Clinical Development Scientist

ph3Job Description: Clinical Development Scientist /h3ulliLocation: Best, Noord-Brabant, Netherlands /liliJob Type: Full time /li /ulpbJob Responsibilities /b /pulliOwns and drives end‑to‑end clinical evidence strategy, defining and linking clinical need, value, TPP, claims, endpoints, and evidence to regulatory acceptance and post‑market requirements with full lifecycle traceability (AD → PDLM → PMS). /liliLeads clinical development in cross‑functional AD and PDLM core teams and drives program governance and cross‑project integration enabling global alignment. /liliOwns clinical study design, protocol development, and execution—driving end‑to‑end delivery (kick‑off to results) with optimal data strategy, data integrity, audit readiness, and proactive risk and timeline management. /liliLeads site/KOL engagement and all site‑facing activities (protocol communication, contracts, training) in collaboration with Clinical Science/CPM to ensure compliant execution, protocol adherence, and consistent understanding of product and data requirements. /liliOwns end‑to‑end data strategy and oversees data management in collaboration with data/engineering teams, ensuring data quality, completeness, annotation integrity, adherence to protocol and traceability, while resolving complex data challenges. /liliCollaborates with data/engineering teams on data infrastructure (catalogues, systems) for structured access, traceability. /liliOperationalizes real‑world data by identifying, integrating, and governing (data relevance, reliability and scientific validity) diverse data sources, and leads CER and PMCF analytics to generate and continuously assess clinical evidence on safety, performance, and benefit–risk for patient safety and in accordance with regulations and guidance documents. /liliDefines claims validation strategies and leads continuous post‑market evidence surveillance (PMCF/PMS), translating insights into updated claims, regulatory submissions, and expansion of clinical value, indications, and market positioning. /liliAuthors and oversees core clinical and regulatory documents (study protocols, CDMA, data strategies, CSRs, CERs, PMCF), ensuring compliant, evidence‑based, and traceable outputs, including integration into IFU and regulatory submissions (e.g., 510k, Technical Documentation, NMPA etc). /liliDrives program risk management and knowledge sharing to optimize execution and evidence generation, and bridges regional and global teams. /liliCommunicates insights and aligns stakeholders, builds KOL partnerships, and supports informed decision‑making. /liliDrives scientific dissemination by translating clinical and real‑world evidence into publications, presentations, and competitive insights. /liliDrives structured project management via ADO/Azure, aligning cross‑functional tasks, tracking dependencies, and ensuring clear ownership, prioritization, and timely execution. /li /ulpbYou’re the right fit if you have: /b /pulliMedical degree (physician) / Doctor of Medicine, or Medical Technical degree, or a Life Science degree, or a Quantitative Science degree (e.g., Medicine, Technical Medicine, Biomedical Engineering, Biotechnology, Epidemiology, Health Informatics, Data Science). /liliResidency Advanced Training in Diagnostic Radiology/Ultrasound domain /liliExperience with ultrasound imaging. /liliExperience with developing AI-features in Radiology/Ultrasound. /liliExperience with developing AI‑based medical devices. /liliExperience in Clinical Development / Clinical Research. /liliExperience in clinical evidence communication, research and analysis. /liliExperience in Medical Writing (CER, CSR, PMCF) and/or Scientific Publications is nice to have /liliExperience in MedTech, Healthcare Research, Real-World data analytics, Epidemiology, or related fields. /liliExperienced in regulatory compliance, process improvement and project management /liliExperience with data tools (R, Python, Power BI, Tableau, Git) is nice to have /li /ulpbPreferred Skills: /b /pulliRegulatory Compliance /liliClinical Evaluation and PMCF methodologies /liliClinical Evidence Generation Strategy /liliMedical and Regulatory Writing (CER, CSR, reports) /liliData Analysis and Interpretation /liliQuantitative and Real‑World Evidence Methods /liliProject and Program Management /liliStrategic Planning and Business Acumen /liliKPI and Performance Management /liliDocument Review and Audit Readiness /liliContinuous Improvement /liliMedical Terminology /li /ulpbHow we work together /b /ppWe believe that we are better together than apart. For this role, this means working in-person at least 3 days per week. /ppbAbout Philips /b /ppWe are a health technology company. /p /p #J-18808-Ljbffr