Clinical Research Associate, Sponsor Dedicated Job at IQVIA, Lake, WV

  • IQVIA
  • Lake, WV

Job Description

Clinical Research Associate role supporting sponsor-dedicated monitoring activities across multiple U.S. sites. Responsible for site management, protocol compliance, data integrity oversight, and regulatory documentation in accordance with GCP and ICH guidelines.

Responsibilities

  • Conduct site monitoring visits including initiation, ongoing monitoring, and close-out activities per protocol and GCP
  • Develop and track subject recruitment plans with sites to meet enrollment targets
  • Deliver protocol training and maintain regular site communication to manage expectations and resolve issues
  • Monitor study data quality, protocol adherence, and regulatory compliance; escalate concerns as needed
  • Track study progress including regulatory submissions, enrollment, CRF completion, and data queries

Requirements

  • Bachelor's degree in scientific or healthcare discipline preferred
  • At least 2 years independent on-site monitoring experience as CRA
  • Strong knowledge of GCP and ICH regulatory requirements
  • Proficiency with EDC, CTMS, eTMF, IVRS/IWRS systems
  • Advanced Microsoft Office skills (Word, Excel, PowerPoint)
  • Excellent written and verbal English communication abilities
  • Strong organizational, problem-solving, and time management skills

Compensation: $74,500–$197,500 base (annualized)

Job Tags

Work at office

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