Clinical Trial Associate

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global 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 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.
• Exceptional analytical skills, with the ability to interpret complex data and provide actionable insights.
• Strong organizational and project management skills, with experience in handling multiple feasibility projects simultaneously.
• Excellent communication and interpersonal skills, with the ability to build and maintain effective relationships with stakeholders at all levels.
• Proficiency in data analysis tools and software relevant to feasibility assessments and clinical research.
• Willingness to travel as required (approximately 15%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply