Clinical Research Coordinator 2
Core
Mid-level clinical research professional assisting in planning, coordinating, implementing, monitoring, and evaluating specific clinical research studies from initiation to close-out.
Role type
Intermediate Clinical Research Coordinator
Builds
Clinical research studies (single site, established procedures, industry sponsorship)
Domain
Healthcare / Clinical Research
Required skills
Participant recruitment and screening, study procedure execution, data collection and recording, specimen handling, adverse event monitoring, protocol amendment implementation, regulatory compliance, study binder maintenance, drug distribution, stakeholder communication, training coordination
Preferred skills
ACRP (CCRC/ACRP-CP) or SOCRA (CCRP) certification, knowledge of ICH GCP, IRB, FDA requirements, HIPAA/privacy, safety reporting obligations
Technologies
CITI certification (GCP and Human Subjects tracks), CTRS training record system
Responsibilities
Coordinate priorities, timelines, and communications across multiple assigned studies; serve as routine day-to-day contact for assigned studies; monitor protocol implementation and study progress; support sponsor monitoring visit preparation and follow-up; provide protocol-specific coaching and orientation to CRC 1 staff; escalate higher-risk or ambiguous matters per the CTRS Escalation and Decision Authority Matrix.
Seniority
Intermediate, hands-on IC (via careerplan.io/jobs/R100101603-clinical-research-coordinator-2-at-umiami)