Clinical Study Manager Neurovascular (m/f/d)

📋 Description

• Lead international clinical studies from start-up to close-out, on time, within budget.
• Coordinate investigator sites across Europe and globally, providing support.
• Manage study timelines, budgets, docs, systems, and dashboards.
• Oversee external vendors, investigator meetings, and PI/KOL collaborations.
• Monitor progress, identify risks, and drive timely issue resolution.
• Support data review, regulatory submissions, and study reporting.

🎯 Requirements

• Bachelor's degree in Life Sciences or related discipline.
• 3–5+ years in clinical study or project management in MedTech/pharma.
• Hands-on international multicenter clinical study mgmt: site & vendor oversight.
• Strong knowledge of ICH-GCP, clinical ops, and regulatory requirements.
• Proficiency with EDC systems, CTMS, and Microsoft Office.
• Willingness to travel up to 20% across Europe and internationally.

🎁 Benefits

• Stay Active – annual fitness subsidy.
• Support & Well-Being – Employee Assistance Program.
• Family First – two weeks of paid Family Care Leave.
• Vacation Time – paid time off on December 24th and 31st.
• A Team That Inspires – diverse team that supports growth.
• Accident Insurance – coverage during business trips.