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

IQVIA; Quebec; Remote; CAD 70,000 - 90,000; Full time

Job summary

A clinical research organization is seeking a candidate for a remote position in site monitoring and management. The ideal individual will have a BS/BA/BSc in life sciences or healthcare and at least four years of experience in clinical trials. Responsibilities include ensuring compliance, conducting site evaluations, and training personnel. This role offers a competitive salary with comprehensive benefits in a supportive environment.

Benefits

Opportunity for career advancement

Supportive work environment

Comprehensive benefits package

Qualifications

• Minimum of four years of experience in site monitoring/management.
• Strong knowledge of clinical research processes and medical terminology.
• Ability to travel domestically and internationally approximately 65% to 85%.

Responsibilities

• Conduct site evaluations for investigator recruitment.
• Ensure compliance with clinical study requirements.
• Monitor study initiation and closure visits.
• Train personnel on electronic data capture systems.

Skills

Site monitoring

Clinical trial coordination

Communication skills

Knowledge of clinical research

Education

BS/BA/BSc in life sciences or healthcare

Job description

Overview

Employer Industry: Clinical Research Services

Why consider this job opportunity

• Opportunity for career advancement and growth within the organization
• Work remotely anywhere within Canada
• Supportive and collaborative work environment
• Chance to make a positive impact on clinical trial outcomes and patient health
• Competitive salary and comprehensive benefits package

What to Expect

• Participate in the investigator recruitment process and conduct site evaluations
• Collaborate with site staff and regulatory bodies to ensure compliance with clinical study requirements
• Conduct study initiation, monitoring, and closure visits in accordance with protocols
• Train site personnel on electronic data capture (EDC) systems and ensure proper data management
• Serve as the primary contact between the employer and clinical investigators, coordinating all correspondence

Qualifications

• BS/BA/BSc (or equivalent) in life sciences or healthcare fields and a minimum of four years of experience in site monitoring/management
• Experience in monitoring and/or coordinating clinical trials is mandatory
• Strong knowledge of clinical research processes and medical terminology
• Excellent written and verbal communication skills
• Ability to travel domestically and internationally approximately 65% to 85%

Preferred Qualifications

• Previous experience in a clinical research organization (CRO)
• Experience in project team leadership
• Working knowledge of budget management
• Ability to mentor and co-monitor other Clinical Research Associates (CRAs)

#ClinicalResearch #ClinicalTrials #CareerOpportunity #RemoteWork #HealthcareJobs

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