Description
Must be experienced but willing to train for a specific nature of our specialty research studies, and bilingual for patient interaction.
Desire active, hardworking individual willing to engage immediately in several active protocols.
Summary of Job Duties/Responsibilities:
Review assigned study protocols.
Attend investigator meetings, site invitation visits, and any CRO training sessions.
Maintain accurate and complete study records in accordance with FDA regulations, as well as CRO and IRB.
Ensure compliance with IRB status reports, regulatory binders, patient medical records, drug accountability logs, laboratory manuals, temperature logs.
Complete protocol related activities such as obtaining research subject informed consent, monitoring subject compliance, performing diagnostic test such as PFT, EKG, vital signs, collection of lab specimen, and other appropriate procedures.
Calling and following up with potential research patients to inform them about research studies and assess patient interest.
Communicating with the PI regarding study progress, any challenges that arise with patients and or study.
Other duties as assigned.
Job Type: part time
Pay: From $19.00 - $30 per hour based on experience.
Discussion
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