• Clinical Research Director - RBD

    Sanofi Group (Morristown, NJ)
    regulatory , statistics, and PM) + The CRD will lead the preparation of clinical documents/reports for regulatory submission and will attend meetings with ... **Job Title:** Clinical Research Director - RBD **Location:** Cambridge, MA...collaboration with the Global Project Head (GPH) and Project Manager (PM), including the relevant components of the GCDP… more
    Sanofi Group (08/25/25)
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  • Senior Manager Statistical Programming

    Regeneron Pharmaceuticals (Warren, NJ)
    The Senior Manager Statistical Programming for Medical Affairs provides timely support to the Medical Affairs project team on all programming matters ... to regulatory approval, product launch, and annual reports. The Senior Manager Statistical Programming for Medical Affairs may serve as the statistical… more
    Regeneron Pharmaceuticals (07/31/25)
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  • Lead, Clinical Data Management - MedTech

    J&J Family of Companies (Raritan, NJ)
    …Rhode Island, Massachusetts, Vermont, New Hampshire, & Maine_ . **Purpose** : The Lead Clinical Data Manager will be responsible with leading all aspects of ... **You will be responsible for** : Reporting to the Manager , Clinical Data Management this individual will:...and written communication skills. + Knowledge of GCP and regulatory requirements regarding clinical data management documentation… more
    J&J Family of Companies (08/29/25)
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  • Senior/Patient Advocacy & Medical Society…

    United Therapeutics (Trenton, NJ)
    …Cross functional collaboration: Partner closely with internal teams such as: marketing, clinical development, medical affairs , public policy, and compliance to ... patient partnership + Enhance patient recruitment for research including clinical trials, medical affairs studies, HEOR studies,...clinical trials and studies + Serve as project manager over assigned areas Minimum Requirements Manager :… more
    United Therapeutics (08/23/25)
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  • Sr. Manager , Supply Chain

    Mitsubishi Chemical Group (Jersey City, NJ)
    …by closely working with MTP internal colleagues in various functions (Quality Assurance, Regulatory Affairs , Marketing, Market Access, Medical Affairs , Drug ... effectively with colleagues in Supply Chain, Accounting, Market Access, Quality Assurance, Regulatory Affairs , Finance, etc. of Mitsubishi Tanabe Pharma Group,… more
    Mitsubishi Chemical Group (06/13/25)
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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 ... goals are met and addressed. + The Risk Safety Manager will work in conjunction with the Clinical... Manager will work in conjunction with the Clinical Quality/Safety Department towards the development and implementation of… more
    Virtua Health (08/08/25)
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  • Manager , Medical Information Scientific…

    J&J Family of Companies (Titusville, NJ)
    …after-hours phone coverage for emergency escalations on a rotating basis. The Manager , MISE will conduct training sessions for clinical skill ... for humanity. Learn more at https://www.jnj.com **Job Function:** Medical Affairs Group **Job Sub** **Function:** Medical Writing **Job Category:** Professional… more
    J&J Family of Companies (08/26/25)
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  • Manager Brand Marketing

    Nestle (Bridgewater, NJ)
    …and clinical proof + **Partner Cross-Functionally:** Collaborate closely with Regulatory , Sales, R&D, and Medical Affairs to ensure compliant, impactful ... and analytical acumen, with creative storytelling instincts + Comfort navigating clinical data, regulatory considerations, and emotional narratives **SKILLS:** +… more
    Nestle (08/08/25)
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  • Manager , R&D Paralegal

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …The ideal candidate will have a strong background negotiating agreements related to pre- clinical and clinical research (international experience a plus) in the ... and will provide legal support and assistance for various R&D and regulatory -related activities. This role requires frequent interaction with leadership and other… more
    Otsuka America Pharmaceutical Inc. (08/08/25)
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  • Manager , PVRM

    Sumitomo Pharma (Trenton, NJ)
    …but not limited to, Clinical Development, Translational Medicine/Early Development, Regulatory Affairs , Data Management and Biostatistics is essential. **Job ... as required. + Coordinate responses to ad hoc safety issues such as regulatory authority, site, or health care professional requests, along with PV physician,… more
    Sumitomo Pharma (08/01/25)
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