• Regulatory Compliance Specialist - Medicine…

    Houston Methodist (Houston, TX)
    …Harmonization (ICH). This position will work closely with the study teams for study start - up regulatory paperwork, maintain regulatory documents such as ... At Houston Methodist, the Regulatory Compliance Specialist position is responsible for coordinating...position is responsible for coordinating and performing study specific regulatory processes such as local IRB and external IRB… more
    Houston Methodist (04/06/25)
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  • Regulatory Analyst 2 - Remote

    University of Miami (Miami, FL)
    … Analyst II reviews, prepares, and provides oversight for initial and subsequent regulatory submissions from study start - up through study closure as ... well as the maintenance of regulatory documents to ensure compliance with applicable requirements and...the process of study submissions (initial and amendment) and regulatory document maintenance; serves as point of contact for… more
    University of Miami (04/02/25)
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  • Clinical Research Specialist

    University of Pennsylvania (Philadelphia, PA)
    …of the initiation of Phase I-V clinical trials with a focus on required regulatory start - up approvals and associated site initiation documentation. Reporting ... Summary Temporary Employee - Non-Exempt Job Description Ophthalmology seeks a part-time Regulatory Affairs Start - Up Specialist-CC to facilitate, with minimal… more
    University of Pennsylvania (05/04/25)
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  • Head of Feasibility

    Sanofi Group (Swiftwater, PA)
    …this role you will provide expert guidance on country and site selection strategies, regulatory considerations and start - up timelines, as well as patient ... and work to define the way of working and generating standardization among study start up team. + Recruitment and Screening: Assist with the creation and… more
    Sanofi Group (05/01/25)
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  • Associate Clinical Site Lead

    Abbott (Minneapolis, MN)
    …Site Contracts Associate), as needed. Manage all aspects of study lifecycle to include site regulatory and quality: + Start Up + Nominate, approach, and ... + Identify, develop, and maintain sites capable of delivering start - up goals, study participation levels and required...up process and site initiation visits + Understand regulatory and legal requirements for study participation at a… more
    Abbott (06/21/25)
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  • Clinical Site Lead

    Abbott (Houston, TX)
    …Contracts Associate), as needed. **Manage all aspects of study lifecycle to include site regulatory and quality:** + ** Start Up ** + Nominate, approach, and ... + Identify, develop, and maintain sites capable of delivering start - up goals, study participation levels and required...up process and site initiation visits + Understand regulatory and legal requirements for study participation at a… more
    Abbott (06/05/25)
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  • Director of Clinical Research Consulting

    Vitalief (New Brunswick, NJ)
    …(for Industry, NIH, Cooperative Group, NCI and Investigator Initiated sponsored trials); Regulatory work required for start - up documents; Processes related ... work for Industry, NIH, Cooperative Group, NCI and Investigator Initiated sponsored trials; Regulatory work for start - up document; Contract review and… more
    Vitalief (05/01/25)
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  • Regulatory Analyst 3

    University of Miami (Miami, FL)
    …and/or Director of Regulatory with the day-to-day operations related to study start - up activities and regulatory maintenance of study records. CORE JOB ... SCCC has an exciting opportunity for a Full Time Regulatory Analyst 3 to work at the UHealth Medical...federal regulations. This process will take place from study start - up throughout the completion of the study.… more
    University of Miami (04/26/25)
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  • Clinical Research Coordinator A

    University of Pennsylvania (Philadelphia, PA)
    …platform. Responsibilities include preparing and processing regulatory documents to all regulatory committees from study start up to study completion. ... include preparing and processing regulatory documents to all regulatory committees from study start up to study completion. Interacting with study… more
    University of Pennsylvania (06/25/25)
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  • Clinical Program Manager (RN/NP Required) - Tisch…

    Mount Sinai Health System (New York, NY)
    …Staff regarding specific protocols. + Manage clinical trials portfolio and assure timely regulatory start - up of protocols. + Monitor accruals and identify ... study enrollment, establishing a database of patients, protocol treatment and follow- up care for patients participating in clinical trials. + Collaborates with… more
    Mount Sinai Health System (06/25/25)
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