Clinical Research Associate managing site activities across multiple protocols for a single sponsor. Engaging in monitoring, training, and recruitment efforts for clinical studies.
Responsibilities
Manage site activities and monitoring across France
Collaborate with sites to develop, drive and track subject recruitment plans
Deliver protocol and study training to assigned sites
Create and maintain monitoring visit reports and action plans
Where appropriate, co-monitor, train and mentor junior team members
Requirements
Degree in Life Sciences or equivalent nursing experience
Minimum 2 years of independent on-site monitoring experience
Experience managing multiple protocols across various drug indications with strong time-management skills
In-depth knowledge of GCP
Flexible and able to travel nationwide
Hold a full, clean French driving license
Strong verbal, written and presentation skills; fluency in English and French required
Benefits
Competitive salary and benefits package
Flexible working hours with office-based or home-based options
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