Clinical Research Associate jobs in Montréal, QC
Assistant aux essais cliniques / Clinical Trial Assistant
Easily applyUrgently hiringNeuroRx ResearchMontréal, QC- $26.84–$74.71 an hour
- Full-time +1
- Monday to Friday
- Vision care
- Extended health care
- Prepare and issue trial-specific reports and queries to clinical sites.
- The Clinical Trial Assistant (CTA) provides administrative support to Project Managers…
Coordonnateur du contrôle de la qualitéb / Quality Control Coordinator
Easily applyUrgently hiringNeuroRx ResearchMontréal, QC- $46,624.54–$85,733.87 a year
- Full-time
- Monday to Friday
- Extended health care
- Experience in Quality Control and/or clinical trials is an asset.
- QC of quantitative measurement results in database against source documents prior to scheduled…
- AccentureMontréal, QC
- $82,600–$132,600 a year
- Full-time
- Experience and certification in at least one certification in one of Epic's clinical apps (EpicCare Ambulatory, ClinDoc, Cupid, Orders, Radiant, etc).
- View all Accenture jobs - Montréal jobs - Clinical Associate jobs in Montréal, QC
- Salary Search: Epic Clinical Associate Manager or Manager salaries in Montréal, QC
- See popular questions & answers about Accenture
- IQVIAKirkland, QC
- $116,300–$193,800 a year
- May act as a lead clinical manager alongside other clinical managers for the execution of large-scale international clinical trials.
- IQVIAKirkland, QC
- $111,800–$149,000 a year
- Full-time
- 7+ years of clinical research experience, including 4+ years in project management.
- Strong knowledge of clinical trial conduct, regulatory requirements, and…
- IQVIAKirkland, QC
- $73,600–$170,900 a year
- Full-time
- Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference…
View similar jobs with this employerAltasciencesMontréal, QC- Full-time
- Day shift +2
- Effectuer les inspections programmées des chariots d'urgence, inventorier et inspecter leur contenu, et tenir à jour les registres.
- View all Altasciences jobs - Montréal jobs - Infirmier (H/F) jobs in Montréal, QC
- Salary Search: Clinical Research Nurse salaries in Montréal, QC
- See popular questions & answers about Altasciences
Safety Lead
Easily applyPrecision for MedicineMontréal, QC- 10+ years clinical safety experience.
- Excellent judgment and ability to communicate complex clinical issues in a scientifically sound and understandable way.
- View all Precision for Medicine jobs - Montréal jobs - Shift Leader jobs in Montréal, QC
- Salary Search: Safety Lead salaries in Montréal, QC
Safety Lead
Easily applyPrecision for MedicineMontréal, QC- 10+ years clinical safety experience.
- Excellent judgment and ability to communicate complex clinical issues in a scientifically sound and understandable way.
- View all Precision for Medicine jobs - Montréal jobs - Shift Leader jobs in Montréal, QC
- Salary Search: Safety Lead salaries in Montréal, QC
- IQVIAKirkland, QC
- Part-time
- Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral research).
- Minimum 3 years of clinical experience with psychiatric…
- View all IQVIA jobs - Kirkland jobs
- Salary Search: Clinical Independent Rater (CIR) – French Speaking salaries
- See popular questions & answers about IQVIA
- IQVIAKirkland, QC
- $124,400–$207,300 a year
- Full-time
- Knowledge of clinical trials - Knowledge of clinical trial conduct in addition to skill in applying applicable clinical research regulatory requirements i.e.
- View all IQVIA jobs - Kirkland jobs - Chef de Projet Informatique (H/F) jobs in Kirkland, QC
- Salary Search: responsable clinique / Clinical Lead salaries
- See popular questions & answers about IQVIA
- IQVIAKirkland, QC
- $103,000–$137,280 a year
- Full-time
- At least 5 years with 2 years of lead experience in a scientific or clinical environment.
- Execute operational strategy/ expectations for maintenance of clinical…
- AltasciencesLaval, QC
- The requirement to have study protocols, designs and clinical research documents written and documented in English as required by industry regulatory agencies.
- View all Altasciences jobs - Laval jobs - Associate Scientist jobs in Laval, QC
- Salary Search: Associate Scientist (BSD) salaries in Laval, QC
- See popular questions & answers about Altasciences
- AltasciencesMontréal, QC
- Full-time
- Ensure the confidentiality of clinical trial participants and sponsors is respected.
- Act as a liaison to the clinical/study operations teams.
- View all Altasciences jobs - Montréal jobs - Sample Manager jobs in Montréal, QC
- Salary Search: Sample Management Coordinator salaries in Montréal, QC
- See popular questions & answers about Altasciences
- AltasciencesMontréal, QC
- Part-time
- Day shift +3
- The requirement to have study protocols, designs and clinical research documents written and documented in English as required by industry regulatory agencies.
- View all Altasciences jobs - Montréal jobs
- Salary Search: Clinical Research Technician salaries in Montréal, QC
- See popular questions & answers about Altasciences
TMF Coordinator
Easily applyAlimentivMontréal, QC- $42,000–$70,000 a year
- Full-time +1
- Ensure proper management of essential clinical trial documentation.
