Clinical Associate (French Speaking)

Clinical Associate - Hybrid Role - French Speaking - Toronto, Canada 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 Bilingual 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

The Clinical Associate will assist in the planning, execution, and monitoring of clinical trials while ensuring adherence to regulatory guidelines and protocol requirements. They will coordinate study activities, manage data collection, and collaborate with cross-functional teams to support successful trial execution.

Candidates must possess a bachelor's degree in a scientific or healthcare-related field and have previous experience in clinical research or the pharmaceutical industry. Full professional fluency in both French and English is required, along with strong organizational and communication skills.

• Competitive base salary • Performance related incentives • Medical coverage • Dental coverage • Vision coverage • Retirement plans • Pension plans • Life assurance • Disability coverage • Employee assistance programmes • Wellbeing resources • Learning and development opportunities

• Gestion du tempsSouhaitée
• Résolution de problèmesSouhaitée
• Souci du détailSouhaitée
• CommunicationSouhaitée

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• Clinical coordination
• French language
• English language
• Clinical research
• Regulatory compliance
• Data collection
• Study documentation
• Site initiation
• Patient recruitment
• Time management
• Problem-solving
• Communication
• Cross-functional collaboration
• Attention to detail
• Industry Standards
• Effective Communication
• Bilingual (French/English)
• Planning
• Multilingualism
• Biotechnology
• Management
• Clinical Research
• Clinical Trials
• Clinical Study Reports
• Data Cleansing
• Data Collection
• Data Management
• French Language
• Standard Operating Procedure
• Innovation
• Interpersonal Communications
• Problem Solving
• Operations
• Pharmaceuticals
• Time Management
• Collaboration
• Coordinating
• Prioritization
• Detail Oriented

• Healthcare
• Science & Research
• Administrative
• Clinical Associate
• Clinical Research Associate
• Biologists, Botanists, Zoologists and Related Professionals
• Clinical Research Coordinators
• Natural Sciences Managers

Formation minimale

Baccalauréat

Expérience minimale

2+ ans

Langue de l’offre

anglais

Heures de travail

40 heures par semaine