• Clinical Document Specialist (Hybrid)

    RWJBarnabas Health (New Brunswick, NJ)
    …and software Preferred: + CCDS certification (preferred) + Prior experience in clinical documentation review + Understanding of ICD-10-CM coding requirements + ... Clinical Document Specialist (Hybrid)Req #:0000175148 Category:Clerical / Administrative...Working Hours: Hybrid - four days onsite, one day remote + Physical Working Location: RWJUH - New Brunswick,… more
    RWJBarnabas Health (08/28/25)
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  • Senior Clinical Scientist - Ophthalmology

    Merck (Rahway, NJ)
    …the clinical trial team. + Leading medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaborations with ... in collaboration with Data Management/Programming. + Collaborating cross-functionally to monitor clinical data to ensure quality , completeness, and integrity of… more
    Merck (09/05/25)
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  • Clinical Development Program Lead,…

    Bristol Myers Squibb (Madison, NJ)
    …+ The role includes support of across portfolio activities in line with Clinical Excellence, including eg Protocol Review Committee, support of Business ... their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Clinical Development Program Leader sits within Clinical Development,… more
    Bristol Myers Squibb (08/30/25)
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  • Sr. Medical Director, Clinical Development…

    Bristol Myers Squibb (Princeton, NJ)
    …tumors, with a focus on GU cancers. This role provides medical direction and high quality scientific and clinical knowledge to lead the strategy and execution of ... implement clinical studies + Contribute to writing of protocols, investigator brochures, clinical study reports, and review of other clinical trial and… more
    Bristol Myers Squibb (07/08/25)
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  • HCC Risk Adjustment Auditor - Full Time…

    Datavant (Trenton, NJ)
    …in weekly coding project review meetings + Any other tasks asked by quality supervisor **What You Need to Succeed:** + 2 years' HCC Coding experience + 2 ... As an HCC (Hierarchical Condition Category) Auditor you will review medical records that have been coded in a...purposes. You will play a critical role in translating clinical documentation into precise codes that reflect the complexity… more
    Datavant (08/01/25)
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  • Director, Program Operations Leader - Early Phase…

    Regeneron Pharmaceuticals (Warren, NJ)
    …in Clinical Trial Management (CTM). This individual is responsible for clinical operations activities and decisions including quality , timelines and budgets ... communicates progress, risks, issues or changes that may impact quality , timelines and/or budget; provide clinical program... program(s) * Provide input and operational insight into Clinical Study Concepts (CSC) * Review of… more
    Regeneron Pharmaceuticals (08/19/25)
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  • Senior Managed Care Analyst (Hybrid/ Remote

    RWJBarnabas Health (Oceanport, NJ)
    Senior Managed Care Analyst (Hybrid/ Remote ) - Oceanport, NJReq #:0000205920 Category:Professional / Management Status:Full-Time Shift:Day Facility:RWJBarnabas Health ... negotiations, rate modeling, payer relationship management and contract performance review . Additionally, the position will collaborate with all departments of… more
    RWJBarnabas Health (06/26/25)
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  • Program Analyst - Remote

    Prime Therapeutics (Trenton, NJ)
    …drives every decision we make. **Job Posting Title** Program Analyst - Remote **Job Description** The Program Analyst is responsible for providing project ... support to one or more of Prime's functional areas: Clinical Program Management, Utilization Management (UM), Formulary, GuidedHealth, Pharmaceutical Trade… more
    Prime Therapeutics (09/03/25)
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  • HCC Risk Adjustment Coder - Full Time…

    Datavant (Trenton, NJ)
    …vision for healthcare. As an HCC (Hierarchical Condition Category) coder you will review medical records to identify and code diagnoses using a standardized system, ... purposes. You will play a critical role in translating clinical documentation into precise codes that reflect the complexity...severity of a patient's health status. **You will:** + Review , analyze, and code diagnostic information in a patient's… more
    Datavant (08/26/25)
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  • Associate Director, Oncology Clinical

    Bristol Myers Squibb (Princeton, NJ)
    …development process; including experience with implementing a biomarker strategy + Clinical protocol authoring and review of regulatory documents. + ... biology, mechanism of action, and predictive biomarkers in our late-stage clinical oncology portfolio. Ideal candidates will possess a strong scientific background,… more
    Bristol Myers Squibb (09/05/25)
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