Medical Writer, Hospital Patient Monitoring

Careers Philips

Base: $78,000 to $139,000; bonus/equity: annual in...
Fully remote
Clinical and post-market documentation authoring
Meddev 2.7.1 rev. 4 guidelines
Eu mdr regulations compliance
Philips is seeking a Medical Writer for Hospital Patient Monitoring to author and maintain clinical and post-market documentation. The ideal candidate should have experience in clinical research, particularly in the medical device industry, and possess strong writing and communication skills

Job Summary

  • You will be responsible for helping with authoring and maintaining clinical and post-market documentation such as CEPs, CERs, PMCFPs, and PMCFRs and contribute to our authoring other technical documents that support Clinical, Regulatory, Risk Management, or Post-Market Surveillance efforts.
  • Your role: Enforces rigorous adherence to Good Documentation Practices, meticulously maintaining the quality and accuracy of document content and format to meet stringent regulatory standards and internal protocols, working under direct supervision.
  • We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week.

Matching Summary

Match Score: 85

Philips is seeking a Medical Writer for Hospital Patient Monitoring to author and maintain clinical and post-market documentation. The ideal candidate should have experience in clinical research, particularly in the medical device industry, and possess strong writing and communication skills.

Salary

Base: $78,000 to $139,000; Bonus/Equity: Annual incentive bonus, sales commission or long-term incentives may be offered; Benefits: Generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement

Skills & Requirements

Must-have

  • Clinical and post-market documentation authoring
  • MEDDEV 2.7.1 Rev. 4 guidelines
  • EU MDR regulations compliance
  • Systematic literature searches
  • Data extraction and related tools
  • Good Documentation Practices (GDP)
  • AMA writing styles

Nice-to-have

  • Knowledge of bedside patient monitoring
  • Collaborative environment
  • Self-starter
  • Ability to learn quickly
  • Leading discussions
  • Presenting to stakeholders

Key Requirements

  • 1+ years clinical research experience
  • Master’s degree required
  • PhD/MD/PharmD in scientific/medical discipline preferred
  • US work authorization required

Work Rights

US work authorization

Tailored Resume

Cover Letter