On-Site Clinical Research Coordinator - 24hrs/Week

IQVIA LLC; Parsippany-Troy Hills (NJ); On-site; USD 4,822,000 - 6,017,000; Part time

Job summary

IQVIA is seeking a Clinical Research Coordinator to support on-site studies in Newton, MA. This part-time role involves hands-on clinical procedures, data collection, and strict adherence to GCP and study protocols.

Required: Bachelor's degree (or equivalent) and 1+ year in clinical research; familiarity with EDC, data entry, and CRF documentation. Join a leading global provider advancing healthcare and patient outcomes.

Qualifications

• Bachelor’s degree or equivalent education and experience.
• Minimum 1+ year of relevant clinical research experience.
• Working knowledge of clinical trials, GCP principles and medical terminology.
• Detail oriented with strong relationship-building skills.
• Proficiency with EDC systems and data entry accuracy.

Responsibilities

• Perform clinical procedures including ECG, sample collection and vital signs.
• Coordinate studies and ensure compliance with protocols and GCP.
• Prepare materials, set up equipment and plan study logistics.
• Recruit, screen and orient patients ensuring safety and well‑being.
• Record data in case report forms (CRFs) accurately.
• Collaborate with investigators and monitors to resolve queries and ensure data quality.
• Serve as patient advocate and maintain a safe environment per Health and Safety policies.

Skills

Bachelor's degree or equivalent

1+ year clinical research experience

GCP knowledge and medical terminology

Attention to detail and relationship‑m

EDC systems proficiency and data entry

Education

Bachelor's degree

Tools

EDC systems

Job description

IQVIA is seeking a Clinical Research Coordinator to support on-site studies in Newton, MA. This part-time role involves hands-on clinical procedures, data collection, and strict adherence to GCP and study protocols.

Required: Bachelor's degree (or equivalent) and 1+ year in clinical research; familiarity with EDC, data entry, and CRF documentation. Join a leading global provider advancing healthcare and patient outcomes.