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Create and maintain all essential documents for each study (ICF, enrollment logs, source docs, phone screen) Collection of labs (drawing blood, performing EKG’s, collecting vitals) and maintaining good communication with patients.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Writes patient information sheet (ICF) for clinical studies for admission to IRB, as well as. The Clinical Research Coordinator must also be able to perform clinical. ● Writes patient information sheet for clinical studies for submission to IRB, as well as.
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Relevant experience in one or more of the following healthcare areas preferred:Coordination of community resourcesCare management of diverse patient populationsAmbulatory Care Knowledge of levels of care throughout the health care continuum to include; inpatient, emergency care, rehab, home health, hospice, long term acute care, SNF, ICF, ALF with an overall understanding of utilization management and resource management.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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2 years of experience as a clinical research coordinator required. Obtain informed consent per Research SOP and document process when revised ICF discussed with patient during course of the trial.
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Background in Clinical regulatory affairs: Clinical study reports, protocols, Investigator Brochure, investigator updates, ICF, IRB, site initiation, sponsor/investigator responsibilities etc.
$109,100 - $141,800Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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We're seeking to partner with International Coaching Federation (ICF) Coaches, Clinical Psychologists, and counsellors to be part of a community working collaboratively to bring greater mental health access to the public to provide mental health coaching.
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Preferably experience in drug/clinical development and/or registry, surveillance studies (e.g. Project Management, Pharmacovigilance, Medical Affairs, RWE, Clinical Pharmacology, study operations.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Provide operational and strategic input into study documents such as synopsis, protocol, ICF, CRFs, CRF Completion Guidelines, Study Execution Plans, Clinical Data Review Plan, Clinical Database edit specifications, Clinical Study Report (CSR) development, etc.
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Job Summary Conduct Person-Centered LTC, ABI, ICF/IID Annual, or ORC assessments in accordance with State directives, MAXIMUS processes, and regulatory timeframes. Job Summary Conduct Person-Centered LTC, ABI, ICF/IID Annual, or ORC assessments in accordance with State directives, MAXIMUS processes, and regulatory timeframes.
Part-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Provides scientific and clinical input to study-related documents and analysis plans including Informed consent forms (ICF), clinical research forms (CRF), statistical analysis plans (SAP), clinical pharmacology analysis plans (CPAP), and clinical study reports (CSR.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Conduct Person-Centered LTC, ABI, ICF/IID Annual, or ORC assessments in accordance with State directives, MAXIMUS processes, and regulatory timeframes. Licensed Clinical Social Worker (LCSW.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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The (Senior) Clinical Trial Manager is accountable for delivery of selected and/or regional activities within a trial (e.g., manage and oversee vendor deliverables, collaborate with functions to set up activities [e.g., DM, IRT, and eRT], support site activation and recruitment, support data review/cleaning activities, support PI/ICF development.
$95,625 - $159,375 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Maintain and update research fund accounting files, research billing, budgets and. complete the necessary documents for IRB submission in a timely fashion. complete the necessary documents for IRB admission in a timely fashion.
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Contribute to the strategic discussion on clinical trial design and developing core clinical trial related documents including but not limited to Informed Consent (ICF), Protocol, and Investigator Brochure (IB.
RemoteExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Study Planning and Execution: Provides input on major milestones of trial, clinical trial plan and contingency planning; Analyzes and updates management on potential risks to study deliverables; Provides input on ICF creation; Oversees recruitment and retention; establishes and implements contingency plans for shortfalls; Consults & recruits members for DSMB and/or adjudication committee setup.
ExpandApply NowActive JobUpdated 5 days ago
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