Senior CRA

IQVIA seeks a Senior Clinical Research Associate to conduct site qualification, monitoring, and close-out activities for clinical trials across multiple therapeutic areas. The role combines embedded sponsor-level exposure with IQVIA's global infrastructure, requiring extensive on-site monitoring experience and strong GCP and regulatory knowledge.

Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits per protocol and regulatory guidelines
• Maintain investigational site standards for patient safety, data integrity, protocol compliance, and quality
• Build relationships with investigators and site personnel; provide training and ongoing support
• Monitor study progress including regulatory documentation, recruitment, data queries, and performance metrics
• Collaborate on patient recruitment and retention strategies; identify and escalate study risks and site issues

Requirements

• University degree in Life Sciences, Health Sciences, Nursing, Pharmacy, or related discipline
• Minimum 4 years on-site clinical trial monitoring experience in CRO, pharmaceutical, or biotech
• Strong knowledge of GCP, ICH guidelines, and applicable regulatory requirements
• Excellent communication, organizational, and stakeholder management skills
• Ability to manage multiple priorities and work independently within cross-functional teams
• Willingness to travel up to 40–60% within assigned region
• Right to work in UK and Ireland; visa sponsorship not available