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Transcribes study data from source documents to sponsor designated case report forms or records data for remote data entry if applicable. Pharmacy Supervisor/ Clinical research coordinator.
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Under the supervision of ADRC principal investigator (Dr. Victor Henderson) and clinical coordinator, main duties include in-person and telephone recruitment of research participants; obtaining informed consent; scheduling and coordination of research participant visits; maintaining longitudinal contact with participants by phone, email and other means; data collection (particularly including psychometric data), scoring, and entry.
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The Clinical Research Coordinator screens, enrolls and follows study participants, conducts data collection and entry, performs noninvasive cardiovascular tests according to study protocols, and conducts small group coaching sessions.
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CRCs are responsible for assisting study start-up; recruiting, enrolling, and retaining participants in the study; performing study assessments and follow-ups; data entry and management; and facilitating community outreach and stakeholder engagement.
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The Clinical Research Coordinator will manage study activities, including study recruitment, scheduling, patient consent, data collection/entry, reporting, and participant survey follow-up.
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Essential Functions & Responsibilities: Performs protocol duties; screening potential research volunteers, vital signs, ECG collection, laboratory sample collection/processing data collection and electronic data entry, as needed.
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Description The clinical research coordinator A (CRC A) will be responsible for data entry, organizing, maintaining and assuring the accuracy of all study documentation. The coordinator will oversee one or more clinical trials ensuring that the integrity of the protocol is maintained, all data and queries are answered in a timely manner, appropriate AEs and SAEs are reported to the sponsor and IRB per protocol.
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Scope: Protocol implementation & coordination Data collection, entry, reconciliation Patient interaction, procedures, scheduling Regulatory compliance & reporting Audit preparation Process improvement Other related duties as required.
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Essential Job Duties:In collaboration with other members of the clinical research site teamwork to ensure the entry of clinical visit data in EDC and other clinical data software/systems.
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Job responsibilities will include recruitment of study participants, scheduling study visits, psychological testing of participants, conducting MRI experiments, data entry, and data processing and analysis.
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Evaluates eligibility of candidates for clinical research studies by reviewing protocol defined eligibility requirements and/or collecting pertinent data on potential candidates, verifying appropriateness of patients for entry to clinical trials, and assisting the other staff in determining eligibility of potential patients.
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May perform budget entry in ERMS. Utilizes and integrates data from multiple financial and clinical databases and software applications including: Compass, EPEX, Emory Express, DOCLink, ERMS, eIRB, GE Centricity, Health Quest, MicroStrategy, and OnCore.
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Responsible for subject recruitment (screening, consenting support and enrollment), follow-up, data management (entry and reporting), detailed record keeping, regulatory compliance, report writing, and correspondence with investigators, IRBs, sponsors, CRO's and regulatory authorities.
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Interpret patient clinical information from electronic medical records (EMRs) for participation qualification and data entry. Complete all clerical data entry associated with each case or as assigned.
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The Department of OBGYN has an exciting opportunity for a full-time Clinical Research Coordinator 1 to work in Miami, FL. The Clinical Research Coordinator 1 serves as an entry level clinical research professional that has a basic foundation in clinical research through assigned responsibilities in data management or implementing clinical research protocols.
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data entry jobs Title: clinical research in Phenix-city, Alabama
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