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Expect questions on GCP/protocol adherence, bilingual patient communication, adverse-event reporting, and coordinating visits in a memory-clinic setting. Be ready with examples of consent, scheduling, and chart accuracy under tight windows.
Strong fit if you are an RN comfortable in French and English, detail-oriented with clinical documentation, and motivated by research in cognition/memory care rather than pure bedside staffing. On-site Montreal work (not remote).
As a Bilingual Study Coordinator (Nurse/RN) at Thememoryclinic in Montreal, you would typically screen and consent participants, run study visits, document vitals and assessments, track adverse events, and keep source and eCRF data audit-ready. French–English communication with participants, families, and the investigator is central; the day mixes clinic workflow with protocol checklists and sponsor queries.
No. The listing is for Montreal, QC with remote set to off—expect on-site clinic and study-visit work.
Bilingual French–English skill is core to the title; Quebec’s Francophone majority makes both languages practical with participants and teams.
Licensed nursing practice plus comfort with protocols, consent, and precise documentation; memory-clinic or research experience helps but is not stated in the listing data.
Thememoryclinic invites qualified candidates in Montreal, QC to apply for the Contrat de 18 Mois Coordonnatrice d'études bilingue (Infirmière) / 18 Month Contract Bilingual Study Coordinator (Nurse/RN) full-time opportunity. This 18-month contract position calls for a registered nurse who thrives in bilingual settings and can guide study activities with precision and care. What This Role Involves As the Contrat de 18 Mois Coordonnatrice d'études bilingue (Infirmière) / 18 Month Contract Bilingual Study Coordinator (Nurse/RN) at Thememoryclinic in Montreal, QC, you will serve as the central point for organizing study workflows, interacting with participants in both English and French, and applying nursing judgment to keep every process compliant and participant-focused. The work centres on translating protocols into reliable daily operations while fostering clear communication across all parties involved near Montreal. Your Responsibilities Oversee participant identification, eligibility checks, and enrolment steps for assigned studies Obtain, explain, and document informed consent in a bilingual format that respects participant needs Execute study-related nursing assessments, procedures, and safety monitoring according to protocol Collect, enter, and verify study data with accuracy and attention to source verification Coordinate visit scheduling, follow-up contacts, and necessary contacts with investigators or site teams Maintain regulatory documents and ensure study conduct aligns with ethical and procedural standards Provide seamless bilingual communication to French- and English-speaking participants and collaborators Identify and report adverse events or protocol deviations promptly while supporting corrective actions Qualifications Current registration as a Nurse / Infirmière (RN) in good standing, valid for practice in Quebec Proven ability to work fluently in both English and French, spoken and written Hands-on experience coordinating studies or performing research nursing duties preferred Solid grasp of study protocols, informed-consent processes, and documentation practices Excellent organisational, interpersonal, and problem-solving skills suited to a busy study environment Demonstrated reliability in managing multiple concurrent tasks while protecting participant welfare Willingness to commit fully to the 18-month full-time contract based in Montreal, QC About the Company Thememoryclinic is hiring for this role and offers a supportive team environment. Ready to Apply? To apply, complete your application directly on this page, or you'll be redirected to the employer's…
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