Experteer Overview In this Senior Clinical Trial Manager role, you lead clinical trial operations within a sponsor-dedicated model backed by ICON’s integral expertise. You will drive cross-functional collaboration to deliver high-quality trial outcomes across programs. You will develop teams, optimize study management, and ensure timely start-up, enrollment, and oversight. This position offers the chance to impact patient care through scalable, globally coordinated trials and to grow with a leading FSP provider. Compensaciones / Beneficios • Oversee the clinical portion of the budget to ensure efficient resource allocation • Develop monitoring plans and tools to ensure effective study oversight • Train and mentor Clinical Research Associates (CRAs) to optimize performance • Drive enrollment and lead study start-up activities to meet timelines • Review trip reports and implement CAPA plans to maintain study integrity • Foster productive relationships with Sponsors, vendors,
and cross-functional teams Responsabilidades • 4+ years of experience in a Clinical Trial Management position at a CRO or Pharmaceutical Organization • Bachelor's degree in health, life sciences, or related field • 10+ years of relevant experience in clinical trial management • 2+ years of monitoring experience (preferred) • Experience in managing complex or global trials (advantageous) • Experience in managing all trial components from start-up to database lock (preferred) • Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives (preferred) • Willingness to travel approximately 25% Requisitos principales • Competitive base salary and incentives • Health and wellbeing programmes (medical, dental, vision) • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Learning and development opportunities