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The Clinical Research Coordinator may coordinate device and drug treatment research trials, as well as observational studies conducted at Children's Medical Center, including but not limited to study set-up, implementation, fiscal monitoring, and data collection/entry.
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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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The Clinical Research Coordinator assists the clinical trials process by registering hematology, oncology, and bone marrow transplant patients for clinical studies, assessing eligibility criteria, maintaining current protocol packets and assuring that all quality assurance measures are maintained within the protocol/study.
$39,300 - $64,349 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Onsite) FUNCTION: Clinical Operations – Biomarker and Bioanalytical Operations Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all Company therapeutic areas.
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4 years of clinical research experience in the academic or pharmaceutical clinical trials environment. Relevant certification as a Certified Clinical Research Professionals (CCRP), Certified Clinical Research Associate (CCRA), Certified Clinical Research Coordinator (CCRC), or Certified IRB Professional (CIP) upon hire or within six months of hire.
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As a Junior Clinical Research Coordinator, you are responsible for assisting with the management and coordination of all aspects of conducting clinical trials within s RII, surgery centers, both clinically and administrative/regulatory.
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This position will manage activities pertaining to the Protocol Review and Monitoring Committee (PRMC) which primary goal is to ensure that institutional, industry-sponsors, and externally peer reviewed cancer research studies involving human subject conducted under the auspices of the SCCC are (1) scientifically and statistically sound; (2) appropriately designed; (3) feasible for completion; and (4) if applicable, in compliance with NIH guidelines for clinical trials.
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OHSU is well equipped with a state-of-the-art neuroimaging center, outstanding core facilities and laboratories, a strong pre- and post-doctoral training infrastructure, and proximally-housed developmental and clinical researchers with ample space for human subjects study data collection.
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The Rater is responsible for the organization, administration, management, and efficient execution of clinical ratings associated with clinical trials. Excellent communication skills (interpersonal, written, verbal) Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as Study Manager.
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Posted Job TitleClinical Research Coordinator A/B (Palliative Research Center)Job Profile TitleClinical Research Coordinator AJob Description SummaryThe Palliative and Advanced Illness Research Center is seeking a full-time clinical research coordinator who will be responsible for supporting multiple components of a mixed-methods study that aims to design a novel outcome measure for future trials of patients with acute respiratory failure (ARF.
$37,220 - $65,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Our activities extend from exploratory biology to the identification and validation of therapeutic targets, and from drug discovery and development to clinical studies and trials. · Work with biorepository and animal breeding managers to ensure: a) that materials are available and can be provided for a given study prior to the execution of contracts; and b) that materials generated by collaborators are properly registered in CHDI’s databases, consequently tracked and deposited.
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Maintain effective professional communication with Primary Investigator, NIH scientists, site investigators, clinical and laboratory study teams, to assist in prioritizing laboratory assays for vaccine trials.
$40,100 - $70,180 a yearFull-timeExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Responsible for the compilation of all data for clinical trials managed by the CTO. Manages project data including extraction, entering, processing, accuracy, analysis and evaluation of data ensuring that results meet project information and deliverable objectives.
$49,500 - $58,140 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Assists investigator with consent process assuring patients understand clinical trials. Knowledge of clinical trials and the regulation (local, state, and federal) of such.
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Evaluation & Implementation of Clinical Trials: Review study protocols, primary disease category and investigational drug information; Familiarity with all study requirements; Communicate and make arrangements with the different areas of AU that may be involved in the study (ice radiology, laboratory services, pathology, patient scheduling, etc.
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