Part-Time Onsite Clinical Research Coordinator (16 hrs/wk)

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

Job summary

IQVIA is seeking a part-time Clinical Research Coordinator for on-site work in Brownsville, TX. The role involves hands-on clinical procedures, patient visits, data management, and coordination of studies under supervision of the PI.

Requirements include a Bachelor’s degree (or equivalent) and 1+ year of clinical research experience, with proficiency in EDC systems and GCP principles. Not eligible for sponsorship. Salary is hourly with base range $35–$42.

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.
• Demonstrated ability to recruit and screen patients according to study eligibility criteria.
• 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 Good Clinical Practice (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 while ensuring their safety and well‑being throughout the study.
• Collect, enter, and maintain accurate clinical data in case report forms (CRFs) and Electronic Data Capture (EDC) systems.
• Assist with EDC query management and resolution, working closely with investigators and monitors to ensure data accuracy, completeness, and quality.
• Collaborate with investigators, sponsors, and study monitors to address study-related issues and maintain high standards of data integrity.
• Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.

Skills

ECG procedures

Vital signs

Patient recruitment

Data entry

EDC systems

GCP knowledge

Education

Bachelor’s degree

Tools

EDC software

Job description

IQVIA is seeking a part-time Clinical Research Coordinator for on-site work in Brownsville, TX. The role involves hands-on clinical procedures, patient visits, data management, and coordination of studies under supervision of the PI.

Requirements include a Bachelor’s degree (or equivalent) and 1+ year of clinical research experience, with proficiency in EDC systems and GCP principles. Not eligible for sponsorship. Salary is hourly with base range $35–$42.