Clinical Research Coordinator - Psychiatry Trials

Pradeep Thapar MD SC; Orland Park (IL); On-site; USD 52,000 - 76,000; Full time

Benefits offered by this job

401(k)

Health insurance

Paid time off

Job summary

Premier Psychiatry in Orland Park, IL is seeking a dedicated Clinical Research Coordinator to join our team. You will coordinate and manage day-to-day clinical trial operations, screen and enroll participants, and maintain accurate data in a fast-paced clinical setting.

Responsibilities include ensuring IRB/GCP compliance, liaising with sponsors and investigators, and preparing regulatory documents and study amendments. A life sciences degree and familiarity with EDC are preferred.

Qualifications

• Bachelor's degree in life sciences, healthcare, or related field required or preferred.
• Familiarity with GCP, ICH guidelines, and IRB submission processes.
• Proficiency in electronic data capture (EDC) systems.

Responsibilities

• Coordinate and manage day-to-day clinical trial operations and study activities.
• Screen, enroll, and monitor participants per study protocols.
• Collect, record, and maintain accurate clinical data and documentation.
• Ensure compliance with IRB regulations, GCP guidelines, and FDA requirements.
• Serve as liaison between sponsors, investigators, and participants.
• Prepare and submit regulatory documents, reports, and amendments.
• Schedule and coordinate study visits and follow-ups.

Skills

GCP familiarity

ICH guidelines

IRB submission process

Attention to detail

EDC systems

Communication skills

ACRP or SOCRA certification

Education

Bachelor's degree in life sciences/healthcare

Job description

Premier Psychiatry in Orland Park, IL is seeking a dedicated Clinical Research Coordinator to join our team. You will coordinate and manage day-to-day clinical trial operations, screen and enroll participants, and maintain accurate data in a fast-paced clinical setting.

Responsibilities include ensuring IRB/GCP compliance, liaising with sponsors and investigators, and preparing regulatory documents and study amendments. A life sciences degree and familiarity with EDC are preferred.