Clinical Study Lead

Responsibilities

• Oversee vendors for budget and timeline adherence during trials
• Develop strong relationships with vendors and sites throughout the study phases
• Understand and maintain detailed knowledge of study protocols for training and improvement contributions
• Cook up tasks with sponsor roles for study site readiness, including material preparation and drug shipping
• Review monitoring reports and CRO deliverables for compliance and oversight
• Conduct periodic eTMF/TMF reviews for adherence to standards and regulations
• Rewire vendor service agreements, budgets, and timelines while ensuring performance meets expectations
• Support audit activities and maintain clinical trial registry updates

Qualifications

• Undergraduate degree in clinical, science, or health-related field; licensed healthcare professional (e.g., registered nurse) preferred
• 5 years of relevant experience in clinical trial management
• 3 years of experience specifically in managing clinical trials
• Fluent in English with proficiency in the language of the host country

Benefits

• Comprehensive health, dental, and vision coverage
• Retirement and pension plans available
• Life assurance and disability coverage included
• Access to employee assistance and wellbeing resources

Pay

$121,576 – $151,970 annually

Schedule

Remote - US based candidates only, no visa sponsorship available