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In this role you will lead clinical trial management activities within ICON's sponsor-dedicated model. You will guide cross-functional teams to deliver high-quality trial outcomes and oversee budget, start-up, and enrollment activities. You will develop team capability and foster strong relationships with sponsors and vendors. This is an opportunity to shape global trials and drive efficient, compliant operations in a leading FSP organization.
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 CRAs to optimize performance
- Drive enrollment and lead study start-up activities within timelines
- Review trip reports and implement corrective and preventative actions for study integrity
- Foster productive relationships with Sponsors, vendors,
and cross-functional teams
Responsabilidades
- A minimum of 4+ years of experience in a Clinical Trial Management position at a CRO or Pharmaceutical Organization
- Bachelor's degree in health, life sciences, or other relevant fields of study
- At least 10+ years of relevant experience in clinical trial management
- Preferred: 2+ years of monitoring experience
- Experience in managing complex or integral trials is advantageous
- Preferred: Experience in managing all trial xugodme components from start-up to database lock
- Preferred: Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives
- Willingness to travel as required (approximately 25%)
Requisitos principales
- annual leave entitlements
- health insurance offerings
- retirement planning offerings
- Global Employee Assistance Programme LifeWorks
- Life assurance
- flexible country-specific optional benefits