Associé de recherche clinique, Télécommande– francophone (Canada), IQVIA Clinical Research Asso[...]

IQVIA; Montreal; Remote; CAD 65,000 - 85,000; Full time

Job summary

A leading clinical research organization in Montreal is seeking a Clinical Research Associate to oversee clinical trials, ensuring compliance and data integrity. The ideal candidate has at least four years of site monitoring experience and a degree in a life science or healthcare field. Join a supportive team that values career growth and innovation in medical treatments.

Benefits

Opportunity for career advancement

Supportive work environment

Involvement in innovative medical treatments

Qualifications

• Minimum of four (4) years of experience in site monitoring or management.
• Previous experience in a clinical research organization (CRO) preferred.
• Ability to mentor and co-monitor other clinical research associates.

Responsibilities

• Participate in the investigator recruitment process and conduct on-site evaluations.
• Collaborate with site staff to coordinate activities in preparation for study launch.
• Conduct study initiation and closure activities, ensuring compliance with guidelines.

Skills

Site monitoring

Excellent communication

Travel ability

Team leadership

Education

BS/BA/BSc in life science or healthcare

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

Overview

Why consider this job opportunity:

• Opportunity for career advancement and growth within the organization
• Supportive and collaborative work environment
• Chance to work on innovative medical treatments that improve patient outcomes
• Involvement in various phases of clinical trials from initiation to closure
• Opportunity to mentor and develop junior staff members

Responsibilities

• Participate in the investigator recruitment process and conduct on-site evaluations
• Collaborate with site staff to coordinate activities in preparation for study launch
• Conduct study initiation and closure activities, ensuring compliance with guidelines
• Train site staff on the EDC system and monitor data quality and integrity
• Serve as the primary contact between the employer and investigators, ensuring timely communication

Qualifications

• BS/BA/BSc (or equivalent) in a life science or healthcare field
• Minimum of four (4) years of experience in site monitoring or management
• Previous experience in a clinical research organization (CRO) preferred
• Excellent written and verbal communication skills
• Ability to travel domestically and internationally approximately 65% to 85%

Preferred Qualifications

• Previous project team leadership experience
• Working knowledge of budget management
• Experience in oncology or medical device research
• Proficiency in Microsoft Word, Excel, and PowerPoint
• Ability to mentor and co-monitor other clinical research associates

#ClinicalResearch #Oncology #CareerGrowth #ClinicalTrials #LifeSciences

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