Clinical Research Coordinator

Socket.dev; Orland Park (IL); On-site; USD 60,000 - 80,000; 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. This role offers the chance to advance medical research in a busy clinical setting, partnering with experienced healthcare professionals.

You will screen, enroll, and monitor participants, manage data, and ensure regulatory compliance across IRB and FDA guidelines while coordinating sponsor and investigator communications.

Qualifications

• Bachelor’s degree in life sciences, healthcare or related field.
• Experience in clinical research coordination or clinical settings preferred.
• Familiarity with GCP, ICH guidelines and IRB submission processes.

Responsibilities

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

Skills

Attention to detail

Organizational skills

Time management

Communication skills

Education

Bachelor's degree in life sciences

Tools

EDC systems

Medical record software

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 documentationEnsure 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.