On-Site CRC for Clinical Trials — ECG, Data, 24 hrs/wk

IQVIA Argentina

Boston (MA)

On-site

USD 48,000 - 58,000

Part time

4 days ago

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Job summary

IQVIA Newton, MA seeks a Clinical Research Coordinator to support clinical studies under the supervision of a Principal Investigator. This on-site, part-time role (24 hours/week) involves hands-on procedures, patient recruitment, data collection, and ensuring adherence to GCP and study protocols.

Responsibilities include performing ECGs and vital signs, coordinating studies, preparing materials, and maintaining data quality.

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.
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.