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Manager Clinical Programs Neurovascular (m/f/d)

Penumbra -
Home Office

Jetzt bewerben

Details zur Stelle

vor 3 Stunden

Leistungen

Employee Assistance Program

Qualifikationen

Forschungserfahrung
Microsoft Office
Master
Bachelor
Führungserfahrung

Vollständige Stellenbeschreibung

At Penumbra, innovation, teamwork, and initiative are 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. If you’re looking 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, we provide cutting-edge solutions for conditions such as stroke, pulmonary embolism, deep vein thrombosis, and acute limb ischemia. Headquartered in 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 oversee global and regional clinical programs, driving clinical strategy and successful study execution from start-up through study close-out.
Manage, coach, and develop a team of Study Managers while ensuring effective resource planning across multiple clinical projects.
Drive cross-functional collaboration with Regulatory Affairs, Medical Affairs, R&D, Biostatistics, Data Management, Safety, Marketing, and other key stakeholders.
Build and maintain strong relationships with Key Opinion Leaders (KOLs), investigators, CROs, Core Labs, and other external partners.
Oversee study timelines, clinical data reviews, safety activities, regulatory submissions, and governance meetings (e.g., DSMB/CEC).
Lead vendor selection, contract oversight, and external partner performance to ensure high-quality study delivery.
Contribute to clinical protocols, CRF development, scientific publications, and clinical evidence generation.
Drive operational excellence through continuous process improvements while ensuring compliance with ICH-GCP, QMS, and applicable regulatory requirements.

What we are looking for

Bachelor's or Master's degree in Life Sciences or a related scientific discipline.
7+ years of clinical research or Clinical Operations experience, including 5+ years within MedTech, medical devices, biotechnology, or pharmaceuticals.
At least 3 years of people leadership experience, with a proven track record of developing and leading high-performing teams.
Strong experience leading global or regional clinical programs, including clinical strategy, study oversight, vendor management, and resource planning.
Deep knowledge of ICH-GCP, CFR requirements, clinical study operations, and regulatory compliance (FDA experience is an advantage).
Experience working closely with KOLs, investigators, CROs, and cross-functional stakeholders in an international matrix organization.
Background in Neurovascular is strongly preferred; experience in Cardiovascular or other interventional medical device therapies is highly desirable.
Strategic, collaborative, and hands-on leadership style with the ability to thrive in a dynamic small- to mid-sized MedTech environment.
Proficiency with CTMS, EDC systems, Microsoft Office, Microsoft Project, and other clinical project management tools.
Willingness to travel up to 20% for investigator meetings, congresses, site visits, and internal project meetings.

As we require fluently English skills and the process will involve English speaking colleagues, we are looking forward to receiving your CV in English.

At Penumbra, we value your skills and qualifications above all else. We welcome candidates of any gender, ethnicity, religion, sexual orientation, or age. If you're skilled 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 at our AAP-Policy-Statement.

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Erweiterte Suche

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