(Senior) Clinical Research Associate
$90.2k - $175.1kIQVIA
IQVIA seeks a Clinical Research Associate to lead site monitoring activities and ensure protocol compliance across clinical trials. The role involves partnering with investigative sites and cross-functional teams to execute studies to GCP/ICH standards while managing regulatory approvals, enrollment tracking, and data quality.
Responsibilities
- Lead and execute site monitoring visits including selection, initiation, routine, and close-out activities
- Build and maintain strong relationships with investigative sites to drive performance and recruitment
- Ensure protocol compliance, data integrity, and high-quality study execution
- Track study progress including regulatory approvals, enrollment metrics, and data quality
- Identify risks, resolve issues, escalate concerns, and maintain accurate documentation
Requirements
- Bachelor's degree in life sciences, healthcare, or related field
- 1.5+ years 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 fast-paced environment
Compensation: $90,200-$175,100 base
Vacancy posted 5 days ago
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