• Site Deviation Investigator

    Catalent Pharma Solutions (Greendale, IN)
    ** Site Deviation Investigator ** **Position Summary** + **Work Schedule:** Monday to Friday, business hours + 100% on- site in Greendale, IN Greendale is ... nutraceuticals via confection to enhance wellness for all consumers. The ** Site Deviation Investigator ** will be independently responsible for the efficient… more
    Catalent Pharma Solutions (11/12/25)
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  • QC Analytical Investigator

    Insight Global (Boston, MA)
    Job Description Insight Global is looking for a QC Analytical Investigator to sit on- site at a brand new facility in the beautiful Seaport district of Boston ... one of our top pharmaceutical clients. This is a first shift role, on- site Monday through Friday. This position will be supporting the growing technical services… more
    Insight Global (09/09/25)
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  • Senior Specialist, Clinical Quality Assurance…

    Merck (Annapolis, MD)
    …and perform risked-based audits + Activities may include GCP audits of investigator sites, suppliers, third party collaborations and due diligence activities. + In ... escalation of quality issues, including potential misconduct or issues of significant deviation with projects/products, to the QAL and TA Head. + Interfaces and… more
    Merck (11/19/25)
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  • Intermittent/PRN Senior Research Nurse, CTRU…

    Ohio University (Athens, OH)
    …studies include both sponsored clinical trials (Phases I-IV) and investigator -initiated research studies (qualitative and quantitative) conducted through the Ohio ... ) for review and approval (ie initial, continuing review, deviation , AE/ SAE , close-out, etc.) + May assist...May assist with research project budget development + Ensuring site compliance with all research protocols and regulatory requirements… more
    Ohio University (09/02/25)
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  • Clinical Research Coordinator A/B

    University of Pennsylvania (Philadelphia, PA)
    …proposals, and research related presentations. Works closely with the Principal Investigator , manager, and study team to identify problems and develop solutions. ... needed and monitor results. Responsible for study coordination for investigator -initiated studies, multi-center research studies, and patient-oriented clinical and… more
    University of Pennsylvania (10/03/25)
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  • Medical Director/Clinical Trial Physician…

    ThermoFisher Scientific (Suwanee, GA)
    …to the study executive and independent safety committee if applicable; medical training of site staff at Investigator meetings; CRA training in new indications + ... clinical trial protocols while implementing the latest scientific information, contribute to site selection, contribute to review and approval of study protocols and… more
    ThermoFisher Scientific (11/12/25)
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  • Clinical Research Coordinator 1

    University of Miami (Miami, FL)
    …Monitors, Clinical research Coordinators and PIs in the organization and preparation of Site Initiation Visits (SIV). Attend site disease group tumor board ... and as required per UM policy. Under the supervision of the Principal Investigator . Determine data to be collected and develop forms for collecting/summarizing data.… more
    University of Miami (10/22/25)
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  • Clinical Research Coordinator 2

    University of Miami (Miami, FL)
    …standards and clinical credentials as delegated by the Principal Investigator . 6. Monitors, documents, reports, and follows-up on study unanticipated/adverse ... in implementing protocol amendments under direct supervision of the Principal Investigator . 8. Assists with study orientation and protocol related in-services to… more
    University of Miami (10/21/25)
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  • Sr. Operation Associate - Warehouse

    Lilly (Concord, NC)
    …area deviation and corrective action discussions as a lead investigator with a cross-functional team from Engineering, Maintenance, Technical Services / ... reliable supply of products to patients. + Lead the deviation process for the warehouse operations in collaboration with...Understand and influence the Material control strategy for the site . + Provide operational and project support for the… more
    Lilly (11/05/25)
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  • Clinical Research Coordinator

    IQVIA (Troy, NY)
    …Description **Job Title:** Clinical Research Coordinator **Work Set-Up:** Working On- site **Schedule** : 16 hours per week. **Responsibilities:** + **Phlebotomy** ... signs.** + Coordinate clinical research studies conducted by a supervising principal investigator . + Update and maintain skills, training, and knowledge of current… more
    IQVIA (11/20/25)
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