CRA II or Senior CRA (French-speaking)
- Montreal
- Clinical Monitoring
- ICON Full Service & Corporate Support
- Hybrid: Office/Remote
TA Business Partner
- Full Service Division
About the role
CRA II or Senior CRA, French-Speaking
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.
We are currently seeking a CRA II or Senior Clinical Research Associate to join our diverse and dynamic team. As a CRA II or Senior Clinical Research Associate , 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. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results.
What You Will Be Doing:
- Working independently and actively to coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentation
- Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested
- Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required
- Balancing sponsor generated queries efficiently and responsible for study cost-effectiveness
- Dependent on level of experience you may assist in training and mentoring less expert CRA’s and/or lead CRA’s working on international projects
Your Profile:
- 12 + months of monitoring experience in phase I-III trials as a CRA
- Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data
- You will possess excellent written and verbal communication in English
- Ability to produce accurate work to tight deadlines within a pressurized environment
- Remote except for Monitoring in which you will travel as per next bullet
- You will be asked to travel at least 60% of the time (international and domestic -fly and drive) and should possess a valid driving license.
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 II
- 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 18 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.
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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.
ICON, including subsidiaries, 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, colour, 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
A better career. A better world. A better you.
Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more
Day 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
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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?
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Suzaita Hipolito
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