Job Description

IHCRA - Academie des ARC
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
IHCRA - CRA AcademyIHCRA - Academie des ARC
Are you ready to take the next step in your clinical research journey? At ICON plc, we're driven by a shared mission--to help shape the future of clinical development and improve patients' lives around the world.

Etes-vous pret a franchir une nouvelle etape dans votre parcours en recherche clinique ? Chez ICON plc, nous sommes animes par une mission commune : contribuer a faconner l'avenir du developpement clinique et ameliorer la vie des patients a travers le monde.
Through our CRA Academy Program, we offer aspiring Clinical Research professionals the opportunity to grow into a Clinical Research Associate (CRA) role. As an In-House Clinical Research Associate (IHCRA), you'll gain the experience, mentorship, and training needed to transition into an independent site monitoring CRA.

Grace a notre programme de l'Academie des ARC, nous offrons aux professionnels en devenir de la recherche clinique la possibilite d'evoluer vers un role d'Attache de Recherche Clinique (ARC). En tant qu'ARC en interne (IHCRA), vous acquerrez l'experience, le mentorat et la formation necessaires pour evoluer vers un poste d'ARC independant en charge du suivi des sites.
This is a home-based role that requires travel and offers exposure to world-class clinical operations, cutting-edge studies, and a collaborative team environment.

Ce poste est en teletravail, avec des deplacements requis, et offre une exposition a des operations cliniques de classe mondiale, des etudes de pointe et un environnement d'equipe collaboratif.
What You Will Be DoingVos missionsLearning ICON's SOPs, ICH-GCP guidelines, and global regulatory standards.
Apprendre les procedures operatoires standard (SOP) d'ICON, les lignes directrices ICH-GCP et les normes reglementaires mondiales.
Serving as the primary point of contact for study sites and investigators.
Etre le point de contact principal pour les sites d'etude et les investigateurs.
Supporting investigator recruitment and site management activities.
Soutenir le recrutement des investigateurs et les activites de gestion des sites.
Maintaining timelines and ensuring complete, accurate data entry in ICON systems.
Respecter les delais et assurer une saisie de donnees complete et precise dans les systemes ICON.
Managing communications with clinical sites regarding documentation, enrollment, and data queries.
Gerer les communications avec les sites cliniques concernant la documentation, l'inclusion des patients et les requetes de donnees.
Participating in study meetings, audits, and quality assurance activities.
Participer aux reunions d'etudes, aux audits et aux activites d'assurance qualite.
Building strong relationships with internal teams, sites, and sponsors and maintaining confidentiality.
Etablir des relations solides avec les equipes internes, les sites et les promoteurs, tout en respectant la confidentialite.
Traveling as needed to support on-site or remote study needs.
Voyager selon les besoins pour soutenir les etudes sur site ou a distance.
Other duties as assigned
Autres taches selon les besoins


Through the ICON CRA Academy, you'll participate in a structured program that combines:

Grace a l'Academie des ARC d'ICON, vous participerez a un programme structure qui combine :Virtual and instructor-led training
Formation virtuelle et dirigee par un formateur
Hands-on field experience
Experience pratique sur le terrain
Continuous mentorship and performance assessment
Accompagnement continu et evaluation de la performance


Upon successful completion, you'll be assessed for movement to a CRA I position, where you'll lead independent monitoring activities and play a key role in advancing clinical research globally.

A l'issue du programme, vous serez evalue pour passer au poste d'ARC I, ou vous menerez de maniere autonome les activites de monitoring et jouerez un role cle dans l'avancement de la recherche clinique a l'echelle mondiale.
Your ProfileVotre profilA bachelor's degree (or international equivalent) in a life science, health, or clinical field.
Diplome universitaire (ou equivalent international) en sciences de la vie, sante ou domaine clinique.
18+ months of experience as a Study Coordinator or Clinical Research Nurse.
Plus de 18 mois d'experience en tant que coordinateur d'etude ou infirmier(ere) en recherche clinique.
1+ years experience with Oncology trials preferred
Minimum 1 an d'experience dans des essais en oncologie (prefere)
At least 12 months of experience supporting clinical
Au moins 12 mois d'experience en soutien aux etudes cliniques
Strong understanding of ICH-GCP and local regulatory guidelines.
Solide comprehension des lignes directrices ICH-GCP et des reglementations locales.
Willingness and ability to travel 50-80% (drive and fly).
Volonte et capacite a voyager entre 50 et 80 % du temps (en voiture et en avion).
Ability to lift up to 25 lbs as needed.
Capacite a soulever jusqu'a 11 kg si necessaire.
Must be legally authorized to work in Canada (no visa sponsorship available now or in the future).
Doit etre legalement autorise a travailler au Canada (aucune possibilite de parrainage de visa, maintenant ou a l'avenir).


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, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others.
Visit our careers site 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
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.