Senior Clinical Development Scientist

Job Title Senior Clinical Development Scientist Job Description The Senior Clinical Development Scientist will develop, generate, and disseminate clinical and economic evidence for Philips Ultrasound products. The role provides strategic guidance across the entire product lifecycle, drives execution of clinical programs, and ensures high-quality evidence to support regulatory and market access requirements. Responsibilities Contribute strategic guidance for clinical and economic evidence across the end‑to‑end (E2E) development process from ideation through post‑market. Collaborate with internal and external stakeholders to develop and lead clinical initiatives, including non‑clinical and clinical strategies for new product development and lifecycle management. Drive execution of clinical programs and trials to meet regulatory requirements, ensuring quality and timeliness. Work with investigators, IRBs/ECs, regulatory agencies, societies, and associations to support claims, reimbursement, and health‑economic outcomes. Participate in clinical evaluation documentation, including guidance on Post‑Market Clinical Follow‑Up (PMCF) initiatives and clinical investigation documents. Interpret and disseminate evidence generated, including Clinical Study Reports (CSRs), Clinical Evaluation Reports (CERs), abstracts, and peer‑reviewed manuscripts. Lead and support scientific discussions with regulatory agencies or notified bodies, review clinical evidence for marketing authorisation and line extensions, and liaise during sponsor regulatory inspections. Qualifications Minimum of 7+ years of clinical experience in FDA‑regulated medical device environments, focusing on clinical research, development, and real‑world evidence (RWE). Strong scientific background with experience validating AI algorithm clinical performance. Expertise in innovative clinical trial/ study design, registries, quality‑improvement initiatives, creation of data networks, and biostatistics. In‑depth knowledge of GCP, FDA, and EU‑MDR regulations, and design control for medical devices. Excellent writing skills to produce clinical documents such as CSRs, CERs, PMCF and final reports. Ability to produce original scientific documentation: study reports, regulatory filings, investigator brochures, internal reports, and scientific publications. Strong collaboration skills and influence decision‑making across cross‑functional teams. Analytical mindset with ability to present statistical methods and results to diverse audiences, including non‑statisticians. Minimum Master’s degree in Life Sciences, Medical Field, or comparable discipline (MD or Ph.D. desired). Location & Travel Position based in Bothell, WA or Cambridge, MA. Candidates must reside in or within commuting distance to these locations. Travel up to 15% of time is required. Compensation Pay range: $148,000 to $237,000 (Bothell, WA and Cambridge, MA). Compensation may vary based on experience, location, and business needs. Annual incentive, sales commission, and long‑term incentives may also be offered. Benefits Employees are eligible for a comprehensive Total Rewards program, including generous PTO, 401(k) with up to 7% match, HSA (with company contribution), stock purchase plan, education reimbursement, and more. Equal Employment Opportunity Statement We are an Equal Employment and Opportunity Employer, including disability and veteran. We are committed to providing equal employment and advancement opportunities for all qualified employees and applicants without regard to race, color, religion, sex, pregnancy, genetic information, citizenship status, veteran status, marital or domestic partner status or any other characteristic protected by law. Reasonable accommodations are available for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veterans’ Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990. Applicants requiring accommodation may contact View phone number on click.appcast.io, option5. #J-18808-Ljbffr Philips International