- Emory Healthcare/Emory University (Atlanta, GA)
- …**Description** The Emory Office of Continuing Medical Education (CME) is seeking a Senior Program Coordinator to join the team! Under the direction of ... the associate director, the Sr. Program Coordinator will oversee operations, meeting management and ensure compliance for live continuing medical education… more
- Vitalief (New Brunswick, NJ)
- …Coordinator , with experience in patient recruiting/pre-screening/consenting/retention; activation; regulatory compliance, IRB submissions , data management ... that ultimately benefit patients. We are seeking several problem-solving, enthusiastic Senior Clinical Research Coordinators (as full time, fully benefited Vitalief… more
- University of Washington (Seattle, WA)
- …Gerontology and Geriatric Medicine has an outstanding opportunity for a Research Coordinator to join their team.** **POSITION PURPOSE** The Division of Gerontology ... Geriatric Medicine at Harborview Medical Center has an opportunity for a Research Coordinator to lead and manage clinical trials and studies focused on Alzheimer's… more
- Beth Israel Lahey Health (Boston, MA)
- …the progress of protocols; planning and prioritizing the work. Management of regulatory aspects of the study, including interaction with Institutional Review Board. ... regarding ambiguous or incomplete data. Monitors quality and timeliness of data submissions . Ensures data extracts completed by staff are in compliance with… more
- Johns Hopkins University (Baltimore, MD)
- …the Clinical Research Program Manager, we are seeking a **_Sr. Research Program Coordinator II who_** will be responsible for study site activation and management, ... including regulatory review, site study team training, data monitoring and...+ Assists the Start Up Specialist new study IRB submissions as needed. + Ensures smooth study activation by… more
- Novant Health (Wilmington, NC)
- …requirements related to the conduct of research (FDA, GCP, IRB, ICH). Assures regulatory submissions for all protocols, adverse events, revisions, renewals, and ... Only Registered Nurses will be considered for this position. The Clinical Research Coordinator (CRC) is a professional working under the direction of their Novant… more
- State of Massachusetts (Boston, MA)
- …using data-driven methodologies. . Prepare reports, presentations, and recommendations for senior management and stakeholders. . Track regulatory changes at ... the COMPTROLLER (CTR)* * * *Statewide Payroll Business Engagement Coordinator * *Management Analyst III* * * *FY26 - 001*...business partners. . Monitor and assess the impact of regulatory changes on agency programs and partnerships. . Interact… more
- Stanford University (Stanford, CA)
- …the world of health care in the cancer arena. Reporting to the Pediatric Senior Clinical Research Manager, the Clinical Research Coordinator 2 - Pediatric ... Clinical Research Coordinator 2 - Pediatric Hematology (Hybrid) **School of...identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions , and respond to requests and questions. + Collaborate… more
- Bassett Healthcare (Cooperstown, NY)
- …design teams, contractors, consultants, and internal stakeholders Help prepare and monitor regulatory submissions to agencies like NYSDOH, OMH, and OPWDD ... NFPA, OSHA, and ADA Maintain accurate documentation and participate in regulatory submissions Track budgeting, cost tracking, value engineering, project… more
- Mount Sinai Health System (New York, NY)
- …and regulatory staff in the preparation of new protocol submissions , protocol amendments, and renewals of ongoing clinical trials. + Obtains informed ... under supervision of the Principal Investigator, Clinical Research Manager, or Senior Clinical Research Coordinator for studies enrolling vulnerable subjects,… more
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