• Merck & Co. (Rahway, NJ)
    …pharmacokinetic, exposure-response, quantitative system pharmacology, and other model-based analyses.-Perform clinical trial simulations to inform dose selection ... the-Quantitative Pharmacology and Pharmacometrics --Immune/Oncology-(QP2-IO)-team in the role of-Senior Specialist .--QP2-IO team is part of the Global Clinical more
    HireLifeScience (06/04/24)
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  • Clinical Trial Recruitment…

    Vitalief (Newark, NJ)
    …weekend work could be required. Responsibilities: + Reporting to a Clinical Trial Recruitment Team Lead, the Recruitment Specialist will work with the Team ... with Rutgers University and seeking several talented and enthusiastic Clinical Trial Recruitment Specialists to join our...areas that are underrepresented in research. As a recruitment specialist , you will play a vital part in these… more
    Vitalief (03/10/24)
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  • Clinical Trial Specialist

    Vitalief (New Brunswick, NJ)
    …Join us and help clients adapt to evolving requirements in the research and clinical trial industry with cutting-edge solutions. Reasons to Work for Vitalief: + ... patient recruiting/pre-screening/consenting/retention; activation; regulatory compliance, data management. and other clinical trial activities for solid tumor, high… more
    Vitalief (04/17/24)
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  • Clinical Research Specialist

    Rockefeller University (New York, NY)
    …and new investigator audits, tracks deviations for early intervention, and supports clinical trial registration in Good Clinical Practice (GCP) ... For more information,please see the hospital website at: http://www.rucares.org/ Overview The Clinical Research Specialist serves as a regulatory expert and… more
    Rockefeller University (05/29/24)
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  • Data Standards Specialist , Global…

    Merck (Rahway, NJ)
    …Data Tabulation Model (SDTM) + A broad comprehensive knowledge of the clinical trial process including data management (data collection, processing, storage, ... regulations + Ensuring the definitions are maintained and aligned across the clinical lifecycle (eg, data collection, analysis & report, and submission) deliverables… more
    Merck (06/06/24)
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  • Start Up Specialist - Oncology

    Hackensack Meridian Health (Hackensack, NJ)
    …**Start Up Specialist ** is responsible for the oversight and management of clinical trial start-up activities and serves as a primary contact for ... A day in the life of a **Start Up Specialist ** at Hackensack Meridian _Health_ includes: + Manages all...and Execution of Confidentiality Agreements, Material Transfer Agreements and Clinical Trial Agreements. + Independently oversees … more
    Hackensack Meridian Health (05/10/24)
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  • Senior Regulatory Specialist

    Hackensack Meridian Health (Hackensack, NJ)
    …**Senior Regulatory Specialist ** is responsible for the oversight and management of clinical trial regulatory for all assigned clinical trials and serves ... as ensuring ongoing compliance of study-related documentation throughout the clinical trial lifecycle for all assigned ...A day in the life of a **Senior Regulatory Specialist ** at **Hackensack Meridian** **_Health_** includes: + Assists with… more
    Hackensack Meridian Health (05/18/24)
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  • Start Up Specialist

    Actalent (Parsippany Troy Hills, NJ)
    …the Review and Execution of Confidentiality Agreements, Material Transfer Agreements and Clinical Trial Agreements. + Independently oversees Clinical ... Investigator (PI) by providing administrative support to develop, implement and complete clinical trial submissions. + Prepares clinical trial documents… more
    Actalent (05/29/24)
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  • Start Up Specialist

    Actalent (Hackensack, NJ)
    …the Review and Execution of Confidentiality Agreements, Material Transfer Agreements and Clinical Trial Agreements. Independently oversees Clinical Trial ... (PI) by providing administrative support to develop, implement and complete clinical trial submissions. Prepares clinical trial documents that… more
    Actalent (06/05/24)
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  • Research Billing Compliance Specialist

    Hackensack Meridian Health (Hackensack, NJ)
    …for ensuring research charges are posted in accordance with Medicare's Clinical Trial Policy, federal regulations and pharmaceutical/third party contracts. ... a leader of positive change. The **Research Billing Compliance Specialist ** reviews, adjusts, and reports on clinical ...PFS, registration and third parties to ensure adherence to clinical trial billing workflows. + Provides guidance… more
    Hackensack Meridian Health (06/06/24)
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  • Investigative Specialist 1 (Law)

