Clinical Research Associate

Clinical Research Associate - Montreal, Canada - Diabetes and Obesity

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your Profile:

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

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Strong organizational and communication skills, with attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.
• Willingness to travel as required (approximately 60%)

En tant que CRA II chez ICON

En tant que CRA II (Clinical Research Associate II) chez ICON, vous participerez à la conception et à l’analyse des essais cliniques, à l’interprétation de données médicales complexes et contribuerez à l’avancement de traitements et thérapies innovants.

Vos responsabilités

Vous contribuerez aux activités de suivi des essais cliniques, en assumant la responsabilité de vos livrables et en travaillant en étroite collaboration avec les différentes parties prenantes.

Vos principales responsabilités incluront :

• Réaliser les visites de sélection, d’initiation, de suivi et de clôture des centres participant aux essais cliniques.
• Veiller au respect du protocole, à l’intégrité des données et à la sécurité des patients tout au long de l’étude.
• Collaborer avec les investigateurs et les équipes des centres afin de garantir le bon déroulement des études.
• Effectuer la revue des données et la résolution des demandes de clarification (queries) afin de maintenir un haut niveau de qualité des données cliniques.
• Contribuer à la préparation et à la révision de la documentation d’étude, notamment les protocoles et les rapports d’étude clinique.

Votre profil

Vous possédez une expérience pertinente en monitoring d’essais cliniques ainsi que les qualifications et compétences suivantes.

Qualifications et expérience requises :

• Licence/Bachelor ou diplôme équivalent dans un domaine scientifique ou lié aux soins de santé.
• Minimum de 2 ans d’expérience en tant qu’Attaché(e) de Recherche Clinique (ARC/CRA).
• Excellente connaissance des processus d’essais cliniques, de la réglementation applicable et des Bonnes Pratiques Cliniques (ICH-GCP) .
• Solides compétences organisationnelles et de communication, avec un grand souci du détail.
• Capacité à travailler de manière autonome tout en collaborant efficacement dans un environnement dynamique et en constante évolution.
• Disponibilité pour des déplacements professionnels fréquents (environ 60 % du temps ).

What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply