Assists th Clinical Research, Research Coordinator, Clinical, Coordinator, Research, Clinic, Healthcare. This position will be responsible for the coordination of multiple research studies/clinical tr...
read moreMay be required to perform venipuncture on study participants; collects, processes, and ships specimens according to protocol and training requirements Research Coordinator, Clinical Research, Clinica...
read moreTwo or more years of experience in clinical research (can include experience gained during M. Execute the laboratory-based clinical research strategy and program at GSSI’s research hub in Valhalla, NY...
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 moreDemonstrated experience in clinical research coordination or related roles, with a strong understanding of research. Join our dynamic pulmonology research team as a Research Coordinator, where you wil...
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 moreThe Mount Sinai Health System believes that diversity, equity, and inclusion are key drivers for excellence.We share a common devotion to delivering exceptional patient care.When you join us, you beco...
read moreInstitutional Review Board, Grants, and Contracts Office), and provides clerical support to Clinical Research Coordinators and others in assigned areas. Clinical Research Coordinator (CRC). S/he is th...
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 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 moreSOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). Minimum of 2 years experience in a Seni...
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 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). In collaboration with the principal inv...
read moreAt least two (2) years of clinical or clinical related or research related experience Required. At least three (3) years of clinical or clinical related or research related experience Preferred. Under...
read moreSupervise other coordinators working with the investigator and ensure that the research team is updated and provided with the most current data regarding patient enrollment and study procedures. Work ...
read moreExperience working on a collaborative team and interacting directly with patients in clinical and/or community settings.
Conduct clinical investigation utilizing GCP, which includes possessing and demonstrating knowledge of federal regulations and guidance documents for the conduct of clinical studies involving human su...
read moreAssist in analyzing clinical data to determine response and clinical outcomes; contribute to the preparation of study abstracts, posters, manuscripts and grant applications. The CRC will be responsibl...
read moreClinical Research Coordinator work includes study design, protocol development, submission to review boards, subject recruitment and enrollment, study visits and regulatory compliance in one or more s...
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