Senior Study Start Up Associate

This is a fully remote position, open to applicants in Netherlands.

📋 Description

• Operate within a sponsor-dedicated framework backed by ICON’s global expertise.

• Assist the Study Start Up Team Lead in formulating and implementing the strategy for country and site distribution within the Netherlands.

• Obtain approvals from Health Authorities and through the CTIS application to initiate assigned clinical trials.

• Oversee site start-up and activation responsibilities with a focus on technical precision, quality, and ongoing improvement.

• Conduct feasibility evaluations and identify suitable sites.

• Negotiate site contracts and execute other essential study start-up tasks.

• Offer expertise to Study Start Up team leads and project teams.

• Prepare and manage submissions to regulatory, ethical, and other pertinent organizations.

• Assist in the development, completion, and review of Master and Country Specific Subject Information Sheets/Informed Consent Forms.

⛳️ Requirements

• A Bachelor's degree or local equivalent, and/or relevant experience from a Medical/science background and/or discipline.

• A minimum of 3 years of experience or familiarity with clinical study start-up requirements and processes.

• Experience in Clinical Trial Submissions specific to the Netherlands.

• Proficiency in the local language as well as English.

• Willingness to travel as needed (approximately 5%).

• Legal authorization to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension schemes.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career advancement pathways.