Clinical Research Associate
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 at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programs. This is a sponsor dedicated program focused on monitoring Oncology studies in Montreal.
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
Excellent written and verbal communication in English
Experience monitoring Oncology studies
Good social skills enabling you to deal with queries in a timely manner
Willingness to travel as required (approximately 60%)
En tant que CRA chez ICON, vous contribuerez à la fonction des opérations d’essais cliniques en travaillant de manière collaborative afin de fournir des résultats de haute qualité dans le cadre de nos programmes cliniques. Il s’agit d’un programme dédié sponsorisé, axé sur le suivi d’études en oncologie dans l’Ouest canadien.
Vos responsabilités :
Votre rôle consistera à assurer le suivi des essais cliniques selon des standards élevés, en collaboration étroite avec votre équipe et les parties prenantes.
Principales responsabilités :
Travailler de manière autonome et proactive pour coordonner toutes les activités liées à la mise en place et au suivi des études, rédiger des rapports d’avancement précis et maintenir la documentation des études.
Gérer efficacement les demandes (queries) émises par le sponsor et être responsable de l’optimisation des coûts des études ; participer également à la préparation et à la revue de la documentation des études ainsi qu’aux études de faisabilité pour de nouvelles propositions, si nécessaire.
Développer et maintenir des relations solides et collaboratives avec les parties prenantes clés, les investigateurs cliniques et le personnel des sites.
Garantir la sécurité des patients en assurant la conformité avec les procédures d’ICON, les protocoles et les exigences réglementaires.
Votre profil :
Vous apporterez une expérience pertinente en monitoring d’essais cliniques, ainsi que les qualifications et compétences suivantes :
Qualifications et expérience requises :
Diplôme universitaire en médecine, sciences ou équivalent
Connaissance des directives ICH-GCP et capacité à examiner et évaluer des données médicales
Excellentes compétences en communication écrite et orale en anglais
Expérience en monitoring d’études en oncologie
Bonnes compétences relationnelles permettant de traiter les demandes (queries) de manière efficace et en temps opportun
Disponibilité pour des déplacements professionnels fréquents (environ 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