(Senior) Clinical Research Associate
$90.2k - $175.1kIQVIA
IQVIA seeks a Clinical Research Associate to conduct site monitoring visits and ensure protocol compliance across clinical trials. The role involves managing investigative site relationships, tracking study progress, and collaborating with cross-functional teams to deliver high-quality research operations.
Responsibilities
- Conduct site monitoring visits including selection, initiation, routine, and close-out activities
- Develop and maintain strong relationships with investigative sites to drive performance and enrollment
- Monitor protocol compliance, data integrity, and study execution quality
- Identify operational risks, resolve issues, and escalate concerns appropriately
- Track regulatory approvals, enrollment metrics, and data quality across assigned studies
Requirements
- Bachelor's degree in life sciences, healthcare, or related field
- 1.5+ years of on-site clinical trial monitoring experience
- Understanding of GCP, ICH, and regulatory compliance requirements
- Strong communication and problem-solving abilities
- Ability to manage multiple priorities in fast-paced environment
Compensation: $90,200.00 - $175,100.00 base
Vacancy posted 12 days ago
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