Infirmier(ère) autorisé(e) en essais cliniques - Registered Nurse - Clinical Trials

Infirmier(ère) autorisé(e) en essais cliniques - Registered Nurse - Clinical Trials

08 Sep
|
Bayshore HealthCare
|
Trois-Rivières

08 Sep

Bayshore HealthCare

Trois-Rivières

This is a casual position based in the Trois‑Rivières region.

The Specialty Pharma

Nurse, Clinical Trials Registered Nurse (CTRN) reports directly to the Specialty Pharma Nurse Supervisor (SPNS) and/or Specialty Pharma Nurse Manager (SPNM). In this role, the CTRN works in close collaboration with the Scientific Affairs (SCA) team to deliver and monitor specialized infusion, injectable or oral pharmacological treatments, investigational medicinal products in the home and/or clinic setting. The CTRN administers protocol‑specific nursing care to participants in home, clinic or community settings within decentralized or hybrid trials.

This position upholds patient care standards, ensures strict protocol and regulatory compliance, and serves as the primary liaison for the sponsor and study team in the participant’s environment. The CTRN is responsible for monitoring the patient for clinical trial study‑related reactions, accurately documenting procedures on electronic charts or source documents, and submitting reports in a timely manner. The CTRN is expected to maintain effective communication with the SPNS and/or SPNM along with the Scientific Affairs Team to ensure patient safety and satisfaction.

Specialized pharmacological or clinical trial training will be provided. This role offers the chance to specialize in clinical trial support and actively contribute to clinical research initiatives. Bayshore has a focus on nursing education and provides many opportunities for nurses to advance their professional growth.

A minimum commitment of two days per week, Monday through Friday, is required. The CTRN ensures a one‑on‑one patient experience, and we strive to ensure that patients stay with the same nurse to ensure the best quality and continuity of care. Ce poste exige que l’infirmier(ère) suive toutes les formations obligatoires prévues par les protocoles et règlements des essais cliniques, y compris une formation théorique approfondie.

Veiller au respect des bonnes pratiques cliniques (BPC),



des directives du Conseil international d’harmonisation (CIH), des procédures opérationnelles normalisées (PON) et des exigences réglementaires locales. Élaborer et réviser des plans de soins infirmiers personnalisés pour chaque patient(e). Effectuer des évaluations de l’état de santé des patient(e)s et enseigner les procédures d’administration des médicaments.

Effectuer le traitement, l’emballage, la centrifugation et l’expédition des échantillons de laboratoire conformément au protocole, aux exigences relatives aux marchandises dangereuses et aux exigences du promoteur. Préparer et administrer divers médicaments spécialisés ou expérimentaux intraveineux ou des traitements pharmacologiques injectables à des patient(e)s de tous âges, conformément au protocole. Fournir les soins aux patient(e)s en utilisant les compétences d’observation, d’évaluation, de diagnostic infirmier, de conseil et d’enseignement sanitaire, et signaler tout événement indésirable au superviseur immédiat ou aux parties prenantes requises.

Effectuer les tâches infirmières courantes conformément aux politiques et aux procédures de l’entreprise ainsi qu’aux normes de l’organisme provincial de réglementation des soins infirmiers. Veiller à ce que la documentation soit précise, opportune et conforme aux protocoles afin d’assurer l’intégrité des données et le respect des obligations contractuelles. Fournir des soins centrés sur le patient conformément au plan de soins établi ou aux directives médicales.





Effectuer des interventions de soins infirmiers spécialisés impliquant une formation reconnue et des compétences actuelles qui ont été démontrées et actualisées conformément aux normes. Maintenir les formations et les mises à jour liées au poste, selon les besoins. Observer et documenter l’état de santé des patient(e)s.

This role requires the nurse to complete all training mandated by clinical trial protocols and regulations, including extensive theoretical instructions. Ensure compliance with Good Clinical Practice (GCP), International Counsel of Harmonization (ICH) guidelines, Standard Operation Procedure (SOPs), and local regulatory requirements. Develop and review nursing care plans that are individualized to each patient.

Conduct patient health assessments and medication administration teaching. Demonstrated competency in phlebotomy including venipuncture across diverse patient populations. Perform lab sample processing, packaging, centrifuge operation and shipment in accordance with protocol, dangerous goods and sponsor requirements.

Coordinate and manage courier services for biological sample collection, study medication deliveries, and study supplies in accordance with protocols and temperature requirements. Provide patient care by utilizing the skills of observation, assessment, nursing diagnosis, counseling, health teaching, and reporting any adverse events to immediate supervisor or required stakeholders. Perform routine nursing duties in accordance with company policies and procedures, and provincial body standards.

Ensure accurate, timely and protocol‑compliant documentation to support data integrity and contractual obligations. Provide patient centered care according to the established care plan or medical directive. Perform specialized nursing procedures for which recognized training and current competencies have been demonstrated and updated per standards.

Maintain role related training and updates as required.

📌 Infirmier(ère) autorisé(e) en essais cliniques - Registered Nurse - Clinical Trials
🏢 Bayshore HealthCare
📍 Trois-Rivières

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