Clinical Research Associate - Sponsor Dedicated Job at IQVIA, Tampa, FL

  • IQVIA
  • Tampa, FL

Job Description

IQVIA seeks Clinical Research Associates II and Senior Clinical Research Associates to oversee clinical trial sites nationwide across multiple therapeutic areas. The role involves site monitoring, protocol compliance, regulatory adherence, and cross-functional collaboration to support study execution and patient enrollment.

Responsibilities

  • Conduct site monitoring activities including selection, initiation, routine visits, and closeout
  • Evaluate site performance and ensure protocol adherence, GCP compliance, and regulatory requirements
  • Partner with sites to develop and implement patient recruitment and retention strategies
  • Deliver protocol training and maintain communication with site staff on study expectations
  • Prepare monitoring reports and ensure essential documentation is complete and accurate

Requirements

  • Bachelor's degree in Life Sciences, Healthcare, Nursing, or related field preferred
  • Minimum 2 years independent on-site monitoring experience in pharmaceutical, biotech, or CRO
  • Strong understanding of clinical research processes, GCP, and ICH guidelines
  • Proficiency with Microsoft Office and electronic data capture technologies
  • Excellent verbal and written communication skills with diverse stakeholders
  • Strong organizational and time management abilities in fast-paced environments

Compensation: $71,900.00 - $189,000.00 base

Job Tags

Work at office

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