Research Assistant (Biggs Institute)
- Supports the investigative team in the planning, evaluation, implementation, and documentation of scientific research.
- Defines and manages project resource needs within specified timelines and budgets.
- Maintains research databases; prepares and submits individual study progress reports as needed.
- Actively recruits, screens, enrolls, and schedules participant for various industry-sponsored or investigator-initiated trials.
- Ensures compliance with all regulatory agencies and funding source, Maintenance of appropriate regulatory files in compliance with ICH/GCP.
- Coordinates the interim monitoring visits for source document verification as well as preparing/updating IRB submissions to central and local IRBs.
- Assists in conducting a variety of research projects of limited complexity, collecting, evaluating, and interpreting data
- Performs all other duties as assigned.
- Schedules, coordinates, confirms, and supervises study visits.
- Obtains informed consent of study participants and ensures participant understanding and assessing willingness to continue with the study at each visit.
- Completes screening procedures for the review of the investigative team, conducts study visits, collects and processes data collection, completes research related forms, completes electronic data entry, and maintains study subject data and upload of source documents for various clinical trials.
- Follow industry standards and safety regulations.
- Maintains excellent communication with the investigative team.
- High attention to detail and strong organizational skills.
- Excellent written and verbal communication skills.
- Ability to work well independently with research participants and staff with minimal supervision.
- Possess strong skills for multitasking, meeting competing deadlines, prioritizing and supporting the investigator team.
- Bachelor's degree in basic science is required.
- None required.
- Bilingual in English/Spanish.
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