01/08/25)
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  • Manager, R&D Quality Assurance

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …in a perpetual state of compliance as follows: + Support the Global Quality Lead (s) (GQLs) and Regional Quality Leads (RQLs), who are responsible for the delivery ... meetings or other relevant activities. + Support the External Partner Quality Lead (s) (EPQLs), who are responsible for delivering and executing Quality Oversight… more
    Daiichi Sankyo Inc. (12/02/24)
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  • Executive Director Head of Medical Strategy

    Sumitomo Pharma (Trenton, NJ)
    …team and play a highly visible role internally and externally, and effectively lead and communicate with cross-functional team members to develop and execute the ... to Global/Sumitomo Pharma America Inc. R&D Strategy and other corporate functions. ​ + Provide input to VP Medical...costs to keep within budget of Medical Affairs. + Lead , develop and mentor team members​. + Specify, develop… more
    Sumitomo Pharma (12/05/24)
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  • Director, Medical Affairs Strategy (Women's…

    Sumitomo Pharma (Trenton, NJ)
    …internal company programs and external facing interactions. This job will effectively lead and communicate with cross-functional team members to share and gain ... to HCP stakeholders and healthcare payers. + Serve as a Medical Strategy lead for the Pfizer alliance for Women's Health, ensuring coordination and alignment of… more
    Sumitomo Pharma (11/21/24)
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  • Senior Director, Oncology R&D

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …May review tables, listings, and figures (TLF) and CSR safety narratives + May lead the development and updates of the Investigator 's Brochure (IB): author the ... **Clinical Development Expertise Strategy:** + In collaboration with the Global Clinical Lead (GCL), if applicable, leads the development and execution of the… more
    Daiichi Sankyo Inc. (01/01/25)
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  • Sr. Medical Director, Medical Affairs

    Taiho Oncology (Princeton, NJ)
    …on current focused therapeutic area issues and questions + Set up and lead advisory boards + Review investigator -sponsored study (IIST) proposals and other ... understanding of all areas and functions within medical affairs and able to lead strategic development of the integrated Medical Affairs Plan (iMAP). Having the… more
    Taiho Oncology (11/27/24)
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  • Senior Director, Head of Medical Review

    Bristol Myers Squibb (Princeton, NJ)
    …Area Heads / Directors within Medical Safety Review. Takes the global lead in assuring consistent application of work practices and processes. Delegates to ... input the development of the Reference Safety Information section of the Investigator 's Brochure; provides peer review for safety documents (RMP, IB, aggregate… more
    Bristol Myers Squibb (01/08/25)
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  • Executive Director, Medical Affairs, Ophthalmology

    Merck (Trenton, NJ)
    …execution of scientific & medical affairs plans for Ophthalmology). They build and lead a team of TA dedicated global and regional directors and associate directors. ... data generation studies with V&I Outcomes Research + Supports the Investigator -Initiated Study program + Leads talent review process and demonstrates follow-through… more
    Merck (12/14/24)
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  • Senior Director, Medical Affairs Strategy (Rare…

    Sumitomo Pharma (Trenton, NJ)
    …multiple specialist types in a complex care setting. This job will effectively lead and communicate with cross-functional team members to share and gain insights ... research and presents research concepts to internal Review Committee for Investigator Initiated Study (IIS) concepts and research protocols. + Leads internal… more
    Sumitomo Pharma (11/21/24)
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  • GCP QA Auditor II- fully remote!

    ThermoFisher Scientific (Allentown, PA)
    …site audits, laboratory and file audits for clients and projects. Lead process/quality improvement initiatives. Mentor peers. Develop tools and other materials ... of the clinical trial process * Experience with study-specific ( investigator site) audits or other GP audits, could also...license and ability to qualify for and maintain a corporate credit card with sufficient credit line for business… more
    ThermoFisher Scientific (01/09/25)
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