• Research Services Professional (Regulatory…

    University of Colorado (Aurora, CO)
    …and sponsor guidelines** **Examples of Duties Performed** **Regulatory- 40%** + Submit clinical trial protocols with applicable essential documents to our local ... research teams to plan, coordinate, and support research proposal submissions. + Track and monitor ...Clinical and Other- 10%** + Occasionally serve as clinical trial coordinator back-up, including assisting with… more
    University of Colorado (08/10/25)
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  • Post-Approval Compliance Monitor

    Alaka'ina Foundation Family of Companies (Silver Spring, MD)
    …best practices REQUIRED SKILLS AND EXPERIENCE: + Minimum three (3) years experience as a Clinical Trial Monitor + Knowledge and experience in the areas of ... Post-Approval Compliance Monitor Location MD - Silver Spring Job Code...provide training, as needed/requested. DESCRIPTION OF RESPONSIBILITIES: The WRAIR-based clinical research scientific monitoring services (Post-Approval Compliance… more
    Alaka'ina Foundation Family of Companies (09/19/25)
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  • Research Administrator

    University of Southern California (Los Angeles, CA)
    …projects, including contracts, grants, clinical trials, and philanthropic funding. + Clinical Trial Administration: Manage financial aspects of clinical ... Research Administratorto support our growing and dynamic research department. Reporting to the Senior Clinical ...fast-paced academic environment + 5+ years of experience in clinical trial financial management + Experience with… more
    University of Southern California (09/25/25)
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  • Senior Clinical Scientist, Late Development…

    Bristol Myers Squibb (Madison, NJ)
    …implementation all study startup/conduct/close-out activities as applicable + Evaluate innovative trial designs (collaboration with Medical Monitor / Clinical ... + Responsible for implementation, planning, and execution of assigned clinical trial activities. Serves as Clinical...preferred) **Experience Requirements** + 5+ years of experience in clinical science, clinical research , or… more
    Bristol Myers Squibb (09/21/25)
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  • Oncology Research Coordinator

    Penn Medicine (West Chester, PA)
    …education updates to all investigators and CCH staff that have eligible participants for clinical research trials as needed. Acts as a resource for the treating ... group and/or industry sponsored studies required. Proficient in regulatory component of clinical research . Computer literacy required and proficient in Excel… more
    Penn Medicine (09/30/25)
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  • Registered Nurse (RN), HVC Research

    Dartmouth Health (Lebanon, NH)
    …with research and non- research staff, maintaining involvement throughout the clinical trial process. The role of the Clinical Research ... Overview The Clinical Research Nurse I performs a...families, they provide care, education and support throughout the trial . Under the supervision of the PI or their… more
    Dartmouth Health (07/21/25)
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  • Sr. Research Program Coordinator II…

    Johns Hopkins University (Baltimore, MD)
    …for lower level program coordinators working at other locations within multi-centered clinical trial . + Develop standard operating procedures for regulatory ... term follow up at 28 and/or 90 days. Each trial is a little different depending on the intervention...Good Clinical Practice, ICH Guidelines, and SKCCC Clinical Research Office policies. Teaches staff about… more
    Johns Hopkins University (09/13/25)
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  • Senior Oncology Clinical Development…

    Astellas Pharma (Northbrook, IL)
    …Documented experience planning and managing clinical trials, serving as medical monitor , managing trial execution in coordination with clinical ... with the Clinical development Plan. Accountable for Clinical trial scope development and authoring of...thoracic oncology or immuno-oncology in solid tumors + Prior clinical research experience in an academic setting… more
    Astellas Pharma (08/08/25)
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  • Clinical Safety Specialist

    J&J Family of Companies (Danvers, MA)
    …executing clinical trial safety activities and responsibilities for the clinical research programs. **You will be responsible for:** + **Management of ... safety related clinical trial activities for assigned studies including:**...Minimum of 5 years' experience implementing safety processes or clinical research experience including management of safety… more
    J&J Family of Companies (10/08/25)
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  • Senior Manager, Clinical Operations

    ConvaTec (Lexington, MA)
    …+ Working closely with Clinical Study Managers (CSMs) and Clinical Research Associates (CRAs), manage all operational aspects from start-up ... activities. + Support the selection, oversight, and management of Clinical Research Organizations (CROs) and other vendors...leaders and clinical site staff to support clinical trial enrolment and other activities. +… more
    ConvaTec (09/19/25)
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