Senior Clinical Trial Manager
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s general expertise.
As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
As a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes.
What You Will Do:
Your focus will be on coordinating clinical trial management delivery, resolving issues, and developing team capability.
Key responsibilities include:
- Budget Oversight Oversee the clinical portion of the budget to ensure efficient resource allocation.
- Ensuring Effective Study Oversight: Develop monitoring plans and tools, ensuring effective study oversight.
- Optimizing Performance: Train and mentor Clinical Research Associates (CRAs) to optimize their performance.
- Timely Study Start-Up & Enrollment: Drive enrollment and lead study start-up activities, adhering to timelines.
- Improving Study Integrity Review trip reports and implement corrective and preventative action plans when necessary.Building Productive Relationships: Foster productive relationships with Sponsors, vendors, and cross-functional teams.
Your Profile:
You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:
- 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 global trials is advantageous.