• Provide guidance, lead/co-lead projects, manage own time to meet objectives and plan resource requirements for projects across the division.
• Oversee and support study start up activities at the country level, including review of key documents and providing support to address regulatory and/or ethics committee questions. Forecast and manage the Clinical Trial Budget.
• Approve and oversee drug supply management and manage flow of drug supply to the sites.
• Share and escalate plan deviations to Clinical Project Manager and study team.
• Help to address Significant Quality Events or other quality issues at patient and/or site level.
• Lead the data integrity and data quality activities for assigned protocols.
• Provide regional and cross-regional insights on study-site performance and trends to / from the study team.

• Bachelor's Degree
• 5+ years’ experience
• Demonstrated project management / leadership experience
• Experience working in the research and development of pharmaceutical industry
• Experience conducting, managing or participating in regulatory inspection processes
• Knowledge of project management discipline and its application to vaccine development
• Country level cultural awareness and strong interpersonal skills
• Excellent communication skills, both written and verbal in English and Dutch

• Master's degree
• Experience in early drug development
• Knowledge of the project management discipline and its application to vaccine/drug development

Medical