Job Description
Full job description
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
What you will be doing:
Oversee multiple oncology trials, ensuring high-quality execution
Provide leadership and mentorship to junior flex team members
Act as Lead SM, training and guiding other Site Managers on study protocols
Develop essential study start-up documents, including SIV agendas
Represent Site Managers and Lead Trial Managers (LTMs) in key meetings
Ensure the SM perspective is reflected in study documents like Monitoring Guidelines
Review reports (SQV, SMV, SCV) for sites assigned to other SMs within the same trial
Support country budget development and contract negotiations in collaboration with CCS colleagues
Assist with ASV activities and ensure alignment with study objectives
Maintain compliance with Metrics/KPIs as outlined in the Quality Oversight Plan (QOP)
You Are:
Remote position located in Edmonton, Canada
Minimum of a B.Sc., R.N., or equivalent degree, preferably in Biological Sciences
At least 2 years of experience monitoring clinical trials in the pharmaceutical industry
Experience in multiple therapeutic areas is an asset, particularly in oncology required
Knowledge of risk-based/analytical monitoring approaches is an asset
Proficiency in clinical trial systems such as CTMS, EDC, TMF, IWRS, and safety reporting tools
Ability to actively drive patient recruitment strategies at assigned sites
Strong collaboration with investigators and site staff to meet study timelines
Effective communication and influencing skills to manage study sites effectively, both remotely and in-person
Ability to work independently while being a strong collaborator
In-depth understanding of Good Clinical Practice (GCP), ICH guidelines, and local regulatory requirements
Up to 50% regional travel required
To qualify, applicants must be legally authorized to work in Canada, and should not require, now or in the future, sponsorship for employment visa status
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, 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, colour, religion, sex, ****** 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.
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
What you will be doing:
Oversee multiple oncology trials, ensuring high-quality execution
Provide leadership and mentorship to junior flex team members
Act as Lead SM, training and guiding other Site Managers on study protocols
Develop essential study start-up documents, including SIV agendas
Represent Site Managers and Lead Trial Managers (LTMs) in key meetings
Ensure the SM perspective is reflected in study documents like Monitoring Guidelines
Review reports (SQV, SMV, SCV) for sites assigned to other SMs within the same trial
Support country budget development and contract negotiations in collaboration with CCS colleagues
Assist with ASV activities and ensure alignment with study objectives
Maintain compliance with Metrics/KPIs as outlined in the Quality Oversight Plan (QOP)
You Are:
Remote position located in Edmonton, Canada
Minimum of a B.Sc., R.N., or equivalent degree, preferably in Biological Sciences
At least 2 years of experience monitoring clinical trials in the pharmaceutical industry
Experience in multiple therapeutic areas is an asset, particularly in oncology required
Knowledge of risk-based/analytical monitoring approaches is an asset
Proficiency in clinical trial systems such as CTMS, EDC, TMF, IWRS, and safety reporting tools
Ability to actively drive patient recruitment strategies at assigned sites
Strong collaboration with investigators and site staff to meet study timelines
Effective communication and influencing skills to manage study sites effectively, both remotely and in-person
Ability to work independently while being a strong collaborator
In-depth understanding of Good Clinical Practice (GCP), ICH guidelines, and local regulatory requirements
Up to 50% regional travel required
To qualify, applicants must be legally authorized to work in Canada, and should not require, now or in the future, sponsorship for employment visa status
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, 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, colour, religion, sex, ****** 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.
💡 Quick Summary
Seeking a career-building opportunity? The Clinical Research Associate - Cross TA - Edmonton position is now open for candidates interested in the Health Jobs sector. This role in Edmonton offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Health Jobs is a plus.
