Associé(e), Recherche clinique / Clinical Research Associate (Montréal, Québec)

Employer Industry: Clinical Research and Pharmacovigilance

Why consider this job opportunity:

1. Competitive salary with potential for bonuses
2. Opportunity for career advancement and growth within the organization
3. Flexible work arrangements, including remote work options
4. Engaging and inclusive workplace culture that values diversity
5. Chance to make a meaningful impact on global healthcare through clinical research
6. Comprehensive benefits package that supports employee well-being

What to Expect (Job Responsibilities):

1. Develop strong relationships with clinical study sites and ensure continuity through all phases of the trial
2. Perform site management and monitoring activities in compliance with regulatory standards and protocols
3. Conduct remote and on-site monitoring visits, ensuring data integrity and subject safety
4. Communicate with investigators and site staff regarding protocol adherence and site performance issues
5. Collaborate with various departments and external stakeholders to support assigned sites

What is Required (Qualifications):

1. Minimum of two years of direct site management (monitoring) experience in the bio/pharma or Contract Research Organization sector
2. Bachelor's degree with a strong emphasis in science and/or biology
3. Fluent in French and English, with excellent communication skills
4. Solid understanding of clinical research regulations and Good Clinical Practice guidelines
5. Proven skills in site management and patient recruitment

How to Stand Out (Preferred Qualifications):

1. Experience with various clinical IT applications and an ability to adapt to new technologies
2. Strong analytical skills with the ability to manage complex issues effectively
3. Demonstrated ability to work independently across multiple protocols and therapeutic areas
4. Knowledge of Good Documentation Practices
5. Experience in conducting audits or inspections

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