- 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 ... assessments at each visit are performed, reporting adverse events and ensuring review and appropriate follow-up by investigator. + Prepare detailed documentation of… more
- 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 ... + Adhere to all University of Pennsylvania, informed consent form (ICF), and IRB guidelines. Position is contingent upon funding. QUALIFICATIONS: BA/BS and 1-2 year… more
- University of Pennsylvania (Philadelphia, PA)
- …sites and assists in the management of multisite trials. Job Description Prepare and process all Institutional Review Board ( IRB )through the IRB and ... other regulatory groups as appropriate including initial submissions, amendments, continuing reviews, adverse events and serious adverse events . Coordinate, organize and maintain all documentation required by sponsor or CRO (case report forms, source… more
- System One (Pittsburgh, PA)
- …with study participants and potential community recruits. + Assists with and adheres to Institutional Review Board ( IRB ) renewal, modification, and ... approved protocols. + Recruits research subjects and conducts interviews and research assessments. Requirements: + Minimum Education Requirement: Bachelor's Degree + Experience Requirement: At least 3-5 years of clinical trial/clinical research experience… more
- System One (Pittsburgh, PA)
- …and monitoring patients for complications and outcomes. + Assists with and adheres to Institutional Review Board ( IRB ) renewal, modification, and ... approved protocols. Recruits research subjects and conducts interviews and research assessments. Requirements: + Minimum Education Requirement: Bachelor's Degree + Experience Requirement: at least a year of direct clinical research/clinical trial experience is… more
- Guthrie (Sayre, PA)
- …Ensure IRB operations align with federal (OHRP, FDA), state laws and institutional policies. Provides guidance to the IRB in developing policies and ... procedures, interpreting regulations, obtaining Foundation Board approval of new IRB members, and...to safeguard ethical research conduct. 2. Research Governance & Institutional Integration + Serve as the Director of Research… more