- University of Miami (Plantation, FL)
- …Form and all source documentation required to determine eligibility and maintain compliance . 14. Works closely with the Investigator , Investigational Pharmacist, ... Identifies desired research outcomes and evaluates and monitors subjects' responses. 3 . Conducts initiation visits and registers patients in clinical studies.4.… more
- Dartmouth Health (Lebanon, NH)
- …healthcare/clinical research compliance and quality assurance. * Minimum of three ( 3 ) years of management experience in a clinical research compliance ... for the administration, support, quality assurance, and management of research compliance functions for the Office of Clinical Research (OCR). This position… more
- The County of Los Angeles (Los Angeles, CA)
- …records, and other related areas, and prepares comprehensive reports on audit findings. CLASSIFICATION STANDARDS Positions allocable to this class are located ... practices, policies and procedures, focusing on high-risk areas and its compliance to policies and procedures; determining whether internal controls are adequate… more
- Xcel Energy (Minneapolis, MN)
- …**Essential Responsibilities** + Support and manage activities associated with the Compliance Hotline. Assign new cases to appropriate investigator and ... for. **Position Summary** Support the day-to-day operations of the Corporate Compliance and Business Conduct program, in accordance with the Federal Sentencing… more
- Guthrie (Sayre, PA)
- …expenses. + Manage pharmaceutical and federally funded study contracts, billing compliance , and audit preparation. + Maintain dashboards to monitor ... is the research arm of The Guthrie Clinic and operates as a 501(c)( 3 ) nonprofit organization. Its mission is to support, facilitate, and grow high-impact clinical,… more
- University of Utah (Salt Lake City, UT)
- …of research studies while accomplishing study objectives and for maintaining compliance with guidelines set by government agencies. Examples of responsibilities ... all necessary regulatory documents related to the study protocol. 2. Oversees compliance to protocol; manages quality control, completion and submission of study… more
- AT Still University (St. Louis, MO)
- …collection, and data organization and storage. This part-time position will be in-office 3 days per week. The Research Coordinator will report to the Director of ... Oral Medicine, Dental Oncology and Urgent Care and Principal Investigator . Requirements **Major Job Duties** + Coordinates with Principal Investigator (PI),… more
- Dana-Farber Cancer Institute (Brookline, MA)
- The Regulatory Coordinators (RC) works under the direction of the Principal Investigator (s), Clinical Research Manager and / or directly for the Clinical Trials ... regulatory documents, and maintains records on assigned studies to ensure regulatory compliance with DFCI and DF/HCC policies as well as federal regulation and… more
- University of Utah (Salt Lake City, UT)
- …details involved in both sponsor and physician-initiated clinical research studies; and ( 3 ) assist the Principal Investigator and study team in achieving ... informed consent documents under the supervision of the study investigator . 3 . Attend and actively participate in...out and prepare summary report for sponsor. 11. Complete, audit , correct, and relay case report forms (CRFs) to… more
- Banfield Pet Hospital (Vancouver, WA)
- …made possible by 75,000 Associates who care for millions of pets across nearly 3 ,000 clinics in more than 20 countries each year. We are committed to leveraging ... study sites to support and provide guidance on the administration of the compliance , financial, personnel and other related aspects of the clinical study. Essential… more