First seen by our source: 2 hours ago
Sr. Site Management Assoociate
@ ICON Strategic Solutions
Canada
SIGNALS
Overview
ICON Strategic Solutions is hiring a Senior Site Management Associate, a full-time role working in a sponsor-dedicated model on clinical trials. The work centres on site administration and logistics during enrollment and database lock, plus regulatory documentation and quality oversight. The posting requires a bachelor's degree, at least 2 years of clinical research experience, and French/English bilingualism.
Responsibilities:
- Serve as primary contact for site administration and logistics
- Support trial master file and inspection readiness
- Assist sites with sponsor systems and escalate issues
- Monitor documentation compliance with GCP and SOPs
- Prioritize workload around study milestones
Requirements summary:
- Bachelor's degree with at least 2 years of clinical research experience
- Knowledge of Good Documentation Practices
- Systems experience such as Veeva or TMF highly preferred
- Understanding of clinical development paradigm
- Bilingual French and English
Tools & skills
Source and dates
Source type not verified · apify-linkedin
- Employer posting date
- Not provided
- First seen by our source
- 2026-11-15
- Source record updated
- 2026-11-15
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Senior |
| Department | Business operations |
| Experience | 2+ years |
| Hours per week | 40 (estimated) |
| Work setting | Office, Home |
| Position | Mostly sitting |
| Physical demands | physical low · computer high |
| Languages | English, French |
| Education | Bachelor’s degree (required) |
| Perks mentioned | Flexible hours, Retirement plan, Wellness, Childcare |
Summary and details written by AI from the posting; the employer’s posting is the authority.
ICON Strategic Solutions
| Field | Value |
|---|---|
| Open jobs on Jobsy | 2 |
Job description
Sr. Site Management Associate (French Speaking)
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.
As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
What You Will Do
Clinical Trial Execution & Site Support
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
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, 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
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.
As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
What You Will Do
Clinical Trial Execution & Site Support
- Serve as the primary point of contact for site administration and logistical needs during enrollment and maintenance and Data Base Lock (DBL).
- Collaborate closely with PIs and study coordinators to troubleshoot technical and administrative activities and issues flagged directly or indirectly (e.g. through the Clinical Research Liaisons)
- Ensure timely site support and sustained engagement through consistent communication, proactive problem-solving, and appropriate follow-up.
- Track and monitor documentation and systems information to ensure compliance and quality standards are maintained.
- Support protocol amendment releases, mass mailings and communications and providing guidance and documentation as needed.
- Assist sites with navigation or troubleshooting of sponsor systems (e.g., IRT, EDC, eTMF, CTMS) and escalate complex issues to system Subject Matter Experts (SMEs).
- Support dissemination of training materials related to protocol changes, systems updates, or new tools introduced during enrollment/maintenance.
- Field questions and provide refresher guidance to sites on processes such as eCRF entries, IWRS use, SIP data entry.
- Support maintenance and update of the Trial Master File (TMF) with essential enrollment and maintenance documentation to ensure inspection readiness.
- Ensure documentation of patient-related activities, deviation handling, and site correspondence aligns with GCP and internal SOPs.
- Flag inconsistencies or delays in data entry, document completion, or other quality-related indicators for follow-up.
- Support sponsor audits and inspections by preparing and providing site interaction documentation as needed.
- Collaborate with monitors, CRLs, and cross-functional teams to identify unique and trending needs, operational risks, and site administrative feedback.
- Utilize internal tracking tools and systems to ensure real-time visibility into site status/compliance.
- Provide input into continuous improvement efforts by sharing insights and feedback from sites.
- Prioritize workload based on study milestones, enrollment timelines, and site needs.
- Design and implement solutions to create lasting fixes through automation, process change or quality improvements.
- Bachelor’s degree with at least 2 years of experience in clinical research
- Knowledge of Good Documentation Practices
- Systems experience (Veeva, TMF) highly preferred
- Understanding of the overall clinical development paradigm
- Must be bilingual: French/English
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 maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized 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, subsidized travel passes, health assessments, among others.
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, 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
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