Senior Clinical Development Scientist

Philips UK

Colorado Springs, CO, US
Base: $133,000 - $237,000; bonus/equity: annual in...
On-site (full-time presence required)
Clinical development portfolio
Study design and validation
Regulatory compliance and strategy
Philips UK is seeking a Senior Clinical Development Scientist to lead clinical development strategies for its IGT Devices product line. The ideal candidate will have over 10 years of experience in the medical device industry, with a strong background in clinical development, regulatory compliance, and cross-functional collaboration

Job Summary

  • Provide strategic input for all clinical aspects of the end-to-end coronary clinical development portfolio, from initial concept through post-market products.
  • Collaborate closely with both internal teams and external stakeholders to ensure clinical safety and performance objectives are met.
  • Lead or support scientific discussions with regulatory agencies and notified bodies to advance clinical and regulatory strategies.

Matching Summary

Match Score: 85

Philips UK is seeking a Senior Clinical Development Scientist to lead clinical development strategies for its IGT Devices product line. The ideal candidate will have over 10 years of experience in the medical device industry, with a strong background in clinical development, regulatory compliance, and cross-functional collaboration.

Salary

Base: $133,000 - $237,000; Bonus/Equity: Annual incentive bonus, sales commission, or long-term incentives may be offered; Benefits: Comprehensive Philips Total Rewards benefits program including PTO, 401k, HSA, stock purchase plan, education reimbursement

Skills & Requirements

Must-have

  • clinical development portfolio
  • study design and validation
  • regulatory compliance and strategy
  • scientific writing and dissemination
  • GCP and ICH guidelines

Nice-to-have

  • strong analytical thinking skills
  • collaborate effectively with teams
  • goal-oriented environment

Key Requirements

  • 10+ years of experience in medical device industry
  • Master's degree or higher in Biomedical Science, Engineering, or Health related field
  • Experience with GCP, ICH, FDA (21 CFR 812), and EU regulations (ISO 14155, 14971, EU MDR)
  • Experience writing clinical development plans and reports
  • US work authorization required

Work Rights

US work authorization required

Tailored Resume

Cover Letter