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Reviews study with principal investigator and/or clinical research coordinator to a budget outlining standard of care and research costs. In collaboration with the principal investigator, clinical research coordinator, and clinical team, participates in the review of studies for feasibility and evaluates potential competition with other protocols prior to submitting study.
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The primary responsibility of the Clinical Research Coordinator B (CRCB) in the Department of Ophthalmology is to implement one or more industry sponsored, NIH or investigator initiated clinical trials assuring each study is conducted per protocol and adheres to ICH/GCP guidelines.
$43,919 - $66,183 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Along with the investigator, the Clinical Research Coordinator will screen, enroll and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study.
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The Clinical Research Associate / Marriage and Family Therapist will be responsible for practicing a standardized cognitive behavioral intervention as part of a federally-funded study of nonpharmacological treatment for headache attributable to mild traumatic brain injury.
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As a Clinical Research Associate I, you will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the study.
$19.5 - $29.87 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study.
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Join us as we continue to grow, the Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes & procedures, and in compliance with FDA, GCP, and ICH regulations and guidelines.
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The Clinical Research Coordinator assists the investigator team to develop study protocols and manuals of procedures. The Clinical Research Coordinator screens, enrolls and follows study participants, conducts data collection and entry, and performs noninvasive cardiovascular tests according to study protocols.
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Directly involved with study start-up, implementation, conduct, and close-outs. Completes applications and obtains appropriate approvals from various groups for all necessary study start-up functions.
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Years’ experience: Minimum of two (2) years’ experience coordinating research protocols OR (2) years' experience in cancer research OR certification as a Certified Clinical Trial Investigator (CCTI), Certified Clinical Research Coordinator (CCRC), or Certified Clinical Research Professional (CCRP) from the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SoCRA.
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The Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Principal Investigator (PI; Dr. Martinez); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.
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Accurately reviews all study activities prior to activation; successfully arranges site initiation visits, monitoring visits, and close-out visits; disseminates new information to research staff, pharmacy staff, and principal investigator in a timely fashion.
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Join other professionals revolutionizing efficient and seamless study start-up to advance clinical trials. This position works both independently and collaboratively with a team to meet common goals and plays a key role in the clinical trial management and study start-up process at Medpace.
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In collaboration with the Principal Investigator, conducts research studies as outlined in the study protocol; discerns critical elements of the protocol to ensure subject safety throughout the study; adheres to good clinical practices.
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We are extremely active in the Childhood Arthritis and Rheumatology Research Alliance (CARRA) and its sub studies, as well as investigator-initiated and pharma-funded research and have a full-time clinical research coordinator and access to other research support through the pediatrics department.
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clinical research investigator study start up jobs Company: Cedars Sinai
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