Job Search and Career Advice Platform

Enable job alerts via email!

Lead Evidence & Regulatory Communications

Eagleston Financial Group

United Kingdom

Hybrid

GBP 50,000 - 70,000

Full time

30+ days ago

Generate a tailored resume in minutes

Land an interview and earn more. Learn more

Job summary

A leading technology company in the United Kingdom is seeking a Lead for Evidence Analysis, Evaluation, and Communications. In this role, you will lead initiatives in translating clinical evidence into strategic impact, managing the development of Clinical Evaluation Reports, and collaborating on regulatory submissions. Ideal candidates will possess strong scientific writing and project management skills, a degree in a biomedical discipline, and at least 5 years of experience in the medical device or pharmaceutical sectors. This position offers generous benefits and a hybrid working model.

Benefits

Generous annual bonus
Pension schemes
Flexible vacation and time off
Private health and dental plans
Discounts on gyms and fitness clubs

Qualifications

  • Minimum of 5 years experience in medical device or pharmaceutical sectors.
  • Proven ability to conduct literature reviews and analyze clinical data.
  • Expertise in regulatory documents aligned with EU MDR.

Responsibilities

  • Lead the development of Clinical Evaluation Reports (CERs).
  • Conduct systematic literature reviews for regulatory submissions.
  • Act as subject matter expert during audits and regulatory reviews.

Skills

Literature reviews
Clinical data analysis
Regulatory document authoring
Scientific writing
Project management

Education

Degree in biomedical sciences or clinical discipline
PhD (preferred)
Job description
A leading technology company in the United Kingdom is seeking a Lead for Evidence Analysis, Evaluation, and Communications. In this role, you will lead initiatives in translating clinical evidence into strategic impact, managing the development of Clinical Evaluation Reports, and collaborating on regulatory submissions. Ideal candidates will possess strong scientific writing and project management skills, a degree in a biomedical discipline, and at least 5 years of experience in the medical device or pharmaceutical sectors. This position offers generous benefits and a hybrid working model.
Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.