• Clinical Research Coordinator A

    University of Pennsylvania (Philadelphia, PA)
    …biological samples and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and ... and resources, and much more. Posted Job Title Clinical Research Coordinator A Job Profile Title Clinical...of a team, as well as independently; knowledge of IRB and human research protection… more
    University of Pennsylvania (07/24/25)
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  • Clinical Research Coordinator

    University of Pennsylvania (Philadelphia, PA)
    …biological samples and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and ... wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator A (Department of Endocrinology,Diabetes and Metabolism) Job… more
    University of Pennsylvania (08/09/25)
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  • Clinical Research Coordinator B

    University of Pennsylvania (Philadelphia, PA)
    …of CRO; adhere to all PENN, ICF, and FDA guidelines; prepare and process all IRB documentation. The clinical research coordinator B will also manage clinical ... PENN, ICF, and FDA guidelines; prepare and process all IRB documentation. The clinical research coordinator...as part of a team or independently. Knowledge of IRB and human research protection… more
    University of Pennsylvania (08/19/25)
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  • Clinical Research Coordinator A/B

    University of Pennsylvania (Philadelphia, PA)
    …adults and experience with administering cognitive assessments strongly preferred. Familiarity with IRB guidelines, human subject research practices, and ... and resources, and much more. Posted Job Title Clinical Research Coordinator A/B Job Profile Title Clinical...Assisting or leading in the preparation and submission of IRB documents Coordinator A: Assist in the… more
    University of Pennsylvania (08/08/25)
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  • Clinical Research Coordinator B/C

    University of Pennsylvania (Philadelphia, PA)
    …and expertise in GCP and institutional policies is expected. QUALIFICATIONS: Clinical Research Coordinator B + Bachelor's degree and 2-3 years of related ... and resources, and much more. Posted Job Title Clinical Research Coordinator B/C Job Profile Title Clinical...detail-oriented, and able to multitask effectively + Familiarity with IRB processes and human subject research more
    University of Pennsylvania (08/19/25)
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  • Research Coordinator - Clinical…

    Guthrie (Sayre, PA)
    …total research department. Other Duties: + Collaborate with executive director, manager, research team members and IRB coordinator in developing and ... research standards training preferred. The completion of the CITI Basic Research course regarding Human Subjects Protection Training is required within one… more
    Guthrie (08/22/25)
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  • Clinical Research Coordinator A/B

    University of Pennsylvania (Philadelphia, PA)
    …oriented and have prior experience with IRB guidelines and policies and human subject research practices and appropriate professional skills in the execution ... and resources, and much more. Posted Job Title Clinical Research Coordinator A/B Job Profile Title Clinical...is responsible for oversight, execution, and regulatory compliance of human subject research carried out in the… more
    University of Pennsylvania (06/10/25)
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  • Research Coordinator - Heart…

    WellSpan Health (York, PA)
    …protection of the safety and welfare of human subjects (ie, DHHS, FDA and IRB research regulations, HIPAA privacy and research regulations and others as ... **Common Expectations:** + Is knowledgeable of and complies with institutional research policies, procedures and guidelines. With...+ Heartsaver CPR/AED Upon Hire Required + Certified Clinical Research Coordinator Upon Hire Preferred or +… more
    WellSpan Health (07/22/25)
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  • Clinical Research Coordinator B/C

    University of Pennsylvania (Philadelphia, PA)
    …training and education to PPMC inpatient/cath lab cardiology nurses. + Support and train new research coordinator . + Review all new trials in the cath lab ... and resources, and much more. Posted Job Title Clinical Research Coordinator B/C Job Profile Title Clinical...according to regulatory requirements. + Prepares all documents for IRB review including draft informed consents written… more
    University of Pennsylvania (08/15/25)
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  • Clinical Research Coordinator A/B

    University of Pennsylvania (Philadelphia, PA)
    …ability to work as part of a team, as well as independently; knowledge of IRB and human research protection regulations; high reliable and good work ... and resources, and much more. Posted Job Title Clinical Research Coordinator A/B Job Profile Title Clinical...or CRO, includes source documentation, case report forms, and research charts. Collect, review and report study… more
    University of Pennsylvania (08/22/25)
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