Clinical Project Manager (CMC expertise)

IQVIA seeks a Clinical Project Manager to lead clinical trial delivery and study execution in Durham, North Carolina. The role involves managing cross-functional teams, ensuring regulatory compliance, and driving operational excellence to meet contractual milestones and customer satisfaction.

Responsibilities

• Execute and manage clinical studies or study portions per contract while optimizing speed, quality, and cost
• Lead cross-functional project teams and manage collaboration across internal groups and customer contacts
• Develop integrated study management plans and monitor progress against contractual milestones
• Identify and manage project risks, issues, and quality concerns with corrective and preventative actions
• Manage project financials, forecast opportunities to accelerate activities, and control scope changes

Requirements

• Bachelor's degree in life sciences or related field
• 8-10 years biopharmaceutical industry experience supporting product development
• Comprehensive knowledge of drug development across preclinical, clinical, CMC, and regulatory disciplines
• Strong clinical trial knowledge including ICH GCP and applicable regulations
• Excellent written and verbal communication with strong presentation skills
• Leadership experience managing cross-functional teams and external stakeholders
• Proficiency in Microsoft Office applications and clinical trial management software