Clinical Trial 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 Clinical Trial Manager. 

What you will be doing:

• Accountability for the performance of assigned protocols in a country in compliance with ICH/GCP and country regulations, client policies and procedures, quality standards, and adverse event reporting requirements internally and externally.
• To be the Country point of contact (POC) for assigned protocols and proactively drive/track execution and performance of deliverables/timelines/results to meet country commitments, requiring strong collaboration with local Country Operations roles.
• Forecasting country resource needs and serving local business needs (sign contracts, manage budgets as delegated).
• Responsibility for quality and compliance of assigned protocols in the country and oversee CRAs and/or CTAs and training compliance.
• Performing quality control visits, reviewing Monitoring Visits Reports, and escalating performance issues and training needs to functional vendor and internal management as needed.
• Responsibility for collaboration and relationship management with investigators for insourced and outsourced studies, with functional outsourcing vendors and other external partners.
• Overseeing country and site validations, site selection, and recruitment in assigned protocols.
• Responsibility for clinical trial education to sites and act as the country POC for programmatically outsourced trials for assigned protocols.
• Representing the client in Pharma industry issues and in seeking influence in external R&D environment.
• Collaborating internally with local Pharmacovigilance and Regulatory Affairs to align on key decisions in countries.
• Supporting local and regional strategy development consistent with long-term corporate needs in conjunction with Regional Operations.

You Are: 

• Proactive, collaborative, and innovative.
• Bachelor's Degree or higher required.
• A professional with Clinical Project Management or Clinical Research Management in a pharmaceutical company or global CRO with at least 3+ years of experience.
• Strong understanding of start-up activities, clinical trial planning, (site) management, and metrics.
• Strong experience in dermatology clinical trials.
• Strong communication and leadership skills.
• Ability to coordinate and lead local teams to high performance and to lead across several dimensions simultaneously.

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 maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, 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.