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Clinical Project Lead

BOM·Tilburg (Noord-Brabant)VastMedior
Salaris niet vermeld
Vox-samenvatting
  • Rolomschrijving: Leidt klinische studies van planning tot afsluiting, bewaakt kwaliteit, tijdlijnen en budgetten, en coördineert met CRO's, onderzoekers en klinische locaties.
  • Vereiste ervaring: Minimaal 5 jaar ervaring in klinisch onderzoek of klinische trial management, met kennis van medische apparaten en GCP.
  • Vaardigheden en talen: Sterke communicatie- en stakeholdermanagementvaardigheden, vloeiend in Nederlands en Engels, Duits is een plus.
  • Werkomstandigheden: Werkt op locatie in Nederland, met mogelijkheid tot reizen (ongeveer 10%), en woont binnen 30 minuten van Eindhoven.
  • Opleiding: HBO of WO diploma in Life Sciences, Biomedische Wetenschappen of een gerelateerd vakgebied.
Solliciteer bij de bronJe verlaat VoxJobs naar nationalevacaturebank.nl — de sollicitatie wordt rechtstreeks bij het bedrijf afgehandeld. nationalevacaturebank.nl

Functiebeschrijving

Clinical Project Lead Salvia BioElectronics Administration Netherlands Posted on Jun 19, 2026 Apply now 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.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 proceduresBachelor'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 EindhovenAt 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. Apply now Powered by Getro.com

Transparantiepaneel

Originele bron
nationalevacaturebank.nl
Geplaatst
16 jul 2026 · echte datum
Laatst geverifieerd
35 minuten geleden
Kwaliteitsscore
35/100
Salaris vermeld0
Bedrijf geïdentificeerd0
applyUrl0
postedAt15
Volledige beschrijving20

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