Senior Site Activation Manager (US/CANADA)

Senior Site Activation Manager role at a global CRO involving oversight of clinical trial site activation strategies, study start-up activities, and cross-functional collaboration. The position requires leadership experience in clinical operations and regulatory compliance across US and Canadian locations, with remote work option.

Responsibilities

• Lead study start-up and site activation activities as primary accountability holder for assigned projects
• Drive cross-functional collaboration to meet site activation milestones and deliverables on schedule and budget
• Manage site activation metrics, identify risks, and implement mitigation strategies
• Partner with project teams on site qualification, regulatory, and essential document collection activities
• Mentor Site Activation Managers and contribute to process improvements and SOP development

Requirements

• Bachelor's degree in medical, biological, physical, health, pharmacy, or related science field
• Seven or more years of CRO and/or pharmaceutical industry experience
• Strong knowledge of ICH GCP guidelines, FDA/EU Clinical Trials Directives, and regulatory requirements
• Demonstrated project management, leadership, and risk mitigation skills
• Experience with site activation processes, clinical project planning, and execution
• Excellent communication and cross-cultural stakeholder management abilities
• Proficiency in spoken and written English

Compensation: $107,000-$213,000 base