Clinical Research Associate - Sponsor Dedicated Job at IQVIA, Carlsbad, CA

  • IQVIA
  • Carlsbad, CA

Job Description

Clinical Research Associate position focused on sponsor-dedicated monitoring and site management for clinical trials. Responsible for conducting site visits, managing recruitment, ensuring protocol compliance, and maintaining regulatory documentation across multiple study sites.

Responsibilities

  • Conduct site monitoring visits including initiation, ongoing monitoring, and closeout activities
  • Develop and track subject recruitment plans with study sites to meet enrollment targets
  • Provide protocol training and maintain communication with assigned sites
  • Evaluate study site compliance with protocol requirements and applicable regulations
  • Track study progress including regulatory submissions, enrollment metrics, CRF completion, and data queries

Requirements

  • Bachelor's degree in scientific or healthcare discipline preferred
  • Minimum 1.5 years of on-site clinical trial monitoring experience
  • Knowledge of Good Clinical Practice and ICH guidelines
  • Proficiency with Microsoft Office Suite and standard computer platforms
  • Strong written and verbal English communication skills
  • Organizational and problem-solving abilities
  • Ability to build effective working relationships with diverse stakeholders

Compensation: $90,200–$190,000 base

Job Tags

Work at office

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