Part-Time Clinical Research Coordinator – Onsite Wyomissing

IQVIA Inc; Wyomissing (Berks County); On-site; USD 48,000 - 58,000; Part time

Job summary

IQVIA Inc. seeks a Clinical Research Coordinator to join our Wyomissing, PA team on-site for a 24-hour per week position.

The role involves hands-on clinical procedures, patient recruitment, data entry, and ensuring compliance with GCP and study protocols. The ideal candidate has a Bachelor’s degree (or equivalent experience) and at least 1 year in clinical research, with proficiency in EDC systems and data quality management.

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.
• 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 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

ECG procedures

Vital signs

Study coordination

Documentation & data quality

Communication

Education

Bachelor’s degree or equivalent

Tools

EDC systems

Job description

IQVIA Inc. seeks a Clinical Research Coordinator to join our Wyomissing, PA team on-site for a 24-hour per week position.

The role involves hands-on clinical procedures, patient recruitment, data entry, and ensuring compliance with GCP and study protocols. The ideal candidate has a Bachelor’s degree (or equivalent experience) and at least 1 year in clinical research, with proficiency in EDC systems and data quality management.