On-Site Clinical Research Coordinator (Part-Time, 24h)

Regulatory Jobs; Wyomissing (Berks County); Sur place; USD 48 000 - 58 000; Temps partiel

Résumé du poste

IQVIA is seeking a part-time Clinical Research Coordinator to join our on-site team in Wyomissing, PA. The role involves hands-on clinical procedures, patient recruitment, and study coordination under a principal investigator’s supervision.

The CRC will perform ECGs, collect samples, monitor vital signs, and ensure data is accurately entered into CRFs while upholding GCP standards. The position emphasizes patient safety, protocol adherence, and collaboration with monitors.

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.

Responsabilités

• 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.

Connaissances

Clinical trials knowledge

GCP guidelines

Data entry / EDC

Attention to detail

Teamwork / communication

Formation

Bachelor’s degree preferred

Outils

EDC systems

Description du poste

IQVIA is seeking a part-time Clinical Research Coordinator to join our on-site team in Wyomissing, PA. The role involves hands-on clinical procedures, patient recruitment, and study coordination under a principal investigator’s supervision.

The CRC will perform ECGs, collect samples, monitor vital signs, and ensure data is accurately entered into CRFs while upholding GCP standards. The position emphasizes patient safety, protocol adherence, and collaboration with monitors.