Clinical Research Coordinator - Wichita, KS

IQVIA•Parsippany, NJ

1d•$35 - $42•Onsite

About The Position

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. The CRC will play a critical role in study coordination, patient engagement, clinical procedures, and data management while ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.

Requirements

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.

Nice To Haves

Bachelor’s degree preferred, or an equivalent combination of education and relevant experience.

Responsibilities

Perform clinical procedures including ECGs, vital signs, specimen/sample collection, and other protocol-required activities.
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.