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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 * 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 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
