Senior Clinical Trial Manager

Responsibilities:

• Manage day-to-day operational aspects of clinical trials, including CRO/vendor management, drug supply, and clinical sites.
• Oversee vendor performance, timelines, contracts, and budgets; lead or contribute to study management team meetings.
• Identify study risks, develop mitigation strategies, and oversee Trial Master File and essential documents.

Requirements:

• Bachelor's degree (scientific or healthcare preferred) and 8+ years of clinical research experience, including international experience.
• Proven ability to lead all aspects of a clinical trial independently and manage cross-functional teams.
• Excellent planning, organizational, and communication skills; self-motivated with problem-solving abilities.

Benefits:

• Generous vacation time and public holidays, volunteer days, and long-term incentive plans.
• Employee stock purchase plans, wellbeing benefits, fitness reimbursement, tuition sponsoring, and professional development plans.
• Equal opportunity employer with reasonable accommodations for disabilities and protected statuses.