- University of Colorado (Aurora, CO)
- …+ Adhere to research regulatory standards + Maintain detailed records of studies to ensure compliance with requirements, study protocols, department, ... to protocols, informed consent forms, and all other essential study documents for assigned studies + Independently...all other essential study documents for assigned studies + Independently perform study related processes,… more
- ARTIDIS (Houston, TX)
- …(CRAs) and Clinical Study Managers (CSMs) to ensure that all clinical studies comply with the approved study protocols and that Good Clinical Practice ... and contractual requirements. SCRAs work on all aspects of clinical studies in ARTIDIS's study sites globally, providing specific oversight on clinical study … more
- Johns Hopkins University (Baltimore, MD)
- …and scientific implementation of clinical protocol for a complex* and/or multiple research studies . As part of the study team, collaborates with faculty to ... develop protocols, develop SOPs, and oversee study -related activities for one or more complex studies . (*Complex to include studies with investigative drugs… more
- ThermoFisher Scientific (Wilmington, NC)
- … documents in support of the regulatory filing** **Responsible for overseeing study financial reconciliation** **Ensure studies are "inspection ready" at all ... Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** **CSM (Clinical Study Manager):** **OBJECTIVES:** **Lead or support study operational… more
- University of Colorado (Aurora, CO)
- … studies to ensure compliance with requirements of funders, study protocols, department, hospital/clinical standard operating procedures and other regulatory ... limited to protocols, informed consent forms, and all other essential study documents for assigned studies + Develop, with assistance from study teams,… more
- Merck (Rahway, NJ)
- …function is to design, coordinate, monitor, and report clinical laboratory and field studies that will support the regulatory approval of new companion animal and ... responsible for the conduct of Good Clinical Practice (GCP) studies , and occasionally Good Laboratory Practice (GLP) studies.... The Associate Principal Scientist is the primary clinical study team leader and has overall responsibility for a… more
- University of Colorado (Aurora, CO)
- …a program manager over both epidemiological observational studies and RCT/intervention studies and multi-site study coordination + Expertise in the area of ... Management** + Oversee all aspects of four multi-site research studies in coordination with the Principal Investigator and partner...studies : 1) three R01s encompassing a longitudinal cohort study with 1307 families and a sub- study … more
- Stanford University (Stanford, CA)
- …on "bench to bedside" technology. The primary work will include supporting pilot studies of Pediatric Gastroenterology faculty (from study start up to closure), ... Associate (CRCA) to perform duties related to the coordination of clinical studies withintheStanford Medicine Children's Health Center for Pediatric IBD and Celiac… more
- University of Colorado (Aurora, CO)
- …including but not limited to protocols, informed consent forms, and all other essential study documents for assigned studies + Independently perform study ... + Assist with and oversee the day-to-day operations of clinical trials and studies + Manage and conduct moderately complex research activities that are part of… more
- University of Utah (Salt Lake City, UT)
- …studies while- assisting the Principal Investigator in determining and accomplishing study objectives. Oversees research studies in an administrative and ... Coordinates technical and administrative details involved in research or clinical studies . + Exposure to study the development of full study life-cycle from … more