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. Update clinical trial databases (CTMS) and trackers Trial and site administration In a timely manner, provide to and collect from investigators forms/lists for site evaluation/validation, site start-up and submissions Support preparation of submission package for IRB/ERC and support regulatory agencies submissions.

Publish study results for GCTO and RA where required per local legislation Collate, distribute/ship, and archive clinical documents Assist with eTMF reconciliation Execute eTMF Quality Control Plan Develop country and site budgets (including Split site budget) Contract development, negotiation, approval and maintenance (e.g. Update and maintain contract; templates (in cooperation with Legal Department) Support local investigator meetings (invitations, prepare materials, select venue, support vendor where applicable) Life Science preferred) or equivalent healthcare experience Minimum 1-2 years in Clinical Research or relevant healthcare experience Fluent in Local Languages and business proficient in English (verbal and written) and excellent communication skills Must be bilingual in French Country/Regional Clinical Research Guidelines and ability to work within these guidelines. Good IT skills (Use of MS office, use of some clinical IT applications on computer) and ability to adapt to new IT applications; Strong MS Excel skills required.

Effective communication with external customers (e.g. sites and investigators)



Demonstrates commitment to Customer focus. Must be able to go on site to sponsor office 2 days a week in Kirkland 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. 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 advantages, 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.

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. #

📌 Clinical Trial Coordinator - Finance - Montreal, Canada
🏢 ICON Strategic Solutions
📍 Montreal