In this Senior Clinical Trial Manager role, you lead clinical trial operations within a sponsor-dedicated model backed by ICON’s global 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 / Incentivos
- 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
Responsabilidades
- 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
Requisitos principales
- 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%
- leadership and people development
- stakeholder management
- problem solving and issue resolution
- clinical trial management
- start-up to database lock
- monitoring practices