Clinical Research Associate II: On-Site Monitoring Specialist

IQVIA is seeking a Clinical Research Associate II with independent on-site monitoring experience to join our team in Durham, North Carolina.

You will conduct visits, ensure GCP/ICH compliance, train sites, monitor enrollment and data, prepare reports, and collaborate with cross‑functional teams to keep studies on track. Experience in Immunology/GI, Dermatology, Women''s Health, Asthma/Respiratory, or Ophthalmology is a plus.

For the Clinical Research Associate II:
On-Site Monitoring Specialist position at Regulatory Toolkit, we are reviewing applications now.

We are currently recruiting a Clinical Research Associate II:
On-Site Monitoring Specialist for our team in Durham, NC, United States.

This is a strong opening to take on the Clinical Research Associate II:
On-Site Monitoring Specialist role at Regulatory Toolkit.

As a Clinical Research Associate II:
On-Site Monitoring Specialist, you will play an important part at Regulatory Toolkit in Durham, NC, United States.