Clinical Research Coordinator

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

Benefits:

• 401(k)
• Health insurance
• Paid time off

About the Role:

PREMIER PSYCHIATRY in Orland Park, IL is looking for a dedicated Clinical Research Coordinator to join our team! This is an exciting opportunity to play a pivotal role in advancing medical research while working alongside experienced healthcare professionals in a dynamic clinical environment.

Responsibilities:

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

Requirements:

• Bachelor's degree in life sciences, healthcare, or a related field preferred
• Prior experience in clinical research coordination or a clinical setting is a plus
• Familiarity with GCP, ICH guidelines, and IRB submission processes
• Strong attention to detail with excellent organizational and time-management skills
• Proficiency in electronic data capture (EDC) systems and medical record software
• Excellent written and verbal communication skills
• ACRP or SOCRA certification (CCRC/CCRP) is a plus

About Us:

PREMIER PSYCHIATRY is a trusted medical practice based in Orland Park, IL, committed to delivering exceptional patient care and contributing to the advancement of medical science. Our team is passionate about improving patient outcomes through innovative research and evidence-based medicine. We foster a collaborative and supportive work environment where every team member plays a meaningful role in our mission.