ICON
Local Trial Manager – Canada
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.
What you will be doing:
Planning, managing and overseeing clinical study execution in accordance with global program strategy, through leadership of the cross‑functional Local Study Team (LST).
Supporting country‑level planning and ensuring the site plan is aligned with site‑level and country‑level expectations, including budgeting, timelines, and deliverables.
Contributing to programme‑specific metrics, monitoring study progress, milestones, and site performance against study‑level and country‑level accountability and reconciliation.
Monitoring and managing the clinical study against timelines, deliverables, and budget; identifying and mitigating risks to ensure study goals are met.
Providing operational oversight and ensuring compliance with local regulations, ethics, and sponsor requirements.
Working closely with CRA, Data Management, Biostatistics, and Medical teams to ensure study data quality and integrity.
Communicating study status to stakeholders and contributing to the continuous improvement of local trial processes.
Qualifications
Bachelor’s degree in a scientific or related field (or equivalent experience).
3 + years’ experience in clinical research, with 2 + years’ experience leading local or regional trials.
Strong knowledge of clinical trial regulations, GCP, and local regulatory requirements.
Excellent project management, communication, and stakeholder‑management skills.
Proficiency with Microsoft Office and clinical trial management systems.
Proactive, detail‑oriented, and able to operate in a fast‑paced environment.
Your profile
Doctorate degree OR
Master’s degree & 3 years of directly related experience OR
Bachelor’s degree & 5 years of directly related experience OR
Associate’s degree & 10 years of directly related experience
Minimum 2‑3 years’ experience of leading local/regional trials
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 a competitive salary, ICON offers a range of benefits designed to support your well‑being and work‑life balance. These include:
Various annual leave entitlements
Health insurance options tailored to you and your family’s needs
Competitive retirement planning
Global Employee Assistance Programme, LifeWorks – 24‑hour access to a global network of specialists
Life assurance
Optional benefits such as childcare vouchers, bike purchase schemes, discounted gym, and travel passes
Visit our careers site to read more about the benefits ICON offers.
At ICON, inclusion and 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.
#J-18808-Ljbffr
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.
What you will be doing:
Planning, managing and overseeing clinical study execution in accordance with global program strategy, through leadership of the cross‑functional Local Study Team (LST).
Supporting country‑level planning and ensuring the site plan is aligned with site‑level and country‑level expectations, including budgeting, timelines, and deliverables.
Contributing to programme‑specific metrics, monitoring study progress, milestones, and site performance against study‑level and country‑level accountability and reconciliation.
Monitoring and managing the clinical study against timelines, deliverables, and budget; identifying and mitigating risks to ensure study goals are met.
Providing operational oversight and ensuring compliance with local regulations, ethics, and sponsor requirements.
Working closely with CRA, Data Management, Biostatistics, and Medical teams to ensure study data quality and integrity.
Communicating study status to stakeholders and contributing to the continuous improvement of local trial processes.
Qualifications
Bachelor’s degree in a scientific or related field (or equivalent experience).
3 + years’ experience in clinical research, with 2 + years’ experience leading local or regional trials.
Strong knowledge of clinical trial regulations, GCP, and local regulatory requirements.
Excellent project management, communication, and stakeholder‑management skills.
Proficiency with Microsoft Office and clinical trial management systems.
Proactive, detail‑oriented, and able to operate in a fast‑paced environment.
Your profile
Doctorate degree OR
Master’s degree & 3 years of directly related experience OR
Bachelor’s degree & 5 years of directly related experience OR
Associate’s degree & 10 years of directly related experience
Minimum 2‑3 years’ experience of leading local/regional trials
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 a competitive salary, ICON offers a range of benefits designed to support your well‑being and work‑life balance. These include:
Various annual leave entitlements
Health insurance options tailored to you and your family’s needs
Competitive retirement planning
Global Employee Assistance Programme, LifeWorks – 24‑hour access to a global network of specialists
Life assurance
Optional benefits such as childcare vouchers, bike purchase schemes, discounted gym, and travel passes
Visit our careers site to read more about the benefits ICON offers.
At ICON, inclusion and 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.
#J-18808-Ljbffr