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IQVIA · 4 days ago

Clinical Research Coordinator - Surprise. AZ

Surprise, AZ

Full-time

Onsite

Entry Level

$35/hr - $42/hr

1+ years exp

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. The Clinical Research Coordinator (CRC) will support clinical research studies, ensuring compliance with protocols and GCP while performing clinical procedures and managing volunteer recruitment.

AnalyticsHealth CareLife Science

No H1B

Responsibilities

Perform complex clinical procedures including ECG, spirometry, sample collection, phlebotomy, and vital signs

Coordinate clinical research studies while ensuring adherence to study protocols and Good Clinical Practice (GCP)

Prepare study materials, manage logistics, and support overall site operations

Recruit, pre-screen, and orient volunteers, including chart reviews, physician referrals, and community outreach

Communicate study details effectively to potential participants and assess patient eligibility based on inclusion/exclusion criteria

Collect, verify, and accurately document clinical data in case report forms (CRFs) and electronic CRFs (eCRFs), including corrections and query resolution

Assist with Investigator Site File maintenance and collaborate with investigators and monitors to resolve study-related issues

Maintain a safe environment for volunteers in alignment with Health & Safety policies

Qualification

Clinical research experienceGCP principlesPatient recruitmentMedical terminologyData entryRegulatory experienceCommunication skillsAttention to detail

Required

High School Diploma or equivalent education/experience

Working knowledge of clinical trials, GCP principles, and medical terminology

Strong attention to detail and ability to build effective working relationships

Preferred

Minimum 1 year of relevant clinical research experience

Experience supporting lead CRCs with patient visits, data entry, query resolution, and prescreening referrals

Experience in both research and clinical settings

Experience with patient recruitment and prescreening, strong communication skills to discuss study details with patients, familiarity with trial activities from start-up to close-out, and clinical knowledge to interpret inclusion/exclusion criteria

Regulatory experience is a plus