Senior Clinical Research Associate

Become a Senior Clinical Research Associate at IQVIA in Montréal. This role focuses on site management and monitoring for clinical trials while requiring bilingual fluency in French and English.

IQVIA is seeking a Senior Clinical Research Associate to oversee site activities in various therapeutic areas. The position demands extensive knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines to ensure compliance. You will manage site monitoring visits, recruitment strategies, and maintain regular communication to address ongoing project issues.

Key Responsibilities:

• Conduct site selection, initiation, monitoring, and close-out visits

• Oversee subject recruitment plans in collaboration with sites

• Provide protocol training to assigned clinical sites

• Evaluate site practices for regulatory compliance

• Document site management and monitoring visit outcomes

Requirements:

• Bachelor’s degree in a scientific or healthcare field

• Minimum 3 years of on-site monitoring experience

• Knowledge of clinical research regulations

• Proficiency in Microsoft Office Suite

• Strong verbal and written English communication skills

Use your expertise in clinical trials to make a significant impact at IQVIA in Montréal.
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