On-Site Clinical Research Coordinator — Part-Time (24h/wk)

3M HEALTHCARE; Anniston (AL); On-site; USD 48,216 - 57,859; Part time

Job summary

IQVIA in Anniston, AL is seeking a part-time Clinical Research Coordinator to support execution of clinical studies under PI supervision. On-site role with 24 hours weekly, involving patient visits, data collection, and regulatory compliance.

Responsibilities include coordinating visits, performing procedures, data entry into CRFs/EDC, and collaborating with investigators and staff to ensure patient safety and protocol adherence.

Qualifications

• 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

Skills

Clinical research experience

EDC data entry

GCP knowledge

Patient safety

Education

Bachelor’s degree preferred

Tools

EDC systems

Job description

IQVIA in Anniston, AL is seeking a part-time Clinical Research Coordinator to support execution of clinical studies under PI supervision. On-site role with 24 hours weekly, involving patient visits, data collection, and regulatory compliance.

Responsibilities include coordinating visits, performing procedures, data entry into CRFs/EDC, and collaborating with investigators and staff to ensure patient safety and protocol adherence.