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 Feasibility Specialist at ICON, you will be responsible for evaluating and optimizing the feasibility of clinical trials, ensuring they are well-planned and positioned for success.
What You Will Do
You will lead on clinical research tasks requiring technical depth, with a focus on quality and continuous improvement.
Key Responsibilities Include
Conducting in-depth feasibility assessments for clinical trials, including evaluating site capabilities, resource availability, and potential risks.
Collaborating with clinical operations teams, project managers, and other stakeholders to gather and analyze data relevant to trial feasibility.
Preparing comprehensive feasibility reports and recommendations to support project planning and decision-making processes.
Analyzing historical data and site performance metrics to identify trends, opportunities, and challenges impacting trial feasibility.
Developing and maintaining strong relationships with key stakeholders, including clinical sites, investigators, and external partners.
Staying up-to-date with industry trends, regulatory requirements, and best practices related to clinical trial feasibility and planning.
Providing mentorship and guidance to junior feasibility team members and contributing to continuous improvement efforts within the team.
Your Profile
You will have a strong foundation in clinical research, with the experience to work independently and guide others.
Required Qualifications And Experience
Bachelor's degree in a relevant scientific discipline or healthcare-related field
Extensive experience in clinical trial feasibility assessments, with a deep understanding of clinical research processes and site management.