Bilingual FR/EN Study Start-up CRA

ICON Strategic Solutions; Canada; On-site; CAD 70,000 - 95,000; Full time

Benefits offered by this job

Competitive base salary and incentives

Health and wellbeing programmes incl.医

Retirement and pension plans

Life insurance and disability coverage

Employee assistance programmes andWell

Learning and development opportunities

Job summary

ICON Strategic Solutions is seeking a CRA I in Canada to contribute to clinical trial operations. You will monitor studies, coordinate setup, and maintain documentation while working closely with teams and stakeholders to ensure high-quality outcomes.

Requirements include a university degree in medicine or science, knowledge of ICH-GCP, strong interpersonal skills, and travel willingness around 60%. Employment is contingent on legal work status in the country.

Qualifications

• Academic degree in medicine, science, or equivalent.
• Knowledge of ICH-GCP guidelines with ability to review medical data.
• Strong interpersonal skills to handle queries promptly.
• Willingness to travel approximately 60% of the time.

Responsibilities

• Coordinate all activities for setting up and monitoring a study, including reporting and documentation.
• Manage sponsor-generated queries and support study cost efficiency; assist in document prep and feasibility reviews.
• Build and maintain relationships with investigators, site staff, and stakeholders.
• Ensure patient safety by complying with ICON procedures, protocols, and regulatory requirements.

Skills

Good social skills

ICH-GCP knowledge

Medical data evaluation

Willingness to travel

Education

University degree in medicine/science or equivalent

Job description

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.

As a CRA I at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programmes.

What You Will Do:

Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

• Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
• Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
• Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
• Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.

Your Profile:

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.

Required qualifications and experience:

• University degree in medicine, science, or equivalent
• Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
• Good social skills enabling you to deal with queries in a timely manner
• 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.

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.