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Description:
Coordinates clinical research studies on human subjects.
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.
Responsible for new research application (including study start-up processes and requirements) and submission of protocols with subsequent amendments. Participates in protocol writing as needed and maintains initial and continuing education for Good Clinical Practice compliance.
Skills:
Chart review, Clinical research, Pre-screening patients
Top Skills Details:
Chart review,Clinical research
Additional Skills & Qualifications:
AA/medical/technical school or 2 years of research and/or healthcare experience required
Knowledge, Skills, and Abilities
AA or medical/technical school preferred.
Bilingual in English/Spanish preferred.
Clinical research certification (CCRC, CCRP, CRA) and IATA certification preferred.
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Other
$58k-77k (estimate)
05/06/2023
04/28/2024
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