Manager Clinical Programs, Neurovascular

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

📋 Description

• Lead and manage global and regional clinical programs, steering clinical strategy and ensuring successful execution of studies from initiation to close-out.

• Supervise, mentor, and develop a team of Study Managers while guaranteeing effective resource allocation across various clinical projects.

• Foster cross-functional collaboration with Regulatory Affairs, Medical Affairs, R&D, Biostatistics, Data Management, Safety, Marketing, and other essential stakeholders.

• Establish and nurture strong relationships with Key Opinion Leaders (KOLs), investigators, CROs, Core Labs, and additional external partners.

• Supervise study timelines, conduct clinical data reviews, oversee safety activities, manage regulatory submissions, and lead governance meetings (e.g., DSMB/CEC).

• Manage vendor selection, contract oversight, and the performance of external partners to ensure high-quality delivery of studies.

• Contribute to the development of clinical protocols, CRF creation, scientific publications, and the generation of clinical evidence.

• Promote operational excellence through ongoing process improvements while maintaining compliance with ICH-GCP, QMS, and relevant regulatory standards.

⛳️ Requirements

• Bachelor's or Master's degree in Life Sciences or a relevant scientific field.

• Over 7 years of experience in clinical research or Clinical Operations, with at least 5 years in MedTech, medical devices, biotechnology, or pharmaceuticals.

• Minimum of 3 years of leadership experience, demonstrating a track record of developing and managing high-performing teams.

• Significant experience in leading global or regional clinical programs, covering clinical strategy, study oversight, vendor management, and resource planning.

• Extensive knowledge of ICH-GCP, CFR requirements, clinical study operations, and regulatory compliance (FDA experience is a plus).

• Proven experience collaborating with KOLs, investigators, CROs, and cross-functional stakeholders within an international matrix organization.

• A background in Neurovascular is highly preferred; experience in Cardiovascular or other interventional medical device therapies is also desirable.

• Possess a strategic, collaborative, and hands-on leadership approach, thriving in a dynamic small- to mid-sized MedTech environment.

• Proficient in 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.

🏝️ Benefits

• 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.