On-Site CRC | 24h/Week | Patient-Focused Trials

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

Job summary

IQVIA is seeking a Clinical Research Coordinator (CRC) to join our team in Wyomissing, PA, supporting clinical research studies under the supervision of a principal investigator. This on-site role involves hands‑on procedures, patient recruitment, data collection, and ensuring compliance with GCP and study protocols.

You will work with investigators and monitors, perform ECGs, sample collection, vital signs, and manage study materials and logistics, while prioritizing patient safety and data

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.
• 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 knowledge

Clinical research familiarity

Attention to detail

Communication skills

Education

Bachelor’s degree or equivalent in a related field

Tools

EDC systems

Job description

IQVIA is seeking a Clinical Research Coordinator (CRC) to join our team in Wyomissing, PA, supporting clinical research studies under the supervision of a principal investigator. This on-site role involves hands‑on procedures, patient recruitment, data collection, and ensuring compliance with GCP and study protocols.

You will work with investigators and monitors, perform ECGs, sample collection, vital signs, and manage study materials and logistics, while prioritizing patient safety and data