- 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 ... (PI), study team and Sponsor/CRO. This position will report directly to the Program Manager and work directly with PIs and clinical research nurses (CRNs). The CRC… more
- University of Pennsylvania (Philadelphia, PA)
- …with minimal supervision, prepare and process all regulatory documentation through the IRB , CTSRMC, FDA and all applicable regulatory review committees- ... work as part of a team, as well as independently; knowledge of IRB and human research protection regulations, including ICH GCP guidelines. The successful candidate… more
- University of Pennsylvania (Philadelphia, PA)
- …also include: transporting specimens, submission of study documents to all applicable institutional committees (eg, IRB , CTSRMC, IBC, CHPS) for initial approval, ... will report directly to the Lead Nurse and Team Manager and work directly with Physician Investigators ("PI") on...team in order to obtain guidance or assistance. + Review all clinical and laboratory data and adverse events,… more
- UPMC (Pittsburgh, PA)
- …of oncology-focused trials at Hillman. These trials include institutional (investigator-initiated), multi-center cooperative group/National Clinical Trial Network ... study development and implementation assistance, submissions to the FDA, IRB processing, patient recruitment, study coordination, study-specific training, data… more
- Carnegie Mellon University (Pittsburgh, PA)
- …**Research Program Administration:** + Assist the Principal Investigator or Project Manager /Director with timeline and resource management to ensure timely delivery ... supports research compliance requirements on supported awards includinghuman subjects ( IRB ) and animal (IACUC) protocols, clinical trials, export controls, andother… more
- University of Pennsylvania (Philadelphia, PA)
- …of study documents. Communicate with study team members and regulatory review boards. Recruit, consent and screen patients according to protocol. Schedule ... or CRO, includes source documentation, case report forms, and research charts. Collect, review and report study data. Complete case report forms and resolve data… more
- University of Pennsylvania (Philadelphia, PA)
- …research administrative activities in support of the principal investigator, project manager and other key stakeholders. May provide support for multi-year grant ... Recruit, schedule and run research subjects; execute subject payments. + Assist with IRB prep and grant prep. + Order supplies and maintain study databases; maintain… more
- Geisinger (Danville, PA)
- …will coordinate with other team members (eg, Staff Scientist, Statistician, Project Manager ). + Develops and leads research projects within the defined scope of ... position may also be sent to the same address. Review of applications will begin immediately and will continue...this includes Geisinger groups such as clinical departments, the IRB , and the compliance, quality, and legal functions +… more
- University of Pennsylvania (Philadelphia, PA)
- …Research coordinator work includes study design, protocol development, submission to review boards, subject recruitment and enrollment, study visits and regulatory ... of study documents. Communicate with study team members and regulatory review boards. Recruit, consent and screen patients according to protocol. Schedule… more