Sr. CRA 1, IQVIA Job at IQVIA, Durham, NC

  • IQVIA
  • Durham, NC

Job Description

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.

Responsibilities

  • 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

Requirements

  • 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

Compensation: $90,200-$175,100 base

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