Posted 11 days ago
Clinical Associate
@ ICR Canada - CAN
Montréal, Quebec
Overview
ICON Canada is hiring a remote Clinical Associate in Montreal or Toronto to support clinical trial design, implementation and management. The role involves coordinating study activities, monitoring, documentation and close-out, with about 60% travel. The posting requires full fluency in French and English, a bachelor's degree and prior clinical research or healthcare experience.
Responsibilities:
- Assist planning, execution and monitoring of clinical trials
- Coordinate site initiation, patient recruitment and monitoring visits
- Collaborate with clinical operations, data management and biometrics
- Maintain study documentation and regulatory compliance
- Support study close-out, data cleaning and clinical study reports
Requirements summary:
- Full fluency in French and English, written and verbal
- Bachelor's degree in a relevant scientific or healthcare field
- Clinical research or healthcare experience, ideally pharma, biotech or CRO
- Strong organization and time management
- Excellent attention to detail and problem-solving
- Willingness to travel about 60%
Tools & skills
Benefits mentioned
Source and dates
Employer career site / ATS feed · workday
- Employer posting date
- 2026-10-26
- First seen by our source
- 2026-10-27
- Source record updated
- 2026-11-03
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Entry level |
| Department | Quality assurance |
| Hours per week | 40 (estimated) |
| Travel | air: moderate · ground: moderate |
| Work setting | Home, Client sites, Office |
| Position | Sitting and standing |
| Physical demands | physical low · computer high |
| Languages | English, French |
| Education | Bachelor’s degree (required) |
| Fields of study | Life sciences, Healthcare |
| Perks mentioned | Retirement plan, Performance bonus, Wellness, Paid training |
Summary and details written by AI from the posting; the employer’s posting is the authority.
ICR Canada - CAN
| Field | Value |
|---|---|
| Open jobs on Jobsy | 14 |
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Clinical Associate at ICON, you will support the design, implementation, and management of clinical trials, contributing to the advancement of innovative treatments and therapies.
What You Will Do:
You will contribute to clinical coordination activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
- Assist in the planning, execution, and monitoring of clinical trials, ensuring adherence to protocol requirements, regulatory guidelines, and industry standards.
- Coordinate study activities including site initiation, patient recruitment, data collection, and monitoring visits to ensure timely and accurate data collection and documentation.
- Collaborate with cross-functional teams including Clinical Operations, Data Management, and Biometrics to support the successful execution of clinical trials.
- Maintain comprehensive study documentation and records, ensuring compliance with applicable regulations and standard operating procedures.
- Support study close-out activities including data cleaning, analysis, and preparation of clinical study reports.
Your Profile:
You will bring relevant clinical coordination experience, along with the following qualifications and skills.
Required qualifications and experience:
- Full professional fluency in both French and English (written and verbal) is required.
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Previous experience in clinical research or healthcare, preferably within the pharmaceutical, biotechnology, or CRO industry.
- Strong organizational and time management skills, with the ability to prioritize tasks and manage competing priorities effectively.
- Excellent attention to detail and problem-solving abilities, with a commitment to ensuring data accuracy, integrity, and compliance.
- Effective communication and interpersonal skills, with the ability to collaborate cross-functionally and build strong relationships with study teams and clinical sites.
- Willingness to travel as required (approximately 60%)
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
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
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
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.
Are you a current ICON Employee? Please click here to apply
Journal
Only you can see this. Kept on this device, and in your account when you sign in.