Clinical Project Leader at Salvia BioElectronics

Eindhoven, North Brabant, Netherlands -

Full Time

Start Date

Immediate

Expiry Date

16 Sep, 26

Salary

75000.0

Posted On

18 Jun, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Trial Management, Medical Device Regulations, ICH-GCP, ISO 14155, CRO Coordination, Stakeholder Management, Risk Mitigation, Budget Management, Study Planning, Regulatory Submissions, Neuromodulation, Clinical Monitoring

Industry

Medical Equipment Manufacturing

Description

Your mission Do you have a strong track record in clinical studies within the medical device industry and are you motivated to lead studies that make real impact for patients? Are you motivated by the idea of bringing breakthrough therapies to patients through high-quality clinical studies? As a Clinical Project Leader at Salvia BioElectronics, you will play a key role in the execution of our clinical trials. From planning to close-out, you ensure studies run smoothly, meet quality standards, and deliver meaningful results. Your work directly contributes to advancing our neuromodulation therapy and improving the lives of people with migraine. Your Responsibilities Lead the execution of one or more clinical studies, from planning through to close-out Create and manage study timelines, milestones, and budgets Coordinate CROs, investigators, and clinical sites Oversee study start-up, monitoring, enrollment, and close-out activities Ensure compliance with ICH-GCP, ISO 14155, and applicable regulations Identify risks and proactively drive mitigation actions Collaborate with cross-functional teams such as Clinical, Regulatory, Quality, and Development Contribute to study-related documentation for regulatory submissions (EU MDR, FDA, others) Support internal teams with training on study protocols and procedures Your profile Bachelor’s or Master’s degree in Life Sciences, Biomedical Sciences, or a related field Minuimum 5 years of experience in clinical research or clinical trial management Experience in medical devices (implantables or higher risk class devices preferred) Strong understanding of GCP and clinical trial execution Structured, hands-on, and proactive Strong communication and stakeholder management skills Fluent in Dutch and English German is a plus Able to travel occasionally (approximately 10%) Living in the Netherlands within approximately 30 minutes from Eindhoven Why us? At Salvia BioElectronics, you’re not just joining a company; you’re joining a mission. We are developing an ultra-thin implant that could transform the treatment of chronic migraine, a debilitating neurological disease that affects millions worldwide. Recognized with the FDA Breakthrough Device Designation, our work is at the forefront of neuromodulation innovation. You’ll be part of a driven, international team combining cutting-edge science with a strong sense of purpose: helping people reclaim their lives. Do you have questions? About us At Salvia BioElectronics, we are on a mission to empower people with migraine to reclaim their lives. We are pioneering a novel neuromodulation therapy for chronic migraine. MySalvia Therapy features ultra-thin implants, designed to target key nerves involved in migraine, and is activated by the press of a button on a wearable device. Built for everyday life, it is currently being evaluated in clinical studies. Our commitment is to work toward a future of drug-free relief without compromise, so people with migraine can live life, uninterrupted. Founded and headquartered at High Tech Campus Eindhoven, the heart of the Dutch Brainport region, Salvia brings together skilled device makers and entrepreneurs with extensive experience in medical devices and neuromodulation. Active in the United States, Europe, and Australia, Salvia is advancing clinical development with the support of leading investors. What sets us apart is our ambition and our purpose: we are building solutions that make a real difference in patients’ lives. At Salvia, you’ll find a team-driven culture, room to grow with the company, and the opportunity to contribute to meaningful technologies every day. We put people first, guided by a patient-first ethos and strengthened by a diverse team that is 40 percent female and 18 nationalities strong, working together to drive inclusive innovation.

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Responsibilities

Lead the execution of clinical studies for neuromodulation therapy from planning through close-out. Coordinate with CROs and cross-functional teams to ensure compliance with quality standards and regulatory requirements.