Clinical Research Associate II/Senior CRA - French Fluency

@ Premier Research International LLC

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Télétravail au Canada

TélétravailTemps plein4+ ans d’expérience

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Premier Research International LLC is hiring a Clinical Research Associate II or Senior CRA with French fluency to join its Clinical Monitoring, Site Management and SSU team. The role runs on-site and remote monitoring visits for Phase I-IV and device trials, requires 70-85% travel, and is open to candidates based in Quebec.

Responsabilités :

Perform on-site and remote monitoring visits for Phase I-IV and device trials
Ensure clinical data validity, completeness and patient safety per ICH-GCP
Serve as primary contact for investigative sites and manage query resolution
Identify and escalate site risks and retraining needs
Plan monitoring visits and complete timely trip reports

Résumé des exigences :

Undergraduate degree or international equivalent
Minimum 4+ years on-site clinical research monitoring experience
French fluency and based in Quebec
Ability to complete 8-10 monitoring visits per month with 70-85% travel
Valid driver's licence and passport as required
Experience in oncology, neurology, rare disease or dermatology studies preferred

Outils et compétences

Clinical research Research Monitor activities Clinical trials Google Cloud DOS Valid driver's licence

Source et dates

Site carrière / système de candidatures · workday

Date publiée par l’employeur: 2026-10-25
Première détection par notre source: 2026-10-13
Mise à jour du dossier source: 2026-11-05

Ces dates décrivent le dossier source, pas une vérification en direct du recrutement. Consultez l’offre originale.

Détails du poste

Niveau	Intermédiaire
Domaine	Professions paramédicales
Expérience	4 an(s) et plus
Heures par semaine	40 (estimé)
Déplacements	avion : modérés · route : fréquents
Milieu de travail	Chez les clients, Domicile, Bureau
Position	Assis et debout
Exigences physiques	physique faible · ordinateur élevé
Langues	French, English
Permis de conduire	exigé
Formation	Baccalauréat (exigé)

Résumé et détails rédigés par l’IA à partir de l’offre; l’offre de l’employeur fait foi.

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Premier Research International LLC

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Offres sur Jobsy	2

Description

Premier Research is looking for a Clinical Research Associate II/Senior CRA - French Fluency to join our Clinical Monitoring, Site Management and SSU team.

You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.

We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.
Your ideas influence the way we work, and your voice matters here.
As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.

Join us and build your future here.

What you'll be doing:

Perform monitoring activities (both on site and remote) including Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits, Site Management Contacts, Close Out Visits for Phase I-IV clinical trials, as well as device trials with opportunities to work in the following Therapeutic areas: oncology, pediatrics, rare disease.
Ensure the validity, correctness, and completeness of clinical data collected at sites with a focus on data integrity and patient safety as dictated by trial protocol, ICH-GCP/ISO 141155, and customer requirements.
Serve as the primary point of contact for investigative sites, manage query resolution, support Trial Master File activities, participate in Investigators’ Meetings, and complete other project tasks in accordance with study timelines and budget.
Identify and escalate potential risks and possible retraining opportunities for investigative sites.
Schedule and plan day-to-day activities to include study monitoring visits, timely completion of high quality trip reports, and active management of all deliverables.

What we are searching for:

Undergraduate degree required or its international equivalent, along with minimum of 4+ years previous on-site clinical research monitoring experience required.
Must have French fluency and be based in Quebec
Known for being customer-focused in approach to work and communications with the ability to professionally interact with sites, clients, vendors and other functional areas
Experience with monitoring oncology/neurology/rare disease/dermatology studies are preferred
Accountable, dependable and strong commitment
Ability to meet the requirement of 8-10 DOS (Days on site)/monitoring visits/month; 70-85% travel
Valid driver’s license, passport as required