- Wayne State University (Detroit, MI)
- …(job duties): Job Purpose: Under the direction of the Principal Investigator , provide scientific and technical assistance to complete laboratory based, clinical ... and interviewing candidates. Participate in implementing research objectives, ensuring compliance with all legal, regulatory and protocol guidelines. Assist staff… more
- University of Utah (Salt Lake City, UT)
- …to patients and families. The Clinical Research Coordinator assists the Primary Investigator in all IRB and regulatory submissions and clinical coordination specific ... control and completion of research studies while assisting the Principal Investigator in determining and accomplishing study objectives. The Clinical Research… more
- Vanderbilt University Medical Center (Nashville, TN)
- …occasional weekend work. Under the guidance and supervision of the Principal Investigator , the Research Nurse Specialist II (RNS II) is responsible for assuring ... the trial from screening to randomization to study completion, ensures compliance with protocols and overall research and clinical objectives, manages study-related… more
- SUNY Upstate Medical University (Syracuse, NY)
- …Health, including early to late phase FDA-regulated trials, and ensure compliance with federal guidelines. Interact and correspond with clinicians, sponsors, ... to work as a team member on behalf of more than one investigator . Preferred Qualifications: Experience with patient recruitment and enrollment preferred. SOCRA CCRP… more
- Mount Sinai Health System (New York, NY)
- …questionnaires. + Obtain informed consent under supervision of the study investigator (s) * Educate potential participants regarding study requirements. + Screen ... through medical record review + Coordinate research team to ensure compliance with planned treatment protocol including required laboratory and radiographic testing.… more
- Mount Sinai Health System (New York, NY)
- …through medical record review + Coordinate research team to ensure compliance with planned treatment protocol including required laboratory and radiographic testing ... as required by protocol + Act as liaison between investigator and study sponsor + Coordinate activities pertinent to...appointed monitors to ensure accuracy of subject data and compliance with research protocol + Maintain source documents and… more
- Guthrie (Sayre, PA)
- …a senior administrative executive to collaboratively lead the strategic, operational, and compliance functions of DGF. This role is central to ensuring the effective ... oversight responsibilities across core domains: + Clinical Research Operations in compliance and in regulatory areas. + Supports research and scholarly activities… more
- Mount Sinai Health System (New York, NY)
- …questionnaires. + Obtain informed consent under supervision of the study investigator (s); educate participants regarding study requirements. + Screen patients for ... subjects with sponsoring agency. + Coordinate research team to ensure compliance with planned treatment protocol including required laboratory and radiographic… more
- University of Pennsylvania (Philadelphia, PA)
- …processing/handling. The CRC will demonstrate vigilance in patient safety, protocol compliance , and data quality, and will participate in data organization for ... performed, reporting adverse events and ensuring review and appropriate follow-up by investigator , monitoring patient care and treatment side effects in concert with… more
- Dartmouth Health (Lebanon, NH)
- …research and a full range of clinical research duties including regulatory compliance . * May arrange/schedule required tests and other appointments. * Independently ... of the study operations (subject management/regulatory) with minimal oversight from the investigator or their designee. * Oversees subject management, such as data… more