On-Site Clinical Research Coordinator — Part-Time (24h/wk)

Mass Digital Health; Northborough (MA); On-site; USD 48,000 - 58,000; Full time

Job summary

IQVIA in Newton, MA seeks a Clinical Research Coordinator to support clinical studies under a principal investigator. This on-site role involves hands-on procedures, patient safety, and strict adherence to GCP and study protocols.

Responsibilities include performing ECGs, vital signs, data collection in CRFs, material preparation, and coordinating with investigators. A Bachelor's degree is preferred and at least 1 year of clinical research experience is expected.

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 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

Attention to detail

Communication

Team collaboration

Education

Bachelor's degree preferred

Tools

EDC systems

Job description

IQVIA in Newton, MA seeks a Clinical Research Coordinator to support clinical studies under a principal investigator. This on-site role involves hands-on procedures, patient safety, and strict adherence to GCP and study protocols.

Responsibilities include performing ECGs, vital signs, data collection in CRFs, material preparation, and coordinating with investigators. A Bachelor's degree is preferred and at least 1 year of clinical research experience is expected.