Clinical Research Associate - Oncology - Montreal

Pharmaceutical Research Associates, Inc; Montreal; Remote; CAD 70,000 - 90,000; Full time

Job summary

A leading clinical research organization in Montreal is searching for a Clinical Research Associate to oversee oncology trials. This role involves providing mentorship, ensuring compliance with regulations, and developing documents for study initiatives. Candidates must be bilingual in French and English with at least 2 years of clinical trial experience. ICON offers a diverse environment with numerous benefits, including health insurance options and retirement planning.

Benefits

Various annual leave entitlements

Health insurance options

Retirement planning options

Global Employee Assistance Programme

Life assurance

Flexible country-specific benefits

Qualifications

• At least 2 years monitoring clinical trials experience.
• Deep understanding of GCP, ICH, and local regulations.
• Experience in oncology is an asset.

Responsibilities

• Oversee multiple oncology trials ensuring high-quality execution.
• Act as Lead Site Manager, training and guiding other Site Managers.
• Support budget development and contract negotiations.

Skills

Bilingual in French and English

Collaboration

Communication

Patient recruitment strategies

Risk-based monitoring approaches

Education

B.Sc. in Biological Sciences

R.N. or equivalent

Tools

CTMS

EDC

TMF

IWRS

Job description

Overview

ICON plc is a world-leading healthcare intelligence and clinical research organization. We foster an inclusive environment that drives innovation and excellence. Join us in shaping the future of clinical development as a Clinical Research Associate.

Responsibilities

What you will be doing:

• Oversee multiple oncology trials, ensuring high-quality execution
• Provide leadership and mentorship to junior team members
• Act as Lead Site Manager, training and guiding other Site Managers
• Develop study start-up documents, including SIV agendas
• Represent Site Managers and Lead Trial Managers in meetings
• Ensure site perspective is reflected in study documents
• Review reports for assigned sites
• Support budget development and contract negotiations
• Assist with ASV activities and ensure alignment with study objectives
• Maintain compliance with Metrics/KPIs as per QOP

Qualifications

• Remote position based in Montreal
• Bilingual in French and English
• B.Sc., R.N., or equivalent in Biological Sciences preferred
• At least 2 years monitoring clinical trials experience
• Experience in oncology is an asset
• Knowledge of risk-based monitoring approaches is an asset
• Proficiency in clinical trial systems (CTMS, EDC, TMF, IWRS)
• Ability to drive patient recruitment strategies
• Strong collaboration and communication skills
• Deep understanding of GCP, ICH, and local regulations
• Up to 50% regional travel required

What ICON can offer you:

We prioritize building a diverse culture that rewards performance and nurtures talent. Benefits include:

• Various annual leave entitlements
• Health insurance options
• Retirement planning options
• Global Employee Assistance Programme
• Life assurance
• Flexible country-specific benefits

Visit our website for more details: https://careers.iconplc.com/benefits

ICON values inclusion & belonging. We are committed to providing an accessible environment and equal employment opportunities. If accommodations are needed, please inform us through the provided link.