Lead CRA

In this role, you will manage local Monitors, supervising clinical monitoring and site management activities to verify the protection of trial subjects’ rights, safety and well-being, data quality and study compliance on a country/regional level.

Only CVs in English will be considered. 

You will:

• Facilitate regional projects as Lead Monitor and supervise study activities, timelines and schedules 
• Train Monitors in annotated monitoring visit reports
• Review monitoring reports and support monitors in their activities
• Act as the main communication line between Monitor and Regional Lead 
• Facilitate site budgets and contract negotiations
• Be a point of contact for in-house support services and vendors
• Communicate with internal project teams regarding study progress and lead project team calls on the country level 
• Participate in quality control and compliance monitoring
• May need to monitor and manage sites (if applicable)
• May need to supervise monitors on site
• Oversee and maintain study-specific and corporate tracking systems at site and country level

• College/University degree in Life Sciences, Pharmacy or an equivalent combination of education, training & experience
• Participation in clinical projects as a Lead/Senior Monitor
• At least 4 years of experience as Senior CRA
• Independent on-site monitoring experience
• Full working proficiency in English and Spanish
• PC skills to be able to work with MS Word, Excel and PowerPoint
• Ability to plan, multitask and work in a dynamic team environment
• Communication, leadership, and problem-solving skills
• Ability to travel

Advance your career in clinical research, overseeing a variety of tasks and growing with the company. You will work closely with driven and dedicated cross-functional teams, get all support and ownership of your projects.