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Clinical Research Associate Ii Oncology

2 weeks ago

Remote, Canada ICON Full time

As a
**Clinical Research Associate I or II,** you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

ICON ISS is searching for oncology focused, bilingual Clinical Research Associate I and/or II’s (CRA II / Field Monitor) in Montreal and Quebec City to work on complex and exciting trials for a major sponsor.

**Responsibilities**:

- Contribute to the identification of new sites for clinical trials
- Assume ambassadorial role to facilitate communication between sites and sponsor CPO to increase value proposition to investigators.
- Facilitate the preparation and collection of site and country level documents during all phases of the trial. Supports the Clinical Study Manager in the oversight of Country and Site Trial Master Files (TMF). During all phases of the trial ensure archiving per relevant SOP.
- Execute site initiation and training, generate initiation visit report.
- Implement complete site management including monitoring visits, regulatory assessment, drug supply management, etc. to ensure compliance with protocol, GCP, global and local regulations, global and local processes.
- Identify problems at sites; resolve issues and escalate as appropriate.
- Complete preparation and generation of visit monitoring reports as per relevant SOP.
- Review and manage data at site; resolve technical and content issues on a continuous basis in order to achieve timely database lock targets.
- Implement site close-out activities and generate site close-out report.
- Provide feedback on site performance for future trial site feasibility/selection
- Improve skills by timely completion performance of assigned global and local training.

**Responsabilités**:

- Contribuer à l’identification de nouveaux centres pour des études cliniques
- Assumer un rôle d’ambassadeur pour faciliter les communications entre les centres d’étude et le Directeur de l’expérience patient du promoteur, afin de rehausser la proposition de valeur aux chercheurs.
- Faciliter la préparation et la collecte des documents aux centres d’étude et à l’échelle du pays pendant toutes les phases d’étude. Soutenir le travail du gestionnaire de l’étude clinique pour la surveillance des fichiers maîtres de l’étude (FME) aux centres d’étude et à l’échelle du pays. Pendant toutes les phases d’étude, s’assurer que l’archivage est conforme aux procédures d’exploitation normalisées.
- Effectuer l’initiation des centres d’étude et la formation du personnel, rédiger le rapport de la visite d’initiation.
- Mettre en place la structure complète de gestion des centres d’étude, entre autres, les visites de surveillance, les évaluations réglementaires, la gestion de l’approvisionnement en médicaments, pour assurer la conformité au protocole, aux BPC, aux réglementations mondiales et locales, et aux processus mondiaux et locaux.
- Identifier les problèmes aux centres d’étude; résoudre les problèmes et les communiquer à un palier supérieur de la direction, le cas échéant.
- Effectuer la rédaction complète et la distribution des rapports sur les visites de surveillance, conformément aux procédures d’exploitation normalisées pertinentes.
- Examiner et gérer continuellement les données recueillies aux centres d’étude, afin de résoudre rapidement les problèmes techniques et de contenu pour atteindre les cibles de verrouillage de la base de données en temps opportun.
- Mettre en œuvre les activités de clôture des centres d’étude et rédiger le rapport de clôture des centres d’étude.

**Qualifications**
- Bachelor’s Degree or higher in life sciences or equivalent
- Minimum 2 - 4 years’ clinical site monitoring experience from CRO or Pharmaceutical company
- Comprehensive knowledge and understanding of ICH-GCP
- Bilingual (verbal and written) in English and French languages required
- Able and willing to travel up to 60% regionally (sites in Quebec City and Montreal)
- Able and willing to work on several protocols/therapy areas
- Experience in phase I-IV trials
- Working knowledge of Electronic Data Capture (preferred)
- Experience/working knowledge of the oncology disease area (preferred but not required)
- Experience of Centralized/Risk Based/Targeted monitoring (preferred)
- Experience of working within a metric based environment (preferred)
- Excellent attention to detail
- Highly developed time management and organizational skills
- Focused on meeting study deliverables/targets
- Flexible and willing to adapt to changing priorities/timelines
- Oncology experience required

**Compétences**
- Baccalauréat ou diplôme supérieur en sciences de la vie ou un équivalent
- Minimum de 2 à 4 ans d’expérience en surveillance de centres d’étude pour une entreprise de recherche contractuelle ou une société pharmaceutique
- Des connaissances et une compréhension approfondies des bonnes pr