• Merck & Co. (Rahway, NJ)
    …within Fair Market Value based upon protocol design, industry benchmark data and clinical trial team feedback.Represent Global Site Budgets and Payments on ... dedicated colleagues while developing and expanding your career.The Senior Trial Initiation Specialist in Global Site Budgets...Clinical Trial Teams during trial ...Clinical Trial Teams during trial initiation as the… more
    HireLifeScience (06/08/24)
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  • 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 (06/08/24)
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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 Trials Specialist

    Actalent (Basking Ridge, NJ)
    …! This company has great culture and is rapidly growing! Summary: The Clinical Trial Specialist /In-house CRA provides technical and administrative support ... IMMEDIATE CLINICAL TRIALS SPECIALIST OPPORTUNITY WITH LEADING...to the clinical study team(s) responsible for clinical trial execution. This person may be… more
    Actalent (06/08/24)
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  • Senior Trial Initiation Specialist

    Merck (Rahway, NJ)
    …within Fair Market Value based upon protocol design, industry benchmark data and clinical trial team feedback. + Represent Global Site Budgets and Payments ... colleagues while developing and expanding your career. **The Senior Trial Initiation Specialist in Global Site Budgets...on Clinical Trial Teams during trial ...on Clinical Trial Teams during trial initiation as the… more
    Merck (06/08/24)
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  • Director, Clinical Scientist - Imaging…

    J&J Family of Companies (New Brunswick, NJ)
    Director, Clinical Scientist - Imaging Specialist (INTO) - 2406193420W **Description** At Johnson & Johnson, we believe health is everything. Our strength in ... opportunity to join Johnson & Johnson as a Director, Clinical Scientist- Imaging Specialist in our ...INTO clinical studies. Responsibilities include collaboration with clinical and cross function trial teams, external… more
    J&J Family of Companies (06/08/24)
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  • Clinical Trials Specialist

    Actalent (Basking Ridge, NJ)
    …or deviations from monitoring plan + Monitors and updates investigator/site status for the trial , and supports with clinical trial registry postings + ... Description: + Clinical Study Specialist supports Clinical...reference materials (eg, regulatory, pharmacy, and laboratory binders + Trial Master File reconciliations; manages and maintains the eTMF,… more
    Actalent (06/10/24)
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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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  • Senior Retention Specialist

    System One (Plainsboro, NJ)
    …quality, performance, regulatory compliance, and patient safety related to managing assigned clinical trial sites and document handling. + Attends and ... the main goal. They are seeking a Senior Retention Specialist to support patients enrolled in the clinical... trials. + A minimum of 5 years of clinical trial experience within a pharmaceutical, biotechnology,… more
    System One (05/13/24)
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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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  • 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 (New Brunswick, 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 (03/21/24)
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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 (Morristown, NJ)
    …for ensuring research charges are posted in accordance with Medicare's Clinical Trial Policy, federal regulations, and pharmaceutical/third party contracts. ... Description: The Research Compliance Specialist reviews, adjusts, and reports on clinical trials charges and claims representing research while working closely… more
    Actalent (06/08/24)
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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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