Manager Clinical Programs Neurovascular (m/f/d)

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.

Requirements

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.; Fluently English skills.

Nice to have

FDA experience; Background in Neurovascular; experience in Cardiovascular or other interventional medical device therapies

Benefits

Annual fitness subsidy; Comprehensive Employee Assistance Program; Two weeks of paid Family Care Leave; Paid time off on December 24th and 31st; Comprehensive accident insurance during all business trips; Work alongside a diverse, open-minded, and supportive team