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Collects study specimen according to protocol which may include phlebotomy, processing, and preparation for shipping. Reviews medical records and/or conducts screenings for recruitment of study participants, performs interviews and QOL questionnaires.
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Collect study specimens according to protocol. The Research Coordinator will be responsible for recruiting subjects, scheduling subject appointments, interviewing adults and children using structured psychiatric interviews and neuropsychological tests, assisting in performing MRI scans, processing financial forms and administering informed consent to study participants as well as ensuring quality of data collection and data analysis.
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Be compliant with infection control procedures and environmental safety protocol within a facility. Build a strong occupational therapy program Enhance clinical expertise, professional and management skills through interaction with managers, therapists and other professional staff, self-study, and other continuing education activities.
$1,500 a weekFull-timeExpandApply NowActive JobUpdated 0 days ago - UpvoteDownvoteShare Job
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Clinical study leader (CSL) or major scientific/medical contributor; Provides the strategic direction to BD&O for EDC, edit checks, data quality listings, SAP, DM plan, Reviews patient population and protocol compliance for consistency with study strategy, Develops biomarker strategy in collaboration with TMCP, Collaborates with external KOLs to refine study plans; Prepares and participate in regulatory agency meetings, if applicable.
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Build a strong physical therapy program Enhance clinical expertise, professional and management skills through interaction with managers, therapists and other professional staff, self-study, and other continuing education activities.
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Responsibilities: Occupational Therapist Summary: Provide occupational therapy (OT) and related services for patients while maintaining positive levels of interaction with facilities and clients in accordance with the principles and practices of occupational therapy and within Reliant Rehabilitation guidelines.
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This role assists in the day-to-day operations of clinical research protocol implementation, and carries out study coordination duties from protocol initiation to study close-out according to regulatory/sponsor guidelines.
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The Patient Recruitment Specialist will mainly be responsible for phone screening potential study participants, entering information into the clinical database, and scheduling potential participants for on-site visits.
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Expanding its immuno-oncology phase I basket study evaluating its product in combination with. A proposed protocol pathway for immuno-oncology will be. Nanobiotix first received authorization to start the pilot phase I/II clinical study in humans in.
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Coordinate research projects, clinical trials, and perform duties as required by the protocol. Responsible for recruiting, screening & enrolling patients in study protocols. Coordinate research projects, clinical trials, and perform duties as required by the protocol.
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Assists in the preparation and submission of regulatory documents to the study sponsor and IRB, as required by the protocol and regulatory requirements. Assist in the conduct and documentation of study visits and protocol-specific testing/interviews according to the study protocol.
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Partners directly with or guides staff to partner with preclinical, regulatory affairs, medical monitor, biometrics, and medical writing to develop protocol and study designs and other key study and program deliverables.
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As a leading rehab therapy provider for skilled nursing facilities (SNFs), Reliant therapists provide necessary rehabilitation services for our most vulnerable population. Ability to read, write, speak, and comprehend in English: instructions, correspondence, charts, memos, and reports Qualifications: Education/Experience: A graduate of an APTA accredited school of physical therapy Computer Skills: Computer literate and proficient in clinical documentation Basic Internet navigation skills Certificates and Licenses: Valid physical therapist state license Interested in learning about us or other opportunities.
$45.2 - $48.43 an hourExpandApply NowActive JobUpdated 0 days ago - UpvoteDownvoteShare Job
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Certificates and Licenses: Valid certification from the National Board for Certification of Occupational Therapy (NBCOT) Valid Occupational Therapist state license (where applicable) Interested in learning about us or other opportunities.
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As a Clinical Research Coordinator III, you will work independently providing study coordination including screening of potential research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
$71,219 - $121,000 a yearExpandApply NowActive JobUpdated 1 days ago
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