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CER Writer

50371
  • Remote, UK
  • Permanent

CER Writer - Remote - Medical

 

About the Company:

We are looking for several experienced CER Writers to join a group of expanding medical device companies. You will join a close-knit team of specialists clinical and compliance staff.

 

Responsibilities:

  • Writing and contributing to Clinical Evaluation Reports and Plans, Post Market Clinical Follow-up Plans and Reports, and Summaries of Safety and Clinical Performance.
  • Conducting literature reviews.
  • Report and protocol generation.
  • Writing PMS Plans and Reports.
  • Updating instructions for use and risk assessments following clinical review.
  • Undertaking biological evaluations.
  • Sourcing BER data.

 

 

Requirements:

  • Educated to degree level in a relevant scientific or engineering discipline.
  • Experience writing clinical evaluation reports and plans for medical devices to EU MDR 745/2017.
  • Experience in conducting literature searches.
  • Excellent communication skills.
  • Ability to self-motivate and work autonomously.
Claire Collinson Client Director Regulatory, Quality & R&D Recruitment

Apply for this role

  • info@kinetica.co.uk
  • +44 (0)113 261 71 81
  • Kinetica (UK) Ltd, Floor 13, Whitehall Waterfront, 2 Riverside Way, Leeds, LS1 4EH, UK