General Study Manager
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
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.
- Preferred: Experience in managing all trial components from start-up to database lock.
- Preferre
📌 Global Study Manager (España)
🏢 Icon
📍 España