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Clinical Study Manager
PhilipsClinical Study Manager overseeing the execution and regulatory compliance of clinical studies at Philips. Collaborating with cross-functional teams to optimize study efficiency and ensure compliance with regulatory standards.
Posted 6/17/2026full-timeRemote • Pennsylvania • 🇺🇸 United StatesMid-LevelSenior💰 $102,000 - $182,000 per yearWebsite
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
clinical researchclinical trials designregulatory compliancedata quality optimizationprocess improvementsrisk identificationissue resolutionstudy progress monitoringbudget managementmedical device standards
Soft Skills
attention to detaillearner mindsetcoachablecollaborationproblem-solvingcommunicationleadershiporganizational skillsproactive approachadaptability
Certifications & Qualifications
ISO 13485ISO 14155ICH/GCP guidelines
Industry Keywords
medical device industrypharmabiotechacademic researchgovernment researchclinical studiesregulatory standardsFDAGCPPhilips procedures
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Oversees the execution and regulatory compliance of clinical studies
- Conducts and oversees all aspects of clinical studies, ensuring strict compliance with regulatory standards (ISO, GCP, FDA) and Philips procedures
- Optimizes study efficiency and data quality through process improvements
- Collaborates with Clinical, Medical, Biostatistics, Data Management, Regulatory, Quality, R&D, and other internal teams
- Monitors study progress against milestones, timelines, and budgets; proactively identifies risks and resolves issues
Requirements
What you’ll need- 5+ years of experience in execution of clinical research in the medical device industry (preferred), pharma, biotech, academia, or government research
- knowledge of medical device clinical trials design and best practices (strongly preferred)
- familiarity with relevant medical device standards preferred (ISO 13485, 14155, ICH/GCP guidelines, etc.)
- bachelor's degree or higher, master's preferred
- strong attention to detail
- learner mindset
- coachable
- Up to 10% travel required based on business needs
- Must be based in the local Pittsburgh, PA area for proximity to study site locations.
Benefits
Comp & perks- PTO
- 401k (up to 7% match)
- HSA (with company contribution)
- stock purchase plan
- education reimbursement