Clinical Research Coordinator - Anniston, AL

IQVIA • Parsippany, NJ

6d • Onsite

About The Position

IQVIA is seeking a Clinical Research Coordinator (CRC) to support the execution of clinical research studies conducted under the supervision of a Principal Investigator. This role is ideal for a detail-oriented, patient-focused professional who thrives in a hands-on clinical setting and is experienced in study coordination, patient visits, and data quality.

Requirements

• Bachelor’s degree preferred or an equivalent combination of education and relevant experience
• Minimum of 1+ years of clinical research experience
• Ability to conduct patient chart review and prescreen subjects against inclusion/exclusion criteria
• Experience independently leading subject study visits
• Prior experience with EDC data entry and query resolution
• Working knowledge of clinical trial conduct, GCP principles, and medical terminology
• Strong attention to detail with the ability to establish effective working relationships

Responsibilities

• Perform clinical research procedures, including ECGs, vital signs, and biological sample collection
• Coordinate day-to-day clinical research activities in accordance with study protocols and GCP requirements
• Prepare study materials, set up equipment, and support logistical planning for research visits
• Recruit, screen, prescreen, and orient study participants while ensuring patient safety and protocol adherence
• Lead and conduct subject study visits in alignment with protocol and investigator oversight
• Accurately collect, review, and document clinical data in case report forms (CRFs) and EDC systems
• Collaborate with investigators, study monitors, and site staff to resolve queries and maintain data integrity
• Serve as a patient advocate and maintain a safe clinical environment consistent with Health & Safety policies

Benefits

• health and welfare and/or other benefits

What This Job Offers

• Job Type: Part-time
• Career Level: Mid Level
• Education Level: Associate degree