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Responsible for completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB. Provides limited patient contact as needed for study and assist with study budget and patient research billing.
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Register, compile and submit data; monitor research study compliance; maintain a system for effective research data flow and regulatory documentation; open and maintain clinical studies for subject accrual; prepare, submit and file appropriate regulatory documents; update consent form and protocol documentsPatient Care & Enrollment.
$27.5 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Position Summary The clinical research associate will support neuroimaging studies of anxiety, alcohol use disorder, and/or autism in the Blackford Laboratory. Required Computer Applications: Not Applicable Required Other Computer Applications: Required Additional Knowledge, Skills and Abilities: Preferred Education: Bachelor's degree If any degree/training is preferred, please specify the type: Psychology or Neuroscience Preferred Experience: Experience related to clinical research, especially in mental health and/or neuroimaging.
$63,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Join us as a Clinical Research Associate, where you'll manage multiple research protocols to ensure efficiency and regulatory compliance while attending clinics as needed. As a successful candidate, you will:·Manages and maintains protocol documentation and regulatory documents for IRB, DSMB, and PRMC/CPRMC.·Compiles, submits, and processes data and specimens per protocol requirements, ensuring accuracy and safety.
$32 - $40.34 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Coordinates non-therapeutic (i.e., minimal risk, survey, chart review) clinical research protocols with direction from the Principal Investigator and/or senior staff in compliance with regulatory laws and institutional guidelines.
$69,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Positions in this family perform basic, translational, and/or clinical research towards solving a specific problem for an entity or community. Includes Clinical roles focused on research projects.
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Enroll, register and screen patients for Oncology clinical research trials; collect and submit clinical trial patient data. Job Summary:The Clinical Research Associate I will coordinate Oncology research trials for the Cancer Center and associated satellite sites, primarily involving investigational medications and treatments, including early or late phase FDregulated trials.
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Our global Clinical Operations colleagues within our PPD® clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts.
$157,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Experience with database, data management, FDA regulations, IRB requirements and the Stanford clinical research environment highly desirable. Collect and manage patient and laboratory data for clinical research projects.
$36.54 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Preferred Education, Experience and Skills: Proven experience conducting and supporting all phases of research in a clinical environment including data management and analyses. Position Focus: Research Associate will be working on different clinical trials for the PI that include screening, consent, blood draws, hemodynamic monitoring, processing of blood draws as specified in protocols, and follow ups.
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Position Summary: We are currently seeking a dedicated and experienced Clinical Research Associate II (CRA II) to join our team. Minimum of 2 years of experience as a Clinical Research Associate, preferably in a CRO or pharmaceutical setting.
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IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
$174,468 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The PositionThe Sr. Clinical Research Associate (Sr. CRA) provides support to Study Lead(s) in clinical study planning, execution and management. Assist in the preparation of training materials and presentations related to study executionProvide updates on study/site status as needed to ensure timely study entry and updates are reflected on ClinicalTrials.gov or equivalentPerform periodic data review as requested by the Study LeadSupport Study Lead in preparing materials for study-wide meetings (eg investigator meetings, interim update meetings, data safety committee meetings, etc.
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Clinical Research Associate/ CTMPosition Summary: The Clinical Research Associate (CRA)/ CTM will oversee and manage clinical trials to ensure compliance with regulatory requirements and study protocols.
$156,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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For Research Investigator, with Ph. D. approximately 0-2 years experience with demonstrated progression clinical pharmacology and Pharmacometrics. For Sr. Research Investigator, with Ph. D. approximately 2+ years experience with demonstrated progression clinical pharmacology and Pharmacometrics.
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clinical research data jobs Title: clinical research associate
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