• Sr Director Regulatory

    Baystate Health (Springfield, MA)
    Under the direction of the Chief Quality Officer, the Senior Director , Regulatory Affairs directs the strategic management and planning for the Joint ... activities for clinical services throughout Baystate Health, including all licensed sites. The Senior Director , Regulatory Affairs develops a… more
    Baystate Health (04/26/24)
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  • Sr . Clinical Affairs Manager,…

    Teleflex (Hartford, CT)
    …Interventional Urology is to manage the field based Clinical Affairs Managers. The Sr Manager will report to the Director of Clinical Affairs ... Affairs Manager. Activities will be assigned from the Director to the Sr . Managers and can...the Canadian Medical Device Regulations, and all other international regulatory requirements with which Teleflex complies. **Language and Verbal… more
    Teleflex (05/24/24)
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  • Sr . Thought Leader Liaison, Dermatology…

    Sanofi Group (Hartford, CT)
    …interactions are always within label, and consistent with commercial, compliance, legal and regulatory guidelines. A Sr . TLL will work closely, and within ... initiatives and provide timely feedback. TLLs will report directly to the Director , Dupilumab Dermatology. **JOB RESPONSIBILITIES:** The Sr . TLL job… more
    Sanofi Group (04/29/24)
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  • Chief Pharmacy Officer ( Senior

    The Cigna Group (Bloomfield, CT)
    **OVERVIEW:** The Chief Pharmacy Officer ( Senior Director ) oversees and directs the creation, adoption and evaluation of clinical pharmacy programs, product and ... integrity of the Health Plan pharmacy offering and completes associated regulatory attestations as required. + Works with Federal/State government affairs more
    The Cigna Group (04/30/24)
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  • Director , Health Economics & Reimbursement

    Edwards Lifesciences (Hartford, CT)
    …for Medicare Services (CMS) and/or Medicare Administrative Contractors (MAC), Medicaid, Veteran Affairs (VA) and commercial payers. **The Director , Global Health ... Maine, and New Hampshire** and will report to the Sr . Director East, Global Health Economics and...with various internal business partners (especially Sales, Marketing, Clinical, Regulatory , Legal, and Government Affairs staff) to… more
    Edwards Lifesciences (04/25/24)
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  • MSL Regional Director , GI - Non-Alliance…

    Sanofi Group (Hartford, CT)
    …lives of patients. **Job Description:** This position reports to the US Sr . Field Medical Director , Immunology (Non-Alliance). **Main Job Responsibilities:** + ... Immunology team which is a segment of the Medical Affairs Specialty Care organization. Our Medical Affairs ...serves as a valued strategic partner with Clinical, Commercial, Regulatory , and Market Access on therapeutic solutions to support… more
    Sanofi Group (05/13/24)
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  • Senior Program Manager, Strategic Project…

    Eversource Energy (Hartford, CT)
    …and budgets in the conceptual phase prior to execution + Interacts regularly with Regulatory Affairs , Environmental Affairs , and Energy Efficiency to develop ... first three months in the office\. Eversource is looking for a ** Senior Program Manager, Strategic Project Development, Transmission** located in **Hartford, CT** or… more
    Eversource Energy (05/01/24)
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  • Senior Program Manager, Strategic Project…

    Eversource Energy (Hartford, CT)
    …and budgets in the conceptual phase prior to execution + Interacts regularly with Regulatory Affairs , Environmental Affairs , and Energy Efficiency to develop ... **Our Team** Eversource is looking for a ** Senior Program Manager, Strategic Project Development** located in **Hartford, CT** or **Westwood, MA** or **Hooksett,… more
    Eversource Energy (03/06/24)
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  • Associate Clinical Research Associate - Central…

    Merck (Hartford, CT)
    …partnership with GCTO (Global Clinical Trial Operations) country operations, finance, regulatory affairs , pharmacovigilance, legal and regional operations, HQ ... **Job Description** With support of Sr CRA/CRA Clinical Research Associate) and/or CRA Manager,...a timely manner. + Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study… more
    Merck (05/18/24)
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