Onsite Clinical Research Coordinator — Cardio Trials

IQVIA; Linden (NJ); On-site; USD 48,000 - 58,000; Part time

Job summary

IQVIA is seeking a Clinical Research Coordinator to support clinical studies in Somerset, NJ. This on-site, part-time role involves hands-on clinical procedures, patient interaction, and diligent study coordination under a Principal Investigator.

The ideal candidate has 1+ year of clinical research experience, familiarity with GCP and regulatory processes, and experience with cardiovascular studies. Responsibilities include data entry into CRFs/EDC and coordinating study activities.

Qualifications

• Bachelor’s degree preferred, or an equivalent combination of education and relevant experience.
• Minimum of 1+ year of experience in clinical research or related healthcare setting.
• Working knowledge of clinical trials, GCP principles, and medical terminology.
• Experience conducting study visits, including patient education and chart review.
• Exposure to cardiovascular studies and related clinical procedures is preferred.
• Familiarity with maintaining regulatory binders, managing study supplies, and updating study portals.
• Strong attention to detail with the ability to build effective working relationships.
• Proficiency in EDC systems, accurate data entry, and query resolution.

Responsibilities

• Perform clinical procedures including ECGs, vital signs, and biological sample collection.
• Coordinate daily clinical research activities in compliance with study protocols and GCP guidelines.
• Prepare and maintain study materials, equipment, and documentation to support study conduct.
• Recruit, screen, consent, and orient study participants, ensuring a positive and safe patient experience throughout the trial.
• Accurately collect, document, and enter clinical data into CRFs and EDC systems.
• Collaborate with investigators, monitors, and study team members to resolve queries and maintain data quality.
• Serve as a patient advocate while maintaining a safe clinical environment in accordance with Health and Safety policies.

Skills

ECG procedures

GCP knowledge

EDC systems

Data entry

Patient interaction

Education

Bachelor's degree preferred

Tools

EDC systems

Job description

IQVIA is seeking a Clinical Research Coordinator to support clinical studies in Somerset, NJ. This on-site, part-time role involves hands-on clinical procedures, patient interaction, and diligent study coordination under a Principal Investigator.

The ideal candidate has 1+ year of clinical research experience, familiarity with GCP and regulatory processes, and experience with cardiovascular studies. Responsibilities include data entry into CRFs/EDC and coordinating study activities.