- University of Pennsylvania (Philadelphia, PA)
- …a wide spectrum of clinical trials ranging from phase I to IV, investigator and industry initiated trials. Research coordinator work includes study design, protocol ... to review boards, subject recruitment and enrollment, study visits and regulatory compliance in one or more studies. This position is responsible for study… more
- OhioHealth (Columbus, OH)
- …investigators and outside sponsors concerning status of IRB approval. Quality and Compliance Assists in audit preparedness activities for OHRI. Assists with ... across OhioHealth research sites. The person in this position provides compliance oversight and guidance and communicates and interprets agency policies and… more
- Stanford University (Stanford, CA)
- Research Assistant ( 2 Years Fixed-Term) (Multiple Positions) **School of Medicine, Stanford, California, United States** Research Post Date Oct 03, 2025 Requisition ... students, research scientists, and research assistants. This is a 2 -year position. The goal of the research in the...procedures. Analyze and summarize results for review with supervisor. Audit the accuracy and validity of data. + Review… 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
- Georgetown Univerisity (Washington, DC)
- …dedication to making a difference in the world. Requirements The Research Data Coordinator 2 (DC 2 ) position is responsible for data management for phase I, ... research protocols including, but not limited to, industry, national, and investigator -initiated studies. + Accurately capture data in electronic or paper Case… more
- Covenant Health Inc. (Knoxville, TN)
- …study-related events to the research team immediately. Effective communication with investigator and sponsor representative to ensure protocol compliance . ... protection. In addition, the Clinical Research Nurse Coordinator assures compliance with protocol and regulatory requirements, manages patient protocol activities,… more
- Rush University Medical Center (Chicago, IL)
- …studies, single site studies, intergroup studies, industry studies, and investigator initiated studies. Prepares internal and external regulatory submissions ... with Rush policies and procedures. **Required Job Qualifications:** * Bachelor's degree. * 2 -4 years clinical experience * 2 years coordinating Human Subjects… more
- Guthrie (Sayre, PA)
- …expenses. + Manage pharmaceutical and federally funded study contracts, billing compliance , and audit preparation. + Maintain dashboards to monitor ... a senior administrative executive to collaboratively lead the strategic, operational, and compliance functions of DGF. This role is central to ensuring the effective… more
- University of Utah (Salt Lake City, UT)
- …preparation of all necessary regulatory documents related to the study protocol. 2 . Oversees compliance to protocol; manages quality control, completion and ... of research studies while accomplishing study objectives and for maintaining compliance with guidelines set by government agencies. Examples of responsibilities… more
- University of Pennsylvania (Philadelphia, PA)
- …wide spectrum of clinical trials ranging from phase I to IV, investigator and industry initiated, different disease states and varying complexities. Research ... to review boards, subject recruitment and enrollment, study visits and regulatory compliance in one or more studies. Our projects occur throughout the Department… more