Sr. Medical Editor (regulatory Documents + Qc) - Us Home Based

Syneos Health

United States
Base: $62,000.00 - $108,600.00; bonus/equity: elig...
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Fda and eu regulatory guideline familiarity
Ama manual of style proficiency
Clinical study protocol and csr qc experience
** Syneos Health is seeking a Sr. Medical Editor specializing in regulatory documents and quality control to work from home in the U.S. The ideal candidate will have extensive experience with FDA and EU guidelines and will be responsible for ensuring the accuracy and quality of critical medical writing deliverables. **

Job Summary

  • The role requires maintaining strong familiarity with FDA, EU, and other relevant guidelines to ensure documents meet regulatory requirements.
  • Candidates will perform quality control reviews of clinical study protocols, reports, and investigator brochures while verifying data accuracy.
  • Syneos Health offers a comprehensive benefits package including health coverage, 401k matching, and performance-based bonuses.

Matching Summary

Match Score: 75

** Syneos Health is seeking a Sr. Medical Editor specializing in regulatory documents and quality control to work from home in the U.S. The ideal candidate will have extensive experience with FDA and EU guidelines and will be responsible for ensuring the accuracy and quality of critical medical writing deliverables. **

Salary

Base: $62,000.00 - $108,600.00; Bonus/Equity: Eligibility for commissions/bonus based on performance; Benefits: Medical, Dental, Vision, 401k match, PTO

Skills & Requirements

Must-have

  • FDA and EU regulatory guideline familiarity
  • AMA Manual of Style proficiency
  • Clinical study protocol and CSR QC experience
  • Data verification against source tables
  • Medical writing project management skills

Nice-to-have

  • Mentoring and training medical editing staff
  • Process improvement tool development
  • Cross-departmental collaboration experience
  • Agile problem-solving mindset
  • Inclusive culture participation

Key Requirements

  • Experience in regulatory medical writing
  • Proficiency with AMA style guidelines
  • Background in clinical study documentation

Work Rights

Not specified

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