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. 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 Qualifications 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 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.