Part-Time Clinical Research Coordinator — Onsite

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

Job summary

IQVIA in Union, SC seeks a Clinical Research Coordinator to support clinical studies under the supervision of a principal investigator. This on-site role involves hands-on procedures, patient outreach, and ensuring high standards of care and compliance.

Responsibilities include ECG, sample collection, vital signs, data entry into CRFs, and coordinating study materials and logistics. A Bachelor’s degree or equivalent, 1+ year of clinical research, knowledge of GCP and medical terminology, and

Qualifications

• Bachelor’s degree preferred or equivalent combination of education and relevant experience.
• Minimum 1+ year 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 conducts 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

EDC systems

Data entry accuracy

GCP principles

Clinical procedures

Medical terminology

Education

Bachelor’s degree or equivalent

Tools

CRF data entry tools

Job description

IQVIA in Union, SC seeks a Clinical Research Coordinator to support clinical studies under the supervision of a principal investigator. This on-site role involves hands-on procedures, patient outreach, and ensuring high standards of care and compliance.

Responsibilities include ECG, sample collection, vital signs, data entry into CRFs, and coordinating study materials and logistics. A Bachelor’s degree or equivalent, 1+ year of clinical research, knowledge of GCP and medical terminology, and