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Sr Clinical Trial Manager - Von Willebrand Disease

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About this role

Job title: Sr Clinical Trial Manager - Von Willebrand Disease

About the Role

ICON is seeking a Senior Clinical Trial Manager specialized in Von Willebrand disease to lead operational trial implementation, timelines, budgets, and cross-functional coordination. The role serves as the primary liaison for internal stakeholders and vendors to drive high-quality study execution in hematology trials.

What You'll Do

  • Accountable to deliver trials on time, within budget, and with high quality.
  • Manage trial timelines, budgets, feasibility, country/site identification and selection, and vendor oversight.
  • Review monitoring reports and conduct co-monitoring visits as needed.
  • Develop and manage recruitment plans, risk mitigation, and contingencies.
  • Ensure set-up and maintenance of systems for planning, tracking progress, and generating management reports.
  • Manage clinical trial supply plans and oversee data review and discrepancy resolution.
  • Lead multidisciplinary trial teams and conduct study team meetings.
  • Act as primary contact for trial between Drug Development and other departments.
  • Ensure adherence to Good Clinical Practice and applicable regulations.
  • Monitor study safety and participate in safety monitoring activities.
  • Review CRO/third-party invoices for scope alignment and cost control.
  • Provide training to CRAs and third-party vendors on protocols and practices.
  • Drive process improvements to increase efficiency and study quality.

What We're Looking For

  • BS/BA degree or relevant science-focused degree.
  • Minimum 7 years of experience in the biopharmaceutical industry or clinical research managing global trials.
  • Ability to manage complex and/or large trials.
  • Non-malignant hematology experience with Von Willebrand disease.
  • Working knowledge of ICH GCP and regulatory requirements.
  • Ability to manage multiple priorities across protocols and therapeutic areas.
  • Demonstrated leadership and problem-solving skills.
  • Experience executing activities from initiation to clinical study report.
  • Strong teamwork skills in a multidisciplinary environment; flexible and adaptable.
  • Excellent planning, prioritization, problem-solving, organizational skills, and customer orientation.
  • Strong communication skills with a broad range of stakeholders.
  • Must be legally authorized to work in the United States without future visa sponsorship.

Nice to Have

  • Relevant domain experience is appreciated.

Compensation & Benefits

ICON offers a competitive salary and a range of benefits designed to support well-being and work-life balance, including:

  • Various annual leave entitlements
  • Health insurance offerings
  • Competitive retirement planning offerings
  • Global Employee Assistance Programme
  • Life assurance
  • Flexible country-specific optional benefits
  • Opportunities to work in a diverse and inclusive culture

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