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CRA 2/Senior CRA

IQVIA

IQVIA

Pharmaceutical Research Industry

Gilbert, AZ - USA

Entry Level

Onsite

Experteer Overview

In this CRA role, you partner with investigative sites and cross-functional teams to execute high-quality clinical trials aligned with GCP/ICH standards. You drive site performance, data integrity, and patient-focused study delivery, while identifying risks and ensuring inspection readiness. You will collaborate across departments to support timely study milestones and regulatory compliance, contributing to IQVIA’s mission to advance clinical research and improve patient outcomes.

Compensation / Benefits

  • opportunities for growth and career development
  • health and welfare benefits
  • competitive base pay
  • incentive plans may be offered
  • dynamic, fast-paced environment

Responsibilities

  • Lead and execute site monitoring visits (selection, initiation, routine, close-out) per GCP/ICH guidelines
  • Build and maintain strong site relationships to improve performance, recruitment, and engagement
  • Ensure protocol adherence, data integrity, and high-quality study execution
  • Proactively identify risks, resolve issues, and escalate when needed
  • Track study progress including regulatory approvals, enrollment, and data quality
  • Maintain accurate documentation and contribute to inspection readiness
  • Collaborate with cross-functional teams to ensure successful study delivery

Key requirements

  • Bachelor's degree in life sciences, healthcare, or related field (or equivalent experience)
  • 1+ year of on-site monitoring experience
  • Solid understanding of GCP, ICH, and regulatory requirements
  • Strong communication, problem-solving, and organizational skills
  • Ability to manage multiple priorities in a fast-paced environment

Description

In this CRA role, you partner with investigative sites and cross-functional teams to execute high-quality clinical trials aligned with GCP/I…
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