CareerPlan

Clinical Research Spec II

Wilmot, USFull-time2026-11-06 → 2026-11-10

Core

Coordinates enrollment and manages moderate-risk/moderately complex clinical research studies from initiation to close-out, ensuring participant safety and data integrity.

Role type

Mid-level clinical research coordinator (moderate complexity)

Builds

Clinical trials and research studies

Domain

Healthcare / Clinical Research

Required skills

Study coordination, participant recruitment, screening, data entry, adverse event reporting, regulatory compliance (GCP), quality checks, audit preparation

Preferred skills

MS Office proficiency, cultural competency, health literacy support, team collaboration

Responsibilities

Coordinate participant enrollment and recruitment; manage study timelines and schedules; enter and verify research data; document adverse events and deviations; prepare for internal and external audits; maintain study logs and records; communicate with research teams and sponsors.