- CommonSpirit Health (Merced, CA)
- …limited to: research participant recruitment, screening and enrollment; completion of protocol required visits and procedures; collection and reporting of data; ... participants; document informed consent discussion and obtain signatures per protocol , federal, state and institutional requirements. + Coordinate all study-required… more
- Cedars-Sinai (CA)
- …providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating ... compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. Presents… more
- University of Miami (Miami, FL)
- …on the status of research activities, and submits monthly activity logs for protocol .3. Organizes and coordinates community working group meetings for protocol ... for community partners and supervises and oversees research data collection at protocol venues in the community.5. Reviews study progress, identifies areas of… more
- University of Washington (Seattle, WA)
- …compliant with federal and institutional policies. This will necessitate research protocol submissions to various institutional and external IRBs, ongoing tracking ... IRB renewals, submission of annual reviews, modifications to existing protocols, SAEs, and protocol deviations to the appropriate IRB. This position must be able to… more
- CommonSpirit Health (Santa Maria, CA)
- …limited to: research participant recruitment, screening and enrollment; completion of protocol required visits and procedures; collection and reporting of data; ... participants; document informed consent discussion and obtain signatures per protocol , federal, state and institutional requirements. + Coordinate all study-required… more
- Dana-Farber Cancer Institute (Boston, MA)
- …the group's portfolio. + Responsible for the required tracking of all protocol development, submission, review and approval milestones. + Assist with the oversight ... of subject enrollment, protocol treatment and follow-up care processes for protocol patients. + Assist with the oversight of registration of protocol … more
- University of Rochester (Rochester, NY)
- …compilation, registration and submission of data, monitoring compliance with the protocol , adherence to Standard Operating Procedures (SOPs), and all applicable ... documented and meet both internal and external regulations in accordance with protocol guidelines. + Develops source data worksheets specific to each assigned study… more
- Stony Brook University (Stony Brook, NY)
- …SBMC, pharmaceutical sponsor, patient and IRB. + Determine patient eligibility for protocol participation by way of review of patient's medical records. + ... + Ensure that treatments, evaluations, and dose modifications are administered per protocol . + Identify candidates to be enrolled in clinical trials, review present… more
- Cedars-Sinai (Los Angeles, CA)
- …independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and ... for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. Presents study… more
- University of Pennsylvania (Philadelphia, PA)
- …and varying complexities. Research coordinator work includes study design, protocol development, submission to review boards, subject recruitment and enrollment, ... with study team members. Recruit, consent, and screen patients according to protocol . Schedule patient visits and any necessary testing. Conduct patient visits.… more