On-Site Clinical Research Coordinator – 24 hrs/wk

IQVIA Argentina; Northborough (MA); On-site; USD 48,000 - 58,000; Part time

Job summary

IQVIA is seeking a part-time Clinical Research Coordinator to join our on-site team in Newton, MA, supporting clinical studies under the supervision of a principal investigator. The role involves hands-on procedures, community outreach, and ensuring high standards of care and compliance.

Your responsibilities include performing ECGs, collecting samples, recording vital signs, and maintaining data integrity in CRFs while upholding GCP guidelines and patient safety.

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 ECG, sample collection, and vital signs.
• Coordinate clinical research studies and maintain protocol compliance.
• Prepare study materials, set up equipment, and plan logistics.
• Recruit, screen, and orient patients for studies.
• Collect and record data in case report forms (CRFs).
• Collaborate with investigators and monitors to resolve data queries.
• Act as a patient advocate and ensure Health and Safety compliance.

Skills

GCP principles

Medical terminology

Attention to detail

Interpersonal skills

Education

Bachelor's degree preferred or equivalent experience

Tools

EDC systems

Job description

IQVIA is seeking a part-time Clinical Research Coordinator to join our on-site team in Newton, MA, supporting clinical studies under the supervision of a principal investigator. The role involves hands-on procedures, community outreach, and ensuring high standards of care and compliance.

Your responsibilities include performing ECGs, collecting samples, recording vital signs, and maintaining data integrity in CRFs while upholding GCP guidelines and patient safety.