Senior CRA
- Montreal
- Clinical Monitoring
- ICON Full Service & Corporate Support
- Hybrid: Office/Remote
TA Business Partner
- Full Service Division
About the role
This vacancy has now expired. Please see similar roles below...
Requirements:
- Must be fluent in both French and English
- Must be located in Quebec
- Must have 1+ years of independent monitoring experience as a CRA
At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.
Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.
As a Clinical Research Associate at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV, ensuring adherence to applicable regulations and principles of ICH-GCP.
The role:
• Independent, proactive work to set up and monitor studies, complete reports and maintain documentation
• Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions
• Balancing sponsor generated queries
• Taking responsibility for study cost efficiency
• Preparation and review of study documentation and feasibility studies for new proposals
• Potential to assist in training and mentoring fellow CRAs
You will need:
• 1+ years of monitoring experience in phase I-III trials as a CRA
• College degree in medicine, science, or equivalent
• Previous monitoring experience in medium-sized studies, including study start-up and close-out
• Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
• Excellent written and verbal communication
• Ability to work to tight deadlines
• Availability to travel least 60% of the time (international and domestic -fly and drive) and should possess a valid driving license
Benefits of Working in ICON:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and 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 through the form below.
ICON plc est un chef de file mondial en matière de soins de santé intelligents et de recherches cliniques. De la molécule au médicament, nous faisons progresser la recherche clinique en fournissant des services externalisés à des entreprises pharmaceutiques, biotechnologiques, de fabrication de dispositifs médicaux ainsi qu’à des organismes gouvernementaux et de santé publique.
Les patients étant au cœur de tout ce que nous faisons, nous contribuons à accélérer le développement de médicaments et de dispositifs qui sauve des vies et améliore la qualité de vie.
Nos employés constituent notre principal atout, ils sont l’essence de notre culture et le moteur de notre réussite. Les employés de ICON ont pour mission de réussir et sont passionnés, ce qui fait en sorte que ce que nous faisons, nous le faisons bien.
Poste – Assistant(e) de recherche clinique I
Travailler de façon indépendante et proactive pour coordonner toutes les activités nécessaires à la mise en place et à la surveillance d’une étude, remplir les rapports d’étape de manière exacte et tenir à jour la documentation liée à l’étude
Soumettre des protocoles, des documents de consentement pour approbation auprès des comités d’éthiques/comités d’éthique indépendants et aider à la préparation de demandes auprès des autorités réglementaires comme demandé
Participer à la préparation et à la révision de la documentation relative à l’étude et aux études de faisabilité pour les nouvelles propositions au besoin
Gérer les demandes provenant du promoteur de manière efficace et être responsable du rapport coût-efficacité de l’étude
En fonction de votre niveau d’expérience, vous pourriez aider à la formation et au mentorat d’ARC moins expérimentés et/ou gérer des ARC qui travaillent sur des projets internationaux
Exigences
Minimum de 12 mois d’expérience indépendante et active en surveillance sur le terrain – tous les types de visites.
Connaissance des lignes directrices ICH GCP et expertise pour examiner et évaluer des données médicales
Excellentes habiletés en communication et en relations interpersonnelles, tant à l’écrit qu’à l’oral, vous permettant de gérer les demandes en temps opportun
Capacité à produire un travail rigoureux dans des délais serrés et un environnement exigeant
Pourquoi vous joindre à nous?
Le développement continu est vital chez nous, et en tant qu’ARC I vous aurez l’occasion de progresser dans votre carrière avec la possibilité de travailler dans d’autres domaines reliés afin d’élargir votre gamme de compétences. Nos avantages sociaux sont concurrentiels, notre envergure est internationale et nous nous soucions sincèrement de nos employés et de leur réussite.
Avantages à travailler chez ICON
Notre réussite est tributaire de la connaissance, des capacités et de la qualité de nos employés. C’est la raison pour laquelle nous sommes engagés envers le perfectionnement de nos employés dans le cadre d’une culture d’apprentissage continue. Une culture où vous êtes stimulé(e) par un travail épanouissant et où chaque expérience contribue à votre perfectionnement professionnel.
Chez ICON, nous mettons l’accent à vous offrir une rémunération globale concurrentielle qui n’inclut pas uniquement un excellent niveau salarial de base, mais aussi un vaste éventail de programmes de paye variable et de programmes de reconnaissance. De plus, nos avantages sociaux, politiques de soutien et initiatives relatives au mieux-être de catégorie supérieure sont conçus pour répondre à vos besoins et à ceux de votre famille à toutes les étapes de votre carrière, dès aujourd’hui et dans l’avenir.
ICON, ainsi que ses filiales, est un employeur inclusif, souscrivant au principe de l’égalité d’accès à l’emploi et s’engage à offrir un milieu de travail sans discrimination et harcèlement. Tous les candidats qualifiés seront pris en considération de manière égale et sans égard à la race, la couleur, la religion, le sexe, l’orientation sexuelle, l’identité de genre, l’origine nationale, le handicap ou le statut d’ancien combattant.
Si, en raison d’un problème médical ou d’un handicap, vous avez besoin d’un accommodement raisonnable pour une partie quelconque du processus de candidature, ou afin d’accomplir les tâches essentielles d’un poste, veuillez nous le faire savoir en remplissant le formulaire ci-dessous.
Application process
Once you find a job opening that fits your skills and interests, you can create an account, apply and check back on the progress of your application or apply for other roles. Once your application has been received, a confirmation email will be sent to your email.
Remember: this is our first time meeting you. Read the job description and highlight on your CV those experiences that we should learn about.
One of our experienced recruiters will read your profile and determine if you're fit for the role and the company. We are aware of instances where fake recruitment text messages and emails that can appear to come from ICON have been received by individuals. Always delete suspicious text messages or emails. Never give out personal financial information.
Reasonable AccomodationsDay in the life
Teaser label
Our PeopleContent type
BlogsPublish date
08/29/2023
Summary
To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her
Teaser label
Our PeopleContent type
BlogsPublish date
05/23/2023
Summary
How to progress as a Clinical Research AssociateTo thrive as a Clinical Research Associate (CRA), it is imperative to cultivate a multifaceted skill set and demonstrate unwavering commitment to exce
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A Day In The LifeContent type
BlogsPublish date
04/05/2023
Summary
Senior Clinical Research Associate Suzaita Hipolito talks about the satisfaction gained from working in Clinical Research. “What would it look like to wake up every day feeling happy and fulfilled?
by
Suzaita Hipolito
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