Key Skills

Job Description

Clinical Trial Management 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 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 You will manage day-to-day clinical trial management activities, supporting your team to deliver quality outcomes. Key Responsibilities Include Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards. Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures. Build and manage strong relationships with trial investigators and stakeholders. Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines. Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management. 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 University degree in medicine, science, or equivalent combination of education & experience Demonstrated ability to drive the clinical deliverables of a study Subject matter expertise in the designated therapeutic area Prior monitoring experience is preferred Willingness to travel as required (approximately 25%) What ICON Can Offer You Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Core Responsibilities

Manage clinical trial operations and all aspects of trial delivery, ensuring timelines, budgets, and quality standards are met. Coordinate with cross-functional teams, investigators, and stakeholders while ensuring regulatory and ethical compliance and addressing trial design, vendor, and risk decisions.

Requirements

Requires a university degree in medicine or science, or an equivalent combination of education and experience, along with demonstrated ability to drive clinical study deliverables. Candidates should have clinical trial management experience and expertise in the designated therapeutic area; prior monitoring experience is preferred, and travel of approximately 25% is required.

Benefits

• Annual Leave
• Health Insurance
• Retirement Planning
• Employee Assistance Programme
• Life Assurance
• Childcare Vouchers
• Bike Purchase Schemes
• Discounted Gym Memberships
• Subsidized Travel Passes
• Health Assessments