• Clinical Study Physician

    Teva Pharmaceuticals (Parsippany, NJ)
    …Physician Date: Nov 4, 2025 Location: Parsippany, United States, New Jersey, 07054 Company : Teva Pharmaceuticals Job Id: 63959 **Who we are** Together, we're on a ... safety signals. + Review documents supporting clinical development such as Investigator 's brochure, regulatory documents for IND/CTA, clinical sections of integrated… more
    Teva Pharmaceuticals (10/07/25)
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  • Associate Director, PV Sciences

    Taiho Oncology (Princeton, NJ)
    …safety reporting training. + Participate in the review of protocols, informed consents, Company Core Data Sheets, + Investigator Brochures, clinical summary of ... offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary… more
    Taiho Oncology (11/04/25)
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  • Sr Medical Science Liaison

    Terumo Medical Corporation (Somerset, NJ)
    …Date: Oct 30, 2025 Req ID: 5155 Location: Somerset, NJ, US, 08873 Company : Terumo Medical Corporation Department: Scientific Data & Communication **Job Summary** The ... + Build relationships and demonstrate the clinical outcome and benefits of company products to Key Opinion Leaders (KOL), medical groups and health systems.… more
    Terumo Medical Corporation (10/01/25)
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  • Sr. Study Manager, Clinical Operations

    Taiho Oncology (Princeton, NJ)
    …and issues. + Oversee systems to track projects including all study, investigator and ethical review board information, patient recruitment activity, and financial ... specific requirements and industry standards. + Verify that the investigator follows the approved protocol, training and all GCP...employee will be in an "at-will position" and the Company reserves the right to modify base salary (as… more
    Taiho Oncology (11/13/25)
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  • Director, Clinical Pharmacology Lead

    Organon & Co. (Jersey City, NJ)
    …2.5 and labeling for regulatory submissions, contribute the authoring of Investigator Brochures, IND subsections, briefing books, submission modules, responses to ... pharmacology components of TMED study protocols, clinical study reports, Investigator Brochures, briefing books, IND subsections, submission modules and other… more
    Organon & Co. (11/25/25)
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  • Director, SM Medical Affairs, Specimen Acquisition…

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …under development by the BU. + Reviews proposals for IIS ( Investigator -Initiated Studies) and Collaborative Studies. + Reviews advertising, educational, promotional ... for group For certain roles at BD, employment is contingent upon the Company 's receipt of sufficient proof that you are fully vaccinated against COVID-19. In… more
    BD (Becton, Dickinson and Company) (09/20/25)
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  • Senior Specialist, Clinical Quality Assurance…

    Merck (Trenton, NJ)
    …marketing, to ensure high-quality, safe, and effective products, contributing to the company mission of improving and saving lives around the world. Our Research ... Division QA Clinical Quality (CQ) provide independent assurance that our Company ensures the safety, rights, and well-being of participants, while complying… more
    Merck (11/19/25)
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  • Senior Medical Science Liaison - Biopharma…

    Sumitomo Pharma (Jersey City, NJ)
    Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... in the collection and exchange of scientific/technical information important to the Company 's market and development portfolio. + Assist in the management of… more
    Sumitomo Pharma (10/22/25)
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  • Associate Director, Clinical Science

    Bristol Myers Squibb (Princeton, NJ)
    …prepares study protocols, amendments, specific sections of study manuals and Investigator meeting materials, and other documents as needed with appropriate guidance ... the preparation/review of INDs, regulatory documents, IND annual report/DSURs, Investigator Brochures, and NDAs/MAAs. + Supports priorities within functional area.… more
    Bristol Myers Squibb (11/22/25)
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  • Manager, Evidence Generation, IME & Sponsorship…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …generation of medical evidence, (eg, observational studies, registries, and investigator -initiated studies (IISs) / investigator -initiated trials (IITs)) + Manage ... in evidence generation and communication/publications teams with a pharmaceutical or biotech company , CRO, academic research, or HEOR group + Prior experience in… more
    Otsuka America Pharmaceutical Inc. (11/14/25)
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