Clinical Trial Manager II - Bulgaria, Romania, Poland, Spain, Czech Republic, Hungary - Sponsor Dedicated - General Study Management Experience is required
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 Clinical Trial Manager II at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies for one of our sponsor´s studies.
What You Will Do:
You will oversee clinical trial management workstreams, ensuring deliverables meet quality and timeline expectations.
Key responsibilities include:
- Collaborate with cross-functional teams to design and implement effective clinical trial enrollment Collaborating with cross-functional teams to develop and implement comprehensive clinical trial protocols.
- Overseeing and managing the day-to-day operations of clinical trials,
ensuring compliance with regulatory standards.
- Analyzing and interpreting clinical trial data, identifying trends, and providing insights to optimize study outcomes.
- Proactively addressing challenges and implementing effective solutions to ensure the successful execution of clinical trials.
- Communicating effectively with internal and external stakeholders to foster strong partnerships and facilitate smooth trial processes.
- Accountable for the following deliverables: Study Initiation Meeting
o Clinical Study Activity Plan
o Study Delivery Plan
o TMF Quality Strategy Document
o DCT Set Up
o Study Demographic and Diversity Plan
o Vendors Oversight Plan
o Results Dissemination Plan
o Investigator/CRA Meeting Set Up & associated training
o Expected Document List
o Recruitment Tracking
o Budget tracking eTMF filing and Vendor Set Up and Management
o Patient Engagement Activities
o CSDD KOM &
📌 Clinical Trial Manager II (España)
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📍 España