Senior Study Start Up Associate

• Work in a sponsor-dedicated model supported by ICON’s global expertise
• Support the Study Start Up Team Lead in developing and executing the plan for country and site distribution in the Netherlands
• Acquire approval from Health Authorities and via the CTIS application to start up assigned clinical trials
• Lead site start-up and activation tasks with technical depth, focusing on quality and continuous improvement
• Conduct feasibility assessments and site identification
• Negotiate site contracts and perform other critical study start-up activities
• Provide expertise to Study Start Up team leads and project teams
• Prepare and coordinate submissions to regulatory, ethics, and other relevant bodies
• Contribute to developing, finalizing, and reviewing Master and Country Specific Subject Information Sheets/Informed Consent Forms

• A Bachelor's degree or local equivalent and/or appropriate experience from the Medical/science background and/or discipline
• At least 3 years of experience or understanding of clinical study start-up requirements and activities
• Experience in Clinical Trial Submissions for the Netherlands
• Fluency in the local language and English
• Willingness to travel as required (approximately 5%)
• Legal right to work in the country where the role is based

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways