As a Clinical Trial Manager, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
To manage long-term strategic objectives including quality, timeliness, overall study performance and continuous process improvement in assigned clinical trials. LTM is responsible for all clinical trial activities within a country from study start up through final close out visit ensuring that organizational and regulatory requirements are met.

Responsibilities:

• Manage multiple complex tasks requiring independent decision-making
• Interact with Operations team leader to determine team requirements
• Develop country budget and timeline
• Supervise site/investigator selection process
• Monitor progress of clinical trial agreement negotiation within country
• Monitor site performance in relation to timeline
• Ultimately responsible for the quality and timeliness of country trial performance in assigned
• Phase 1-3 trials for project team
• Contribute towards recruitment strategy and contingency plan in partnership with other functional areas. Recommend implementation of contingency plan when necessary
• Life science degree
• At least 1 year of experience as Local Trial Manager or CTM (mandatory)
• Good interpersonal and organizational skills
• Ability to handle multiple priorities is essential

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
At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We’re proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. 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 through the form below.
https://careers.iconplc.com/reasonable-accommodations
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.

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• Manage multiple complex tasks requiring independent decision-making
• Interact with Operations team leader to determine team requirements
• Develop country budget and timeline
• Supervise site/investigator selection process
• Monitor progress of clinical trial agreement negotiation within country
• Monitor site performance in relation to timeline
• Ultimately responsible for the quality and timeliness of country trial performance in assigned
• Phase 1-3 trials for project team
• Contribute towards recruitment strategy and contingency plan in partnership with other functional areas. Recommend implementation of contingency plan when necessary
• Life science degree
• At least 1 year of experience as Local Trial Manager or CTM (mandatory)
• Good interpersonal and organizational skills
• Ability to handle multiple priorities is essentia