Sr. CRA 1, IQVIA

IQVIA · Durham, NC +3 more

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Clinical OperationsFull-time$90k–$175kCompany career page

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Role summary

IQVIA seeks a Senior Clinical Research Associate with experience in therapeutic areas including oncology, cardiovascular, or metabolic disease. The role involves site monitoring, protocol management, and regulatory oversight for clinical trials across multiple locations.

What they're looking for

Bachelor's degree in scientific or healthcare discipline preferred
Minimum 2 years on-site clinical trial monitoring experience
Knowledge of GCP and ICH guidelines
Understanding of applicable clinical research regulatory requirements
Experience in oncology, cardiovascular, renal, metabolic, CNS, obesity, diabetes, GI, MASH/NASH, dermatology, or respiratory therapeutic areas

What you'll be doing

Conduct site monitoring visits including initiation, ongoing monitoring, and closeout activities per protocol and GCP standards
Develop and track subject recruitment plans with study sites to meet enrollment targets
Train assigned sites on protocol requirements and maintain regular communication regarding project expectations
Monitor study progress including regulatory submissions, enrollment metrics, CRF completion, and data query resolution
Maintain trial documentation including site files and investigator files in compliance with regulatory requirements

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