Freelance Senior Medical Writer experienced in medical devices

6 hours, 36 minutes ago
Contract
Senior
Technical Writing and Documentation
Excelya

Excelya

Excelya is a global CRO offering full-service, FSP, and Resourcing solutions to Biotech, Pharma, and Medical Device companies, prioritizing people-first healthcare advancements.

Professional Services
251-1K
Founded 2014

Description

  • Prepare PMCF, CER, CEP, and PMS documents for medical device projects.
  • Review relevant project and regulatory documents for accuracy and completeness.
  • Provide consultation and gap analysis for transition from MDD to MDR.
  • Respond to queries from regulatory authorities.
  • Conduct literature searches and appraise literature search data.
  • Interpret, evaluate, and translate medical research findings into clear documentation.

Requirements

  • Degree in Life Sciences.
  • At least 4-5 years of experience in medical writing.
  • Experience preparing medical device-related documents, including CEP, CER, PMCF, and PSP.
  • Fluent English language skills.
  • French language knowledge is a plus.
  • Experience with FDA submissions for medical devices is a plus.
  • Regulatory consultation experience is a plus.
  • Ability to work part-time in a fully remote role.
  • Candidates must be based in an EU country or Armenia.

Benefits

  • Fully remote work.
  • Part-time freelance engagement.
  • Opportunity to work on high-impact medical affairs projects across multiple countries.
  • Chance to contribute to Excelya’s growth in the healthcare and CRO space.

Interested in this position?

Apply directly on the company website

Apply Now

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