- University of Pennsylvania (Philadelphia, PA)
- …activities within the Cardiovascular Division of PPMC Responsible for assisting with study coordination and recruitment for industry sponsored studies . Works ... the Cardiovascular Division of PPMC. Responsible for assisting with study coordination and recruitment for industry sponsored studies...in the cath lab, instruct and support investigators and study staff on carrying out clinical protocol… more
- Dartmouth Health (Lebanon, NH)
- …or senior team member. Site and Study Management * Organizes and manages clinical trials and research studies . * Conducts protocol reviews to assess the ... * Understands and supports all of aspects of the study operations (including subject management/regulatory) with oversight from the...team and the value each member can bring to clinical studies . * Performs other duties as… more
- University of Colorado (Aurora, CO)
- …**Duties (all levels):** + Assist with and oversee the day-to-day operations of clinical trials and research studies + Serves as the Primary Coordinator ... compliance with requirements of the Food and Drug Administration (FDA), study protocols, department, hospital/ clinical standard operating procedures and other… more
- University of Pennsylvania (Philadelphia, PA)
- … clinical research studies , including the recruitment and retention of clinical trial participants. Schedules and runs study visits as per protocol. ... Research Coordinator (CRC) is responsible for the execution of clinical research studies as part of the... studies , including the recruitment and retention of clinical trial participants. Schedules and runs study … more
- University of Pennsylvania (Philadelphia, PA)
- …A : BS degree and 1-2 years related experience in research and clinical study methodologies or equivalent combination of education and experience required ... different studies . The tasks involved in these studies include recruitment of study participants including...degree and 2-3 years related experience in research and clinical study methodologies or equivalent combination of… more
- University of Colorado (Aurora, CO)
- …**Key Responsibilities:** + Assist with and oversee the day to day operations of clinical trials and studies , and act as primary coordinator, including team ... **Research Services Clinical Sciences Professional (Senior or Principal)** **Description** **University...to protocols, informed consent forms, and all other essential study documents for assigned studies , and perform… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …CTCwill develop, implement, and coordinate study procedures to successfully manage clinical studies . The Sr. CTC will perform diverse duties requiring ... clinical project team during all stages of a clinical study by carrying out day-to-day ... tackers and logs. + Manages device accountability for clinical studies , including tracking, shipment, and reconciliation… more
- University of Pennsylvania (Philadelphia, PA)
- …trials. Job Description Job Responsibilities CRC-B + Coordinate and conduct clinical studies , includes; subject recruitment, informed consent, chart maintenance ... enrollment, collection and storage of biological samples and related study documents, and collection of clinical data....federal regulations and guidance documents for the conduct of clinical studies and human subject protection +… more
- Texas Health Resources (Dallas, TX)
- …30 days of hire and maintained every 2 years What You Will Do * Conduct clinical studies according to FDA, CFR and ICH regulations and guidelines: from pre- ... positive manner * Develop and implement recruitment strategies for studies ; which include screening potential study subjects...records of the receipt, administration, and return of all clinical supplies (including study drug). Assist in… more
- System One (Ozark, MO)
- …Summary: The Clinical Research Coordinator will oversee the coordination of clinical research studies while providing leadership and guidance to the site's ... Coordination and Operations + Oversee the day-to-day coordination of assigned clinical research studies , ensuring protocol adherence and regulatory compliance.… more
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