Clinical Study Manager Neurovascular (m/f/d)

At Penumbra,innovation,teamwork, andinitiativeare more than values–they are the foundation of a workplace where every individual is encouraged to grow and make a real difference. We believe that the strength of our team lies in our diverse talents and shared passion for improving lives. Ifyou’relooking for a role where your contributions matter, we invite you to join a company that values both personal development and impactful work.

As a leading MedTech company,weprovidecutting-edgesolutions for conditions such as stroke, pulmonary embolism, deep vein thrombosis, and acute limb ischemia.Headquarteredin Alameda, California, Penumbra has over 4,500 employees worldwide and generated revenues of approximately $1.4 billion in 2025.

What is in it for you

• Stay Active - Enjoy an annual fitness subsidy to support your healthy lifestyle.
• Support & Well-Being - Benefit from our comprehensive Employee Assistance Program, providing guidance and support in times of need.
• Family First - Receive two weeks of paid Family Care Leave to support a sick family member or in the case of bereavement.
• Vacation Time - In addition to your regular vacation days, enjoy paid time off on December 24th and 31st.
• A Team That Inspires - Work alongside a diverse, open-minded, and supportive team that encourages personal and professional growth.
• Accident Insurance - Stay protected with comprehensive accident insurance during all business trips.

Main Responsibilities

• Lead and manage international clinical studies from study start-up through close-out, ensuring delivery on time, within budget, and in compliance with applicable regulations.
• Coordinate investigator sites across Europe and internationally, providing operational support throughout the study lifecycle.
• Manage study timelines, budgets, documentation, clinical systems, and trial dashboards.
• Oversee external vendors, Investigator Meetings, and collaborations with Principal Investigators (PIs) and Key Opinion Leaders (KOLs).
• Monitor study progress, identify risks, and drive timely issue resolution to ensure successful study execution.
• Support clinical data review, regulatory submissions, and study reporting.
• Partner with cross-functional teams including Regulatory Affairs, R&D, Medical Affairs, Quality, Marketing, and Commercial.
• Drive compliance with ICH-GCP, QMS, and applicable regulatory requirements while contributing to continuous process improvements.

What we are looking for

• Bachelor's degree in Life Sciences or a related scientific discipline.
• 3–5+ years of clinical study or clinical project management experience within MedTech, medical devices, or the pharmaceutical industry.
• Hands-on experience managing international, multicenter clinical studies, including site management, vendor oversight, and study execution.
• Strong knowledge of ICH-GCP, clinical study operations, and regulatory requirements.
• Experience working within a global, cross-functional matrix organization.
• Excellent project management, stakeholder management, and communication skills.
• Proficiency with EDC systems, clinical trial management tools, and Microsoft Office.
• Experience inNeurovascular , Cardiovascular , or another interventional medical device area is highly desirable.
• Willingness to travel up to20% across Europe and internationally.

At Penumbra, we value your skills and qualificationsabove all else. We welcome candidates of any gender, ethnicity, religion, sexual orientation, or age. Ifyou'reskilled and a good match for our culture of collaboration, we want you on our team.

To learn more about Penumbra's commitment to being an equal opportunity employer, please take a look atour AAP-Policy-Statement.