Conduct study visits according to the study protocol. Obtain informed consent; collect
medical history and medication inventory. Administer psychological questionnaires. Perform
research procedures and tests: For example, magnetic resonance imaging, cognitive testing,
and physical performance testing.
Coordinate day-to-day activities and ensure the compliance of specific research studies.
Contact and schedule research participants while observing study-imposed time windows. Track
all study-related activities and deviations. Develop and submit IRB and research billing
documents as necessary. Work closely with study Principal Investigators to determine study
participant eligibility. Follow up with the study medical director on any participant adverse events
(AEs) and serious adverse events (SAEs). Issue study documents as necessary and create and
maintain source documents. Ensure that the study documents are properly organized and
manage study data in REDCap.
Serve as a backup for master research participant schedule coordination, notification of
necessary parties, greeting, and check-in/check-out participants. May make reminder calls and
send reminder letters to study participants. Update participant tracking logs as needed. May
obtain quotes for equipment and place orders. Monitor levels of lab supplies and notify
necessary parties when levels are low. May perform phone screening and documentation, data
entry, and IRB-related clerical duties.
Oversee program assistants, OPS, Graduate Assistants, and students in their research related
activities. Assist with training recruits in research-related activities.
Other duties as assigned by CRO/ORA leadership.
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