Clinical Study Manager
Philips
full-time
Posted on:
Location Type: Remote
Location: Remote • Pennsylvania • 🇺🇸 United States
Visit company websiteSalary
💰 $101,250 - $162,000 per year
Job Level
Mid-LevelSenior
Tech Stack
Google Cloud Platform
About the role
- oversees the execution and regulatory compliance of clinical studies
- manages documentation, negotiations, and team priorities
- conducts and oversees all aspects of clinical studies
- serves as a key resource and subject matter expert for study sites and investigators
- optimizes study efficiency and data quality through process improvements
- collaborates and builds effective relationships across internal teams
- monitors study progress against milestones, timelines, and budgets; proactively identifies risks
Requirements
- 5+ years of experience in execution of clinical research in the medical device industry (preferred), pharma, biotech, academia, or government research required
- 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.)
- Doctorate degree or higher in a related field
- strong attention to detail
- a learner mindset
- coachable
Benefits
- generous PTO
- 401k (up to 7% match)
- HSA (with company contribution)
- stock purchase plan
- education reimbursement
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical researchclinical trials designregulatory compliancedata qualityprocess improvementsrisk identificationdocumentation managementnegotiationstudy monitoringmilestone tracking
Soft skills
attention to detaillearner mindsetcoachablecollaborationrelationship buildingteam managementcommunicationproblem-solvingleadershiporganizational skills