Clinical Research Coordinator - Ophthalmology
Core
Oversees details of clinical research studies, ensures compliance with study review boards, and monitors study execution in an ophthalmology setting.
Role type
Clinical Research Coordinator (Ophthalmology)
Builds
Clinical research studies for sponsors/CROs and Investigator Initiated Trials
Domain
Healthcare / Ophthalmology / Clinical Research
Deliverable
client delivery
Required skills
GCP guidelines knowledge, study protocol evaluation, patient recruitment and consent, adverse event reporting, regulatory document maintenance, study budget preparation, source documentation management, study drug/device accountability
Preferred skills
CCRC certification, ophthalmic technician experience, spreadsheet and word processing proficiency
Technologies
Word, Excel, Access
Responsibilities
Evaluate protocols and assist in study selection; prepare/manage site for clinical research studies; conduct in-services for study staff and review GCP guidelines; participate in subject recruitment and enrollment; maintain regulatory documents for study site and IRB; perform study-specific testing and administer questionnaires; complete case report forms and manage study supplies; assist in classifying and reporting Adverse Events; coordinate financial agreements and study budgets.
Seniority
Entry-level to Mid-level, hands-on IC
