Job Description
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.
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)
Oversee and maintain study-specific and corporate tracking systems at site and country level
Qualifications
College / University degree in Life Sciences, Pharmacy, RN or an equivalent combination of education, training & experience
Participation in clinical projects as a Lead / Senior Monitor
Independent on-site monitoring experience
Full working proficiency in English
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
Additional Information
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.
Excellent and flexible working conditions
Extensive training and friendly, collegial team
Competitive salary and benefits package
Opportunities for personal and professional growth 
