Collaborate with the clinical research team to ensure timely pre-screening of potential subjects and active cancer patients for available clinical trials. The primary purpose of the Clinical Research ...
read moreThe Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or se...
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 moreClinical 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 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. Serve a...
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 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 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 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 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 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 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 moreAs a result, we are seeking a talented and enthusiastic Senior Clinical Research Coordinator to join our exceptional team (as full-time, fully benefited Vitalief employee) to support our mission and o...
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 moreSOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). Along with clinical research nurses, ma...
read moreAs a Clinical Research Nurse, you will play a crucial role in initiating and activating clinical trial protocols, ensuring adherence to regulatory and institutional standards, and providing high-quali...
read moreCoordinates and monitors research trials; actively oversees the recruitment of study participants. Adheres to good clinical practice, and complies with regulatory and grant agency requirements, and st...
read morePosition Summary The Clinical Research Coordinator (CRC) will provide support for research activities in the Division of Nephrology. Responsibilities Obtain informed consent Organize and conduct basel...
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