Clinical Research Associate ensuring sites conduct studies and reporting data accurately. Monitoring, site management, and collaboration with the study team.
About the role
- Clinical Research Associate conducting Phase I to IV clinical trials in Canada. Collaborating with clinical teams to ensure compliance and study execution.
Responsibilities
- Participate in the preparation and conduct of clinical trials
- Oversee clinical investigations and perform site visits
- Ensure adherence to clinical best practices
- Collaborate with clinical trial managers and site staff
Requirements
- Minimum 3 years of monitoring experience
- Strong knowledge of the clinical research process
- Excellent communication skills in French and English
- Bachelor's degree in life sciences or healthcare
- Ability to work independently and manage multiple priorities
Benefits
- Health insurance
- Wellness programs
- Professional development opportunities
- Bonuses and/or other forms of compensation
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