Local Trial Manager - Oncology-Solid Tumor/ Phase 1 - Remote/US

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 Local Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Within this program you will thrive within a fast-paced, dynamic study design. As we are fully embedded with this global pharmaceutical client, you will experience a true “one team” approach that provides limitless opportunity to develop through training, mentorship, and support from leadership. 

What Will You Be Doing

Working outsourced and fully dedicated to one of our global pharmaceutical clients, the Local Trial Manager is responsible for the successful management and execution of study activities at a country level. Collaborating with the wider global study team, the Local Trial Manager leads the local team of Site Managers and Clinical Trial Assistants in order to deliver quality data and trial documents that are compliant with protocol, ICH-GCP guidelines, Standard Operating Procedures and regulatory requirements.

Key Tasks Include (But Not Limited To):

• Managing the local team to meet recruitment targets
• The efficient management of local vendors
• Timely review of trip reports submitted by Site Managers
• Targeted and effective study team training
• Preparation for audits
• Development of local study tools and procedures
• Proactive risk management and budget forecasting
• Managing studies from feasibility through to database lock and close-out, the Local Trial Manager acts as the key local manager throughout the lifecycle of the project

What Do You Need to Have

• A minimum of a 4-year Bachelor’s degree or relevant clinical experience is required
• 2 years of local trial management or mutually agreed clinical trial experience.
• 1 - 3+ years of trial management experience.
• At least 2 years of Oncology (Solid Tumor) experience required
• Solid understanding of the drug development process including ICH/GCP and local regulatory requirements. 
• Solid communication and computer skills required. 
• Proficient in speaking and writing the country language and English language. 
• Good written and oral communication skills.
• Willingness to travel with occasional overnight stay away from home depending on the region. 
• Flexible mindset and ability to work at a fast pace within small exploratory study teams. 
• Ability to work on multiple trials in parallel in different disease areas.

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.