Job summary
This role involves leading and coordinating clinical trial site management teams across Europe, specifically in neuroscience/CNS studies. The manager will provide strategic oversight, collaborate with regional teams, and ensure high-quality clinical trial execution within a global contract research organization. Strong leadership, communication, and clinical research experience are essential, as well as proficiency in clinical trial management systems. Travel within the region may be required.
Location and work setup
- Location
- Oslo
- Work setup
- Remote
Responsibilities
Lead and direct clinical site management teams throughout the study lifecycle; oversee regional Clinical Trial Managers, coordinating their efforts; act as the main contact for site management issues in meetings with sponsors, investigators, and for bid defenses; develop and implement global monitoring strategies for site initiation, enrollment, management, and closeout phases; ensure compliance with clinical monitoring plans, budgets, and study tools; train and manage Clinical Research Associates on study requirements; participate in recruitment strategy development; forecast site visit schedules and manage staffing accordingly; mentor Clinical Trial Managers and perform co-monitoring visits when needed; support study teams during regulatory inspections or audits.
Qualifications
A four-year degree in biological, physical, or health sciences with at least 4 years in a senior clinical research associate role, or a two-year nursing or life sciences degree with a minimum of 6 years senior clinical research associate experience. Additionally, at least 2 years’ relevant experience as a Clinical Trial Manager or Lead CRA overseeing a CTM team is required. Proven experience in neuroscience/CNS clinical studies is mandatory. Excellent English communication skills and ability to lead remote teams are necessary. Willingness to travel is expected.