Clinical Research Coordinator - Wichita, KS

About the role

IQVIA is seeking a Clinical Research Coordinator (CRC) to support the successful execution of clinical research studies under the guidance of the Principal Investigator. This role is ideal for candidates with hands-on clinical research experience who are passionate about patient care, data quality, and advancing healthcare innovation.

Responsibilities

• Perform clinical procedures including ECGs, vital signs, specimen/sample collection, and other protocol-required activities.
• Carefully coordinate and support daily clinical trial activities in compliance with study protocols, GCP, and site procedures.
• Conduct patient chart reviews and prescreening activities to identify potentially eligible participants.
• Recruit, screen, schedule, and orient study participants while ensuring patient safety and a positive participant experience.
• Support patient visits and assist with study-related documentation and follow-up activities.
• Prepare study materials, maintain study supplies, and assist with equipment setup and logistical planning.
• Collect, review, and accurately document clinical data in Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems.
• Support EDC data entry, query resolution, and data quality review in collaboration with investigators, sponsors, and monitors.
• Respond to sponsor and monitor queries in a timely and accurate manner.
• Maintain confidentiality, regulatory compliance, and adherence to Health & Safety policies.
• Act as a patient advocate and contribute to a collaborative and professional research environment.

Qualifications

• Bachelor’s degree preferred, or an equivalent combination of education and relevant experience.
• Minimum of 1+ years of relevant clinical research experience.
• Working knowledge of clinical trials, GCP guidelines, and medical terminology.
• Experience with patient chart review and prescreening activities.
• Ability to support patient visits and study coordination activities in a clinical research environment.
• Experience with EDC systems, including data entry and query resolution.
• Strong attention to detail with excellent organizational and communication skills.
• Ability to build effective working relationships with patients, investigators, sponsors, and team members.