- University of Pennsylvania (Philadelphia, PA)
- …and presentations, and to publicize the project's results. + Develop and maintain IRB protocols at Penn; assist Brazilian collaborators with IRB documents for ... tasks, including meetings with collaborators and external groups, such as advisory board meetings. Required Qualifications + Bachelor's Degree in related field + At… more
- University of Pennsylvania (Philadelphia, PA)
- …studies are conducted safely and according to protocol; coordinating the IRB process; implementing projects; working closely with leadership on grants submissions; ... RECOVER clinical research database. + Will assist with coordinating IRB documents. Act as a resource to PI and...Act as a resource to PI and CRS regarding IRB process and protocols. Responsible for document management, ensure… more
- University of Pennsylvania (Philadelphia, PA)
- …as developing study documents (protocol, informed consent, CRFs), obtaining single IRB approval, preparing meeting materials and presentations, and designing and ... the study team (Steering Committee, investigators, study staff, consultants, the IRB , industry sponsors and NIH), managing operations, timelines, and working with… more
- University of Pennsylvania (Philadelphia, PA)
- …more. This individual will also be responsible for ensuring compliance with all IRB , sponsor, and institutional regulations and guidelines. There will be ... the Research Project Manager in submitting documents to regulatory authorities (eg IRB , FDA, etc.) and/or review /monitoring boards (ie, DSMB, independent safety… more
- University of Pennsylvania (Philadelphia, PA)
- …are maintained in a secure manner. + Resolve regulatory related queries with IRB , study sponsors. Review Research bills/invoices for accuracy for payment from ... in a secure manner. + Resolve regulatory related queries with IRB , study sponsors. Review Research bills/invoices for accuracy for payment from research revenue… more
- University of Pennsylvania (Philadelphia, PA)
- …A high degree of autonomy, leadership, and expertise in GCP and institutional policies is expected. QUALIFICATIONS: Clinical Research Coordinator B + Bachelor's ... + Flexible, detail-oriented, and able to multitask effectively + Familiarity with IRB processes and human subject research regulations + Position contingent upon… more
- Norstella (Harrisburg, PA)
- …the product meets customer needs and project goals. + Maintain familiarity with IRB , EC approval requirements, and GCP guidelines to ensure each project complies ... trial life cycle & processes, industry standard patient recruitment strategies, IRB /EC approval requirements, and GCP guidelines is a plus. + Detail-oriented… more
- Norstella (Harrisburg, PA)
- …our solutions. + Ensure all work complies with relevant regulatory requirements (eg, IRB , EC, GCP) and data privacy standards. + Mentor junior project managers and ... of clinical trial operations, patient recruitment strategies, regulatory requirements ( IRB /EC), and GCP standards. + Proficiency in project management tools… more
- Penn Medicine (Lancaster, PA)
- …conducting research studies and clinical trials per Federal, State and Institutional guidelines. The Trauma Research Associates responsible for all research related ... activities including development of IRB approved research and clinical studies trials site operational...delegation in conducting clinical studies trials per Federal and institutional guidelines. + Responsible for the coordination of research… more
- University of Pennsylvania (Philadelphia, PA)
- …in accordance with Good Clinical Practices, HIPAA, and other federal/ institutional requirements, and (2) meet required obligations to patients/subjects, Principal ... processes for Industry-sponsored, Cooperative Group, and Investigator-initiated studies; proactively review protocols and associated manuals, ask questions, and pursue… more