Job Description
Senior CRA Western Canada- Remote
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 Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.
**What You Will Be Doing:**
+ Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
+ Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
+ Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
+ Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
+ Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
**Your Profile:**
+ Advanced degree in a relevant field such as life sciences, nursing, or medicine.
+ Oncology monitoring experience required
+ Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
+ Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
+ Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
+ Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
+ Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license
Nous recherchons actuellement un(e) **Attaché(e) de Recherche Clinique Senior (Senior CRA)** pour rejoindre notre équipe diversifiée et dynamique. En tant que Senior CRA chez **ICON Plc** , vous jouerez un rôle clé dans la supervision et la gestion des activités des essais cliniques afin de garantir qu’ils sont conduits conformément au protocole, aux exigences réglementaires et aux normes de l’industrie. Vous contribuerez au succès des essais cliniques en assurant l’intégrité des données, la sécurité des participants et la conformité tout au long du cycle de vie de l’étude.
**Vos missions :**
+ Assurer le monitoring des centres d’essais cliniques afin de garantir le respect des protocoles d’étude, des exigences réglementaires et des Bonnes Pratiques Cliniques (BPC/GCP).
+ Réaliser des visites de centres pour évaluer la performance des sites, résoudre les problématiques et apporter le support nécessaire à la bonne conduite des essais.
+ Collaborer avec les équipes transverses afin d’assurer une collecte et un reporting des données précis et dans les délais.
+ Fournir formation, accompagnement et support aux équipes des centres investigateurs ainsi qu’aux autres ARC afin de maintenir des standards élevés de conduite des essais cliniques.
+ Développer et maintenir des relations efficaces avec les équipes des centres et les parties prenantes afin de faciliter le bon déroulement des opérations cliniques.
**Votre profil :**
+ Diplôme universitaire avancé dans un domaine pertinent tel que les sciences de la vie, les soins infirmiers ou la médecine.
+ **Expérience requise en monitoring en oncologie.**
+ Solide expérience en tant qu’Attaché(e) de Recherche Clinique, avec une excellente connaissance des processus des essais cliniques et des exigences réglementaires.
+ Capacité démontrée à gérer simultanément plusieurs centres et projets, avec de fortes compétences organisationnelles et en résolution de problèmes.
+ Expertise en pratiques de monitoring, intégrité des données et gestion des centres, avec une maîtrise des outils et logiciels d’essais cliniques.
+ Excellentes compétences en communication, relations interpersonnelles et gestion des parties prenantes, avec la capacité d’influencer et de promouvoir la conformité dans un environnement complexe.
+ Disponibilité pour voyager au moins **60 % du temps** (déplacements nationaux et internationaux – avion et voiture) et détention d’un permis de conduire valide.
**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 (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON 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 or submit a request here (https://careers.iconplc.com/reasonable-accommodations)
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 (https://wd3.myworkday.com/icon/d/task/1422$1235.htmld) to apply
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 Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.
**What You Will Be Doing:**
+ Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
+ Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
+ Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
+ Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
+ Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
**Your Profile:**
+ Advanced degree in a relevant field such as life sciences, nursing, or medicine.
+ Oncology monitoring experience required
+ Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
+ Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
+ Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
+ Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
+ Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license
Nous recherchons actuellement un(e) **Attaché(e) de Recherche Clinique Senior (Senior CRA)** pour rejoindre notre équipe diversifiée et dynamique. En tant que Senior CRA chez **ICON Plc** , vous jouerez un rôle clé dans la supervision et la gestion des activités des essais cliniques afin de garantir qu’ils sont conduits conformément au protocole, aux exigences réglementaires et aux normes de l’industrie. Vous contribuerez au succès des essais cliniques en assurant l’intégrité des données, la sécurité des participants et la conformité tout au long du cycle de vie de l’étude.
**Vos missions :**
+ Assurer le monitoring des centres d’essais cliniques afin de garantir le respect des protocoles d’étude, des exigences réglementaires et des Bonnes Pratiques Cliniques (BPC/GCP).
+ Réaliser des visites de centres pour évaluer la performance des sites, résoudre les problématiques et apporter le support nécessaire à la bonne conduite des essais.
+ Collaborer avec les équipes transverses afin d’assurer une collecte et un reporting des données précis et dans les délais.
+ Fournir formation, accompagnement et support aux équipes des centres investigateurs ainsi qu’aux autres ARC afin de maintenir des standards élevés de conduite des essais cliniques.
+ Développer et maintenir des relations efficaces avec les équipes des centres et les parties prenantes afin de faciliter le bon déroulement des opérations cliniques.
**Votre profil :**
+ Diplôme universitaire avancé dans un domaine pertinent tel que les sciences de la vie, les soins infirmiers ou la médecine.
+ **Expérience requise en monitoring en oncologie.**
+ Solide expérience en tant qu’Attaché(e) de Recherche Clinique, avec une excellente connaissance des processus des essais cliniques et des exigences réglementaires.
+ Capacité démontrée à gérer simultanément plusieurs centres et projets, avec de fortes compétences organisationnelles et en résolution de problèmes.
+ Expertise en pratiques de monitoring, intégrité des données et gestion des centres, avec une maîtrise des outils et logiciels d’essais cliniques.
+ Excellentes compétences en communication, relations interpersonnelles et gestion des parties prenantes, avec la capacité d’influencer et de promouvoir la conformité dans un environnement complexe.
+ Disponibilité pour voyager au moins **60 % du temps** (déplacements nationaux et internationaux – avion et voiture) et détention d’un permis de conduire valide.
**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 (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON 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 or submit a request here (https://careers.iconplc.com/reasonable-accommodations)
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 (https://wd3.myworkday.com/icon/d/task/1422$1235.htmld) to apply
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