Descripción de la oferta
Experteer Overview In this role you support the management and monitoring of clinical trial sites to ensure protocol adherence, regulatory compliance, and GCP standards. You will work with cross-functional teams to optimize site operations and data quality, and contribute to training and mentoring within the site management function. You’ll build strong relationships with site personnel while tracking performance and driving timely issue resolution. This is an opportunity to impact patient access to new medicines through efficient, compliant site management.Compensaciones / Beneficios
- Coordinate monitoring activities at clinical trial sites ensuring protocol adherence and timely issue resolution
- Assist in preparing and reviewing Investigator Site File and Trial Master File documentation for GCP compliance
- Collaborate with cross-functional teams to support trial sites across the study lifecycle
- Track site performance metrics, analyze data, and produce reports to improve site management efficiency
- Participate in training initiatives and mentor junior staff in clinical trial managementResponsabilidades
- Bachelor's degree in Life Sciences, Healthcare Administration, or Clinical Research
- Experience in clinical research, site management, or monitoring with understanding of GCP and trial processes
- Strong organizational and project management skills with ability to manage multiple priorities
- Excellent analytical skills and attention to detail
- Strong communication and interpersonal skills for relationships with site personnel and cross-functional teams
- Excellent English and Dutch language proficiencyRequisitos principales
- Competitive base salary
- Health and wellbeing programmes
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes
- Learning and development opportunities
