Clinical Data Jobs in Quebec (NOW HIRING)

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 a la fonction des operations d'essais cliniques en travaillant de maniere collaborative afin de fournir des resultats de haute qualite dans le cadre de nos programmes cliniques. Il s'agit d'un programme dedie sponsorise, axe sur le suivi d'etudes en oncologie dans l'Ouest canadien.

Vos responsabilites :

Votre role consistera a assurer le suivi des essais cliniques selon des standards eleves, en collaboration etroite avec votre equipe et les parties prenantes.

Principales responsabilites :

• Travailler de maniere autonome et proactive pour coordonner toutes les activites liees a la mise en place et au suivi des etudes, rediger des rapports d'avancement precis et maintenir la documentation des etudes.
• Gerer efficacement les demandes (queries) emises par le sponsor et etre responsable de l'optimisation des couts des etudes ; participer egalement a la preparation et a la revue de la documentation des etudes ainsi qu'aux etudes de faisabilite pour de nouvelles propositions, si necessaire.
• Developper et maintenir des relations solides et collaboratives avec les parties prenantes cles, les investigateurs cliniques et le personnel des sites.
• Garantir la securite des patients en assurant la conformite avec les procedures d'ICON, les protocoles et les exigences reglementaires.

Votre profil :

Vous apporterez une experience pertinente en monitoring d'essais cliniques, ainsi que les qualifications et competences suivantes :

Qualifications et experience requises :

• Diplome universitaire en medecine, sciences ou equivalent
• Connaissance des directives ICH-GCP et capacite a examiner et evaluer des donnees medicales
• Excellentes competences en communication ecrite et orale en anglais
• Experience en monitoring d'etudes en oncologie
• Bonnes competences relationnelles permettant de traiter les demandes (queries) de maniere efficace et en temps opportun
• Disponibilite pour des deplacements professionnels frequents (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 requesthere.

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