Clinical Research Coordinator 1
Core
Entry-level clinical research professional managing data, protocols, and participant screening for clinical studies.
Role type
Entry-level Clinical Research Coordinator
Builds
Clinical research studies and data management
Domain
Healthcare / Clinical Research
Required skills
Data management, protocol implementation, chart review, participant screening, specimen collection, regulatory compliance, adverse event reporting, study binder maintenance, drug distribution, protocol amendment assistance, progress reporting, administrative support, cultural competency, bilingual communication (preferred)
Preferred skills
Bilingual in English and Spanish
Technologies
Clinical research equipment, study binders, regulatory databases
Responsibilities
Perform chart review and pre-screening for study participant eligibility; coordinate routine clinical study activities including data collection and maintenance; perform moderate to complex research tests and experiments; operate clinical research equipment and troubleshoot operational failures; observe and report adverse events; identify and report protocol deviations; maintain study-specific regulatory binders; distribute study drug materials; assist in implementing protocol amendments; monitor protocol implementation and study progress; assist in participant recruitment and retention; collect, process, and ship specimens; assist with study orientation and in-services; adhere to international, national, and local regulatory requirements.
Seniority
Entry-level, supervised IC