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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.
$140,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Those responsibilities will include but are not limited to: lab setup bull Laboratory Information Management System LIMS data entry Pre-clinical sample handling and shipping preparation bull Handling of preserved tissue and preparation for histology processing Must be able to sit or stand for extended periods.
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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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Clinical Research Associate. Support or lead clinical research study start up activities (includes creation of study binders, study logs, work instructions, case report form, and other study related materials.
ExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements.
$160,000 a yearFull-timeWork from homeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Data Review: Review and verify the accuracy and integrity of clinical trial data, ensuring timely data entry and resolution of queries. We are seeking a Contract Clinical Research Associate (CRA) specializing in cardiology trials to join our dynamic research team.
$80 an hourFull-timeRemoteExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Under direct supervision, responsible for coordinating and participating in clinical research studies conducted by principal investigator, to include recruitment, collection, compilation, documentation and analysis of clinical research data.
Part-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The research team is engaged in clinical research with functional magnetic resonance imaging on a potential mechanism underlying ketamine treatment. Other responsibilities will include maintaining scientific protocols, assisting at functional magnetic resonance imaging sessions, data entry and data management.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Completes data entry into sponsor-specific data entry systems and/or supports data coordinator, including query resolution. Coordinates and oversees patient (study participant) activity as it relates to the conduct of research and clinical trials including informed consent under direction and supervision of more senior research staff.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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The Research Data Associate will ensure the accurate execution of the study protocol in accordance with Good Clinical Practices, HIPAA, and IRB. The Research Data Associate will be primarily focused on participant study recruitment and post-recruitment tasks such as collecting follow-up surveys, and data entry.
$48,846.72 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Role: Clinical Research Associate (CRA) - A. Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), Contract Research Organization (CRO) selection and management, selection and training of investigator sites, planning and running study meetings, evaluation, selection and training of new study investigators and writing and assembling submissions.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Screening, consenting and data entry for clinical trials. The IR Research Associate will be involved in all Vascular and Interventional Research Projects covered by the Service Line. Will create ideas and collaborate with faculty for prospective or outcome based retrospective research as well as work as a coordinator in department, industry or NIH sponsored clinical trials.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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5 years experience in clinical research and data related fields. Perform data entry, conflict resolution and run reports analyzing measurement changes over time. Communicate feedback on submissions and issue queries to clinical sites regarding image quality, data discrepancies, assessment results and changes in image collection procedures, on a timely basis.
Full-timeExpandApply NowActive JobUpdated 15 days ago
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