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Clinical Research Coordinator

Lake Forest, IL, us💼 Full-time🗓 2026-10-01 → 2026-10-04

Core

Coordinate all aspects of clinical trials, provide direct patient care including investigational medication dispensation, and manage study logistics and data under Principal Investigator direction.

Role type

Clinical Research Coordinator

Builds

Clinical trial operations and patient care services

Domain

Healthcare / Clinical Research

Deliverable

physical/clinical work

Required skills

Clinical trial coordination, patient care, protocol adherence, adverse event reporting, data entry and verification, regulatory compliance (GCP), vendor coordination, IRB documentation support

Preferred skills

ACRP or SOCRA certification, 3-5 years clinical research experience

Technologies

Electronic Clinical Research Forms (CRFs), hospital information systems

Responsibilities

Facilitate and coordinate logistical aspects of study protocols; provide direct patient care and dispense investigational medications; attend investigator meetings and coordinate site visits; schedule and lead protocol meetings; obtain and document adverse event data; ensure accurate data entry into CRFs with source documentation verification; maintain research files and assist in IRB submission materials; train research staff on data collection and reporting.