Clinical Research Associate

Job summary

Clinical Research Associate - Montreal, Canada - Diabetes and Obesity 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 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…

Job details

Clinical Research Associate - Montreal, Canada - Diabetes and Obesity 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 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. Key responsibilities include: 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. Required qualifications and experience: 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). 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 ICON is an award-winning workplace that enables you to make a difference to patients’ lives by being part of a world-class clinical research organisation that helps deliver new medicines & medical devices that are benefitting patients worldwide. You are also part of a diverse company that cares about our world and is dedicated to conducting business more sustainably and supporting the communities in which we live. If you’re as driven as we are, join us. You’ll be working in a great environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry. Didn’t find the role you were looking for? Even if the perfect role isn’t available right now, we’re always excited to connect with talented individuals. Register to our Talent Community to receive updates on roles that align with your career goals.

What you’ll do

The CRA II is responsible for conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. They collaborate with investigators to maintain high-quality clinical data and contribute to the preparation of study documentation.

Requirements

Candidates must have a bachelor's degree in a scientific or healthcare field and at least 2 years of experience as a Clinical Research Associate. In-depth knowledge of ICH-GCP guidelines and a willingness to travel approximately 60% of the time are required.

Benefits

• Competitive Base Salary • Performance Related Incentives • Medical Coverage • Dental Coverage • Vision Coverage • Retirement And Pension Plans • Life Assurance • Disability Coverage • Employee Assistance Programmes • Wellbeing Resources • Learning And Development Opportunities

Listed skills

• Dedicated · Preferred
• Collaboration · Preferred
• preparation · Preferred
• Organisation · Preferred
• Health · Preferred
• Compliance · Preferred
• Documentation · Preferred
• Communication · Preferred
• Assurance · Preferred
• Development · Preferred
• Communication Skills · Preferred
• Google Cloud · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

• Clinical Trial Monitoring
• Protocol Compliance
• Data Integrity
• Patient Safety
• ICH-GCP Guidelines
• Site Qualification
• Site Initiation
• Site Close-out
• Data Review
• Clinical Study Reports
• Communication Skills
• Organizational Skills