Part-Time Clinical Research Coordinator | On-Site, Frisco

IQVIA; Allen (TX); On-site; USD 48,000 - 58,000; Part time

Job summary

IQVIA in Frisco, TX is seeking a Clinical Research Coordinator to support clinical studies under the supervision of a principal investigator. This on-site, part-time role involves hands-on procedures, coordination, and ensuring adherence to protocol and GCP standards.

Responsibilities include performing ECGs, sample collection, patient recruitment and screening, data entry into CRFs, and collaborating with study monitors to maintain data quality and patient safety.

Qualifications

• Bachelor’s degree preferred or equivalent combination of education and relevant experience.
• Minimum 1+ years of relevant work experience in clinical research.
• Working knowledge of clinical trials, GCP principles, and medical terminology.
• Strong attention to detail and ability to establish effective working relationships.
• Proficiency with EDC systems , data entry accuracy, and query management.

Responsibilities

• Perform a variety of clinical procedures, including ECG, sample collection, and vital signs.
• Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.
• Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.
• Recruit, screen, and orient patients, ensuring their safety and well‑being throughout the study.
• Collect and accurately record clinical data in case report forms (CRFs).
• Collaborate with investigators and monitors, addressing queries and ensuring data quality.
• Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.

Skills

GCP principles

EDC systems

Data entry accuracy

Medical terminology

Attention to detail

Teamwork

Education

Bachelor’s degree or equivalent

Job description

IQVIA in Frisco, TX is seeking a Clinical Research Coordinator to support clinical studies under the supervision of a principal investigator. This on-site, part-time role involves hands-on procedures, coordination, and ensuring adherence to protocol and GCP standards.

Responsibilities include performing ECGs, sample collection, patient recruitment and screening, data entry into CRFs, and collaborating with study monitors to maintain data quality and patient safety.