    New York State Civil Service (Brooklyn, NY)
    NY HELP Yes Agency Attorney General, Office of the Title Investigative Specialist 1 (Law) Occupational Category No Preference Salary Grade 18 Bargaining Unit PS&T - ... child protective services investigator, in an investigative position involving trial preparations and detailed reports, or investigations within a branch… more
    New York State Civil Service (05/25/24)
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  • Therapy Development Specialist , CoreValve…

    Medtronic (Morristown, NJ)
    …RESPONSIBILITIES:** The following responsibilities are to be performed as appropriate in clinical trial case support and/or case support following commercial ... EKG, blood pressure, wave forms, and ancillary procedural solutions + Knowledge of Clinical trial protocols, and CoreValve and other Medtronic TAVR product IFUs… more
    Medtronic (03/30/24)
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  • Regulatory Specialist

    Hackensack Meridian Health (Hackensack, NJ)
    …audits, as well as ensuring ongoing compliance of study-related documentation throughout the clinical trial lifecycle for all assigned clinical trials. ... serve as a leader of positive change. The **Regulatory Specialist ** is responsible for ensuring compliance with Federal, State,...the Medicare Coverage Analysis, budget and contract for a clinical trial in order to initiate a… more
    Hackensack Meridian Health (05/21/24)
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  • Sr Clinical Research Associate…

    ThermoFisher Scientific (New York, NY)
    clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy ... FSO, FSP, Government, etc.). Acts as a site processes specialist , ensuring that the trial is conducted...study systems are updated per agreed study conventions (eg Clinical Trial Management System, CTMS). Performs QC… more
    ThermoFisher Scientific (05/02/24)
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  • Regional Leadless Specialist , CRM

    Abbott (New York, NY)
    …heart arrhythmias, or irregular heartbeats. **WHAT YOU'LL DO:** The Regional Leadless Specialist provides technical, clinical , educational and sales support to ... ensure adoption and growth of Abbott leadless technology. The Regional Leadless Specialist works closely with internal and external customers to drive therapy… more
    Abbott (06/03/24)
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  • Research Compliance Specialist

    Actalent (Hackensack, NJ)
    …for ensuring research charges are posted in accordance with Medicare's Clinical Trial Policy, federal regulations, and pharmaceutical/third party contracts. ... The Research Compliance Specialist reviews, adjusts, and reports on clinical trials charges and claims representing research while working closely with the… more
    Actalent (06/07/24)
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  • Senior Specialist - Quantitative…

    Merck (Rahway, NJ)
    …exposure-response, quantitative system pharmacology, and other model-based analyses. + Perform clinical trial simulations to inform dose selection and go/no-go ... -** **Immune/Oncology** **(QP2-IO)** team in the role of Senior Specialist . QP2-IO team is part of the Global ...Specialist . QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development… more
    Merck (06/04/24)
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  • Clinical Research Coordinator

    Hackensack Meridian Health (Nutley, NJ)
    …works under the general supervision of the principal investigator responsible for the clinical trial (s) to which is assigned. **Responsibilities** A day in the ... on each protocol and each patient participating in a clinical trial protocol in the clinical...+ Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist more
    Hackensack Meridian Health (05/22/24)
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  • Sr Clincial Specialist Coronary Renal…

    Medtronic (New York, NY)
    …stakeholders to determine appropriate clinical evaluation strategy; may provide input to clinical trial design + Identify potential evidence gaps or risks to ... and communicate risks as needed + Stay current on clinical evidence landscape and provide guidance to teams on...sufficient data + Develop and maintain in-depth knowledge of clinical evaluation best practices and regulatory agencies' guidelines on… more
    Medtronic (04/16/24)
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  • Site Readiness & Regulatory Specialist

    Actalent (New York, NY)
    …IRB/IEC and other applicable regulations/guidelines. Demonstrated basic understanding of the clinical trial process Education: Level of education preferred (if ... burn with the support of more senior specialists Skills: Contract, clinical research, contracts, negotiation, Regulatory Top Skills Details: Contract, clinical more
    Actalent (06/04/24)
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