- University of Pennsylvania (Philadelphia, PA)
- …patient/participant information* Assisting or leading in the preparation and submission of IRB documents Coordinator A: Assist in the coordination of federally ... wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator A/B Job Profile Title Clinical Research Coordinator A Job… more
- Guthrie (Sayre, PA)
- …Other Duties: + Collaborate with executive director, manager, research team members and IRB coordinator in developing and revising process flow for research ... Responsibilities for program development include assisting with feasibility, site selection, IRB document review , and corresponding with investigators, IRB… more
- University of Pennsylvania (Philadelphia, PA)
- …programs and resources, and much more. Posted Job Title Clinical Research Coordinator A (Department of Emergency Medicine) Job Profile Title Clinical Research ... Coordinator A Job Description Summary Clinical Research ...are conducted safely and according to protocol; coordinating the IRB process; implementing projects; working closely with leadership on… more
- University of Pennsylvania (Philadelphia, PA)
- …wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator A/B Job Profile Title Clinical Research Coordinator A Job ... data collection and management, and potentially some regulatory responsibilities. The coordinator must be detail oriented and have prior experience 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)
- …wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C Job Profile Title Clinical Research Coordinator B Job ... team meetings. Prepares and submits regulatory documents to the IRB . Additional duties include regular office duties (eg scanning...contingent upon funding. * CRC-B: Bachelor of Science and 2 to 3 years of experience or equivalent combination… more
- University of Pennsylvania (Philadelphia, PA)
- …adverse events according to regulatory requirements. + Prepares all documents for IRB review including draft informed consents written for subject reading ... by study sponsors. Qualifications + Bachelor of Science and 2 to 3 years of experience or equivalent combination...lab cardiology nurses. + Support and train new research coordinator . + Review all new trials in… more
- University of Pennsylvania (Philadelphia, PA)
- …programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C (Department of Medicine) Job Profile Title Clinical Research Coordinator ... and industry initiated, different disease states and varying complexities. Research coordinator work includes study design, protocol development, submission to … more
- University of Pennsylvania (Philadelphia, PA)
- …programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C (Division of Infectious Diseases) Job Profile Title Clinical Research ... Coordinator B Job Description Summary As part of the...study documents. Communicate with study team members and regulatory review boards. Recruit, consent and screen patients according to… more
- WellSpan Health (York, PA)
- …for clinical research patients. **Essential Functions:** + Participates in the review of research protocols and assesses the appropriateness, feasibility and ... consent documentation requirements are met as per the GCP, FDA and IRB guidelines. Registers and accomplishes randomization of patients enrolled in research studies.… more