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 be doing:
Trial and site administration:

Tracking (e.g. essential documents) and reporting [e.g, Safety Reports)

Ensure collation and distribution of study tools and documents

Update clinical trial databases (CTMS) and trackers

Clinical supply & non-clinical supply management, in Collaboration with other country roles

Manage Labeling requirements and coordinate/sign translation change request

Document management:

Prepare documents and correspondence

Collate, distribute/ship, and archive clinical documents

Assist with eTMF reconciliation

Updating manuals/documents (e.g., patient diaries, instructions)

Document proper destruction of clinical supplies.

Prepare Investigator trial file binders

Execute eTMF Quality Control Plan

Obtain translations of documents

Regulatory & Site Start-Up responsibilities:

In a timely manner, provide to and collect from investigators forms/lists for site evaluation/validation, site start-up and submissions

Obtain, track and update study insurance certificates

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

Budgeting, Agreement and Payments: Collaborate with finance/budgeting representatives for

Develop country and site budgets (including Split site budget)

Tracking,



and reporting of negotiations

Maintenance of tracking tools

Contract development, negotiation, approval and maintenance (e.g. CTRAs)

Update and maintain contract; templates (in cooperation with Legal Department)

Payment calculation and execution (investigators, vendors, grants)

Ensure compliance with financial procedures

Monitor and track adherence and disclosures,

Budget closeout.

Meeting Planning:

Support local investigator meetings (invitations, prepare materials, select venue, support vendor where applicable)

What you need to have:

B.A./B.S. (Life Science preferred) or equivalent healthcare experience

Minimum 1-2 years in Clinical Research or relevant healthcare experience

Must have at least 2 years of budget negotiation experience.

Fluent in Local Languages and business proficient in English (verbal and written} and excellent communication skills

Must be bilingual in French

Good understanding of Global; Country/Regional Clinical Research Guidelines and ability to work within these guidelines.

Hands on knowledge of Good Documentation Practices

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.

ICH-GCP Knowledge appropriate to role

Effective time management, organizational and interpersonal skills,



conflict management

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

High sense of accountability/ urgency. Ability to set priorities and handle multiple tasks simultaneously in a changing environment

Works effectively in a matrix multicultural environment. Ability to establish and maintain culturally sensitive working relationships.

Demonstrates commitment to Customer focus.

Able to work independently

Proactive attitude to solving problems/ proposing solution

Must be able to go on site to sponsor office 2 days a week in Kirkland

Eligible to work in Canada without visa sponsorship

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives

Health and wellbeing programmes including medical, dental, and vision coverage where applicable

Retirement and pension plans

Life assurance and disability coverage

Employee assistance programmes and wellbeing resources

Learning and development opportunities through structured training and career pathways

Perks may vary depending on role and location.

Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

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📌 Bilingual Clinical Trial Coordinator - Finance - Montreal (Quebec City)
🏢 ICON Strategic Solutions
📍 Quebec City