Clinical Research Coordinator - Onsite Frisco TX

IQVIA; Parsippany-Troy Hills (NJ); On-site; USD 48,000 - 58,000; Full time

Job summary

IQVIA is seeking a Clinical Research Coordinator to join the team in Frisco, TX. This on-site role supports clinical studies under the supervision of a principal investigator, performing hands-on procedures and coordinating activities to ensure patient safety, protocol adherence, and high-quality data collection.

The position requires a Bachelor’s degree or equivalent experience, 1+ year in clinical research, familiarity with GCP and medical terms, and proficiency with EDC systems.

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

Data entry accuracy

Query management

Attention to detail

Relationship building

Education

Bachelor’s degree or equivalent

Tools

EDC systems

Job description

IQVIA is seeking a Clinical Research Coordinator to join the team in Frisco, TX. This on-site role supports clinical studies under the supervision of a principal investigator, performing hands-on procedures and coordinating activities to ensure patient safety, protocol adherence, and high-quality data collection.

The position requires a Bachelor’s degree or equivalent experience, 1+ year in clinical research, familiarity with GCP and medical terms, and proficiency with EDC systems.