• Eisai, Inc (Nutley, NJ)
    …is your profile, we want to hear from you. The Associate Medical Director , US Neurology Medical Affairs will provide medical leadership for medical ... Management, Territory Management (MSL)Eisai Salary Transparency Language:The base salary range for the Associate Medical Director , US Medical Affairs is from… more
    HireLifeScience (07/23/25)
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  • Eisai, Inc (Nutley, NJ)
    …a difference. If this is your profile, we want to hear from you. The Associate Director (AD), Global Medical Affairs Training and Education is responsible ... & International). Eisai Salary Transparency Language:The base salary range for the Associate Director , Global Medical Affairs Training and Education… more
    HireLifeScience (06/28/25)
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  • Merck & Co. (Rahway, NJ)
    …as required, and recognized scientific expertiseExtensive experience in medical affairs or clinical developmentStrong prioritization and decision-making skills ... Job DescriptionThe Executive Director Pulmonary Hypertension, Value & Implementation (V&I), Global...Skills: At least 5 years global or US medical affairs or clinical development experience with proven… more
    HireLifeScience (07/17/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …working with contract manufacturing organizations CMO. This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub team and the RA ... technical teams in preparation of submission documents to include clinical trial applications/amendments (eg, IND, IMPD, IB) and marketing applications/supplements… more
    HireLifeScience (05/15/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …of a CDx study/IVDR performance evaluation study integration of an assay into clinical testing (before testing) and once data is ready for CDx submission (after ... to external diagnostic business partners specifically:Use of CTA/CDx within clinical trialsDevice protocols and SAPsDevice non-significant/significant risk determinations (both… more
    HireLifeScience (05/29/25)
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  • Merck & Co. (Rahway, NJ)
    …in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects; and assist the Executive Director and/or ... medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will... development (pre- clinical to post-licensure). The Senior Director will manage the entire cycle of late-stage … more
    HireLifeScience (07/25/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionRole SummaryUnder the guidance of a senior leader, an Associate Principal Scientist/ Associate Director , has primary responsibility for ... HTA submissions. The incumbent is expected to work cross-functionally with clinical development, medical affairs , biostatistics, market access, commercial and… more
    HireLifeScience (07/23/25)
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  • Merck & Co. (North Wales, PA)
    Job DescriptionRole SummaryThe Associate Director , Global Scientific & Value Content-Healthcare Professional (AD, GSVC-HCP), position resides in the Value & ... Implementation (V&I) organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research.This mid-level, headquarters-based position… more
    HireLifeScience (07/15/25)
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  • Eisai, Inc (Nutley, NJ)
    …make a difference. If this is your profile, we want to hear from you. Associate Director , Medical Education - Oncology, is responsible for the strategic planning ... & ManagementEisai Salary Transparency Language:The base salary range for the Associate Director , Medical Education - Oncology is from :162,600-213,400Under… more
    HireLifeScience (06/28/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …Sankyo. The candidate will collaborate globally with Formulation and Analytical Scientists, Clinical Operations, Regulatory Affairs CMC, and Clinical ... to author the Dose Preparation Instructions and address questions from the clinical sites. The candidate will optimize and continuously improve the Pharmacy Manual… more
    HireLifeScience (05/18/25)
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  • Genmab (NJ)
    …love to have you join us!The Global Regulatory Labeling, Policy and Intelligence Associate Director will primarily be responsible for leading the development and ... be within Global Regulatory Affairs (GRA) and will report to the Sr. Director , Labeling, Policy and Intelligence. The position may be based in our Princeton, New… more
    HireLifeScience (07/09/25)
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  • Insmed Incorporated (Los Angeles, CA)
    …for Women™, Best Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Associate Director Medical Science Liaison will develop and maintain ... insights to Insmed.Support research and development programs as requested by R&D, Clinical Operations, and Medical Affairs Departments. This may include trial… more
    HireLifeScience (06/20/25)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …design pull you in? Are you ready to experiment with us? The Position The Associate Director of Nephrology Key Opinion Leader Marketing will be a pivotal driver ... with brand/therapy area vision and message. Relationships Reports to Senior Director of Cardio Renal Marketing Responsible for providing interface with key… more
    HireLifeScience (06/28/25)
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  • Mirum Pharmaceuticals (San Mateo, CA)
    …care, be real, get it done, and have fun, seriously. POSITION SUMMARY The Associate Director , Global Regulatory Affairs provides management of all aspects ... development and commercialization of novel liver drugs including quality, preclinical and clinical areas of drug development. This position will manage the timely… more
    Upward (07/19/25)
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  • Bristol-Myers Squibb Company (Princeton, NJ)
    …work and in their personal lives. Read more: careers.bms.com/working-with-us. The Associate Director , WW Medical Cell Therapy Autoimmune, LCM/Pan-Indication, ... in the disease area within the pharmaceutical industry, such as within Medical Affairs or Clinical Development Strong interpersonal and communication skills to… more
    Upward (07/24/25)
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  • Acadia Pharmaceuticals Inc. (Princeton, NJ)
    …work in our office three days per week on average. Position Summary The Associate Director , Regulatory CMC, is responsible for contributing to/assisting with the ... States and Canada for the treatment of Rett syndrome. Our clinical -stage development efforts are focused on Prader-Willi syndrome, Alzheimer's disease psychosis,… more
    Upward (07/07/25)
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  • AbbVie (North Chicago, IL)
    …compliance, and contributes to the overall success of drug/device development programs. Associate Director , Safety, Medical & Regulatory Quality is part of ... dynamic. Emphasizing and embedding quality in the execution of clinical trials, post market vigilance and post market studies,...the R&D Quality Medical Affairs (MA) QA team which provides independent quality oversight… more
    Upward (07/19/25)
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  • eGenesis (Cambridge, MA)
    …in genome editing. POSITION SUMMARY eGenesis is seeking a highly motivated and experienced Associate Director of Clinical Science to join our Clinical ... in all clinical programs Work with internal stakeholders including Clinical Development, Regulatory Affairs , Non- Clinical , and Translational teams… more
    Upward (07/19/25)
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  • Takeda Pharmaceutical Company Limited (Lexington, MA)
    …my employment application is true to the best of my knowledge. Job Description Associate Director , Clinical Research, Value & Evidence Generation, US Medical ... and leadership to ensure successful operational execution of all US Medical Clinical Research including, Medical Affairs Company Sponsored Studies (MACS)… more
    Upward (07/07/25)
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  • Corcept Therapeutics (Redwood City, CA)
    …a fundamental shift in the way we understand and treat disease. The Associate Director , Scientific Publications, will provide expert scientific and medical ... support, focusing on publication strategy and execution for Oncology Medical Affairs -led publications in tandem with Clinical Development-led publication… more
    Upward (07/19/25)
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