- Strong understanding of clinical trial record management and quality standards.
- View all Alimentiv jobs - Montréal jobs - Coordinator jobs in Montréal, QC
- Salary Search: TMF Coordinator salaries in Montréal, QC
- See popular questions & answers about Alimentiv
By creating a job alert, you agree to our Terms . You can change your consent settings at any time by unsubscribing or as detailed in our terms.
People also searched:
Career Resources:
Job Post Details
Assistant aux essais cliniques / Clinical Trial Assistant - job post
Job details
Pay
- $26.84–$74.71 an hour
Job type
- Permanent
- Full-time
Shift and schedule
- Du Lundi au Vendredi
Location
Benefits
Pulled from the full job description
- Vision care
- Extended health care
Full job description
Assistant aux essais cliniques
L’entreprise
NeuroRx Research est un chef de file en analyse avancée d’images cérébrales et en gestion de projets pour l’industrie pharmaceutique et biotechnologique. Nous nous spécialisons dans les activités liées à l’IRM à toutes les phases (I-IV) des essais cliniques de neurologie. Pour en savoir plus, consultez le site www.neurorx.com.
Le rôle
L’assistant aux essais cliniques (CTA) fournit un soutien administratif aux gestionnaires de projet et travaille en étroite collaboration avec les sites cliniques et les installations d’IRM.
L’assistant aux essais cliniques est supervisé et relève du directeur associé de la gestion de projet.
Période de probation : 6 mois
Principales responsabilités
· Soumettre des demandes d’expédition de fournitures MRI et de création de compte sFTP spécifique aux essais
· Préparer et transmettre aux sites cliniques des rapports et des demandes de renseignements propres aux essais
· Faire un suivi auprès des sites pour obtenir de la documentation et analyser les présentations
· Réception, traitement, contrôle de la qualité et rapport des résultats de l’IRM conformément aux SOP NeuroRx
· Entrées/importations de données dans les applications Web de NeuroRx
· Planifier et organiser des sessions de formation entre les sites et NeuroRx
Qualifications et compétences
Éducation
Un baccalauréat, de préférence en sciences.
Langues
· Anglais - Excellent oral et écrit
· Français - Connaissances de travail
Attributs
· Méticuleux, organisé, efficace et professionnel
· Indépendant et capable de prospérer dans un environnement dynamique
· Solides compétences en communication et en relations interpersonnelles
Compétences techniques
· Maîtrise de Microsoft Word, Excel, des plateformes de messagerie électronique et de l’utilisation d’Internet
· Expérience avec Mac OS X et Linux (actif)
Emplacement et admissibilité
· Doit vivre dans la grande région de Montréal
· Poste à distance, avec présence obligatoire au bureau une fois par semaine
· Permis de travail canadien valide requis
· Les candidats retenus doivent subir une vérification de leurs antécédents
Processus de demande
Veuillez soumettre votre CV ainsi qu’une lettre de motivation décrivant :
· Pourquoi vous êtes un candidat solide
· Vos attentes salariales
**Seuls les candidats sélectionnés seront contactés.**
Type d'emploi: Temps plein
Avantages: Soins de santé étendus
Calendrier: Du lundi au vendredi
Lieu de travail: En personne
_____________
Clinical Trial Assistant
The Company
NeuroRx Research is a leader in advanced brain image analysis and project management for the pharmaceutical and biotech industry. We specialize in MRI-related activities across all phases (I–IV) of neurology clinical trials. Learn more at www.neurorx.com.
The Role
The Clinical Trial Assistant (CTA) provides administrative support to Project Managers and works closely with clinical sites and MRI facilities.
The CTA is supervised and reports to the Associate Director of Project Management.
Probation period: 6 months
Key Responsibilities
- Submit requests for shipment of MRI supplies and trial-specific sFTP account creation
- Prepare and issue trial-specific reports and queries to clinical sites
- Follow up with sites for documentation and scan submissions
- MRI data receipt, handling, QC, and result reporting according to NeuroRx SOPs
- Data entries/imports into NeuroRx’s web-based applications
- Schedule and organize training sessions between sites and NeuroRx
Qualifications & Skills
Education
Bachelor’s degree, preferably in sciences.
Languages:
· English - Excellent oral and written
· French - Working knowledge
Attributes
- Meticulous, organized, efficient, and professional
- Independent and able to thrive in a fast-paced environment
- Strong interpersonal and communication skills
Technical Skills
- Proficiency in Microsoft Word, Excel, email platforms, and internet use
- Experience with Mac OS X and Linux (asset)
Location & Eligibility
- Must live within the Greater Montreal Area
- Remote position, with mandatory in-office presence once per week
- Valid Canadian work permit required
- Successful applicants must undergo a background check
Application Process
Please submit your CV and a cover letter outlining:
- Why you are a strong candidate
- Your salary expectations
**Only selected candidates will be contacted.**
Job Types: Full-time, Permanent
Pay: $26.84-$74.71 per hour
Benefits:
- Extended health care
- Vision care
Work Location: In person