Medical Writer Ii

ICON Clinical Research, LP

Shanghai, China
Medical writing
Clinical trial documents
Regulatory submissions
As a Medical Writer II at ICON, you will play a pivotal role in the development and preparation of clinical trial documents, regulatory submissions, and scientific publications, contributing to the advancement of inNvative treatments and therapies

Job Summary

  • As a Medical Writer II at ICON, you will play a pivotal role in the development and preparation of clinical trial documents, regulatory submissions, and scientific publications, contributing to the advancement of inNvative treatments and therapies.
  • Collaborating with cross-functional teams to prepare, write, and edit clinical study reports (CSRs), clinical protocols, investigator brochures (IBs), patient narratives, and other regulatory documents in compliance with internal standards and regulatory guidelines.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.

Matching Summary

As a Medical Writer II at ICON, you will play a pivotal role in the development and preparation of clinical trial documents, regulatory submissions, and scientific publications, contributing to the advancement of inNvative treatments and therapies.

Skills & Requirements

Must-have

  • medical writing
  • clinical trial documents
  • regulatory submissions
  • scientific publications
  • data analysis and interpretation
  • medical terminology proficiency

Nice-to-have

  • foster an inclusive environment
  • drive innovation and excellence
  • nurtures talent
  • well-being and work life balance

Key Requirements

  • minimum of 3 years of experience
  • Bachelor's degree in Life Sciences, Pharmacy, Medicine, or related field
  • Familiarity with regulatory requirements
  • Proficiency in Microsoft Office Suite

Work Rights

Not specified

Tailored Resume

Cover Letter