Clinical Research Coordinator III (CRCIII) position is to assist principal investigators with conducting human subjects clinical studies related to environmental, occupational, and public health. Rutg...
read moreExecute the laboratory-based clinical research strategy and program at GSSIs research hub in Valhalla, NY. Two or more years of experience in clinical research (can include experience gained during M....
read moreReports to Director of Clinical Trials or Clinical Research Nurse Lead: Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies. PR...
read moreExecute the laboratory-based clinical research strategy and program at GSSI’s research hub in Valhalla, NY. Two or more years of experience in clinical research (can include experience gained during M...
read moreManages submissions to the Institutional Review Board (IRB) Performs additional non-clinical clinical research coordinator duties (eg data collection, obtaining informed consent) as necessary. Clinica...
read moreThe entry level cosmetologist/clinical research coordinator will be trained extensively on methods of clinical evaluations of hair/scalp, skin, nails and more to complete the trials as per study proto...
read moreFunction independently in a clinical research setting and responsible for the complete coordination of assigned clinical research protocols from national research agencies and pharmaceutical corporati...
read moreThe Clinical Research Coordinator I will participate in clinical research activities related to the Mount Sinai Million project, a Mount Sinai Health System-wide initiative to generate genetic sequenc...
read moreFunctions independently in a clinical research setting and responsible for the complete coordination of assigned clinical research protocols from national research agencies and pharmaceutical corporat...
read moreConducts routine and standardized human subjects research using appropriate research or interview techniques specific to subject matter of the research project, under direct supervision of the Princip...
read morePREFER: Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), or certified within 2 years. Function independently in a clinical research setting and responsi...
read moreMinimum of 2 or more years of experience in clinical research as a Clinical Research Coordinator, with experience in patient recruiting/screening/consenting/retention; activation; regulatory complianc...
read moreUsing a lens of equity in all aspects of patient care delivery, education, and research to promote policies and practices to allow opportunities for all to thrive and reach their potential. National I...
read moreThe Clinical Research Coordinator will also work closely with other Clinical Research Coordinators and Physician Assistant to adhere to clinical protocols conducted with study participants focused on ...
read moreMinimum of 1 to 2 years of experience in Clinical Research as a Clinical Research Coordinator, with experience in patient recruiting/pre-screening/consenting/retention; activation; regulatory complian...
read moreCoordinates the synchronization of research activities within the ARJR service under the direction of the ARJR Director and serves as a liaison between the clinicians, research staff, and other resear...
read moreClinical Research Coordinator/Clinical Instructor (HS), Neurosurgery. The Global Neurosurgery Laboratory at SUNY Downstate Health Sciences University is seeking a Clinical Research Coordinator/Clinica...
read moreThe primary purpose of the Clinical Research Coordinator II (CRCII) position is to assist a multidisciplinary and international research team with conducting clinical studies related to tuberculosis a...
read moreSOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). In collaboration with the principal inv...
read moreAdheres to good clinical practice, and complies with regulatory and grant agency requirements; follows protocol as developed and keeps investigator or supervisor informed of developments. Coordinates ...
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