Clinical Research Associate - Sponsor Dedicated

2 years of independent on-site monitoring experience

Knowledge of therapeutic areas and clinical trial protocols gained through industry experience and training.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

Conduct all phases of site monitoring activities, including site selection, initiation, routine monitoring, and close-out visits.

Evaluate site performance and ensure adherence to study protocols, GCP, ICH guidelines, and applicable regulatory requirements.

Partner with investigative sites to develop, implement, and track patient recruitment and retention strategies that support enrollment goals.

Identify, document, and escalate quality or compliance concerns while supporting timely resolution of issues.

Monitor study progress by tracking regulatory submissions, approvals, enrollment metrics, CRF completion, and data query resolution.

Ensure essential study documentation is complete, accurate, and maintained within the Trial Master File (TMF) and Investigator Site File (ISF).