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

IQVIA; Remote; CAD 163,000 - 193,000; Full time

Job summary

A leading clinical research organization in Montreal is seeking a Clinical Research Associate to monitor and manage clinical trials. Responsibilities include participating in investigator recruitment, ensuring regulatory compliance, and serving as the primary contact with investigators. The ideal candidate will hold a degree in life sciences or healthcare and have at least 4 years of experience in site monitoring. This role requires travel, with opportunities for career advancement and a competitive salary of up to $192,500 annually.

Benefits

Opportunities for career advancement

Collaborative work environment

Travel opportunities

Qualifications

• Minimum of four (4) years of experience in site monitoring/management.
• Experience in monitoring and/or coordinating clinical trials.
• Valid driver's license and ability to travel as required.

Responsibilities

• Participate in the investigator recruitment process.
• Collaborate with site staff to ensure regulatory compliance.
• Conduct study initiation and closure activities.
• Monitor clinical trials for adherence to good clinical practices.
• Serve as the primary contact between employer and investigators.

Skills

Site monitoring

Site management

Excellent written and verbal communication skills

Organizational skills

Interpersonal skills

Ability to manage multiple priorities

Team leadership

Education

BS/BA/BSc in life sciences or healthcare field

Job description

Employer Industry: Clinical Research Services

Why consider this job opportunity:

• Salary up to $192,500.00 annually
• Opportunity for career advancement and growth within the organization
• Collaborative and supportive work environment
• Chance to work on innovative medical treatments that improve patient outcomes
• Involvement in diverse clinical trials across various phases
• Travel opportunities both domestically and internationally (approximately 65% to 85%)

What to Expect (Job Responsibilities):

• Participate in the investigator recruitment process and conduct on-site evaluation visits of potential investigators
• Collaborate with site staff to coordinate activities in preparation for study launches and ensure regulatory compliance
• Conduct study initiation and closure activities, including training site staff on study procedures and EDC systems
• Monitor clinical trials to ensure adherence to good clinical practices and validate source documentation
• Serve as the primary contact between the employer and investigators, ensuring timely communication and data transmission

What is Required (Qualifications):

• BS/BA/BSc (or equivalent) in a life sciences or healthcare field and a minimum of four (4) years of experience in site monitoring/management
• Mandatory experience in monitoring and/or coordinating clinical trials
• Excellent written and verbal communication skills
• Strong organizational and interpersonal skills with the ability to manage multiple priorities
• Valid driver's license and ability to travel as required

How to Stand Out (Preferred Qualifications):

• Previous experience in a clinical research organization (CRO)
• Experience in leading project teams
• Working knowledge of budget management
• Familiarity with GCP/ICH guidelines and electronic data entry systems
• Ability to mentor and train other CRAs

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