Part-Time CRC: Drive Patient‑Centric Clinical Trials

Regulatory Toolkit; Brownsville (TX); On-site; USD 48,000 - 58,000; Part time

Job summary

IQVIA is seeking a Clinical Research Coordinator in Brownsville, TX to support clinical studies on-site with 16 hours/week. Responsibilities include ECGs, data entry, patient visits, and ensuring study compliance and data integrity.

The role requires 1+ years in clinical research, knowledge of GCP, and proficiency with EDC systems. Sponsorship is not provided. Base pay ranges hourly between $35 and $42, depending on qualifications.

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.
• Experience conducting patient study visits and participant-facing clinical research activities.
• Proficiency with EDC systems, including accurate data entry, query resolution, and data management processes.
• Strong attention to detail and ability to establish effective working relationships.

Responsibilities

• Perform a variety of clinical procedures, including ECGs, sample collection, and vital signs assessments.
• Coordinate clinical research studies and maintain compliance with study protocols and GCP guidelines.
• Conduct patient study visits and support participants throughout the research process, ensuring a positive study experience.
• Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.
• Recruit, screen, and orient patients, evaluating eligibility based on study inclusion and exclusion criteria.
• Collect, enter, and maintain accurate clinical data in CRFs and EDC systems.
• Assist with EDC query management and resolution, working closely with investigators and monitors to ensure data accuracy.
• Collaborate with investigators, sponsors, and study monitors to address study-related issues and maintain high standards of data integrity.

Education

Bachelor’s degree or equivalent combination of education and relevant experience

Tools

EDC systems

Job description

IQVIA is seeking a Clinical Research Coordinator in Brownsville, TX to support clinical studies on-site with 16 hours/week. Responsibilities include ECGs, data entry, patient visits, and ensuring study compliance and data integrity.

The role requires 1+ years in clinical research, knowledge of GCP, and proficiency with EDC systems. Sponsorship is not provided. Base pay ranges hourly between $35 and $42, depending on qualifications.