Lead Medical Director (ophthalmology)

Roche

Shanghai, China
**
M.d. degree with relevant medical experience
4+ years pharma/biotech industry experience
4+ years clinical trials experience phase ii-iii
** Roche is seeking a Lead Medical Director in Ophthalmology to oversee clinical development strategies and plans for assigned molecules, ensuring effective execution of clinical trials. The ideal candidate should possess significant medical experience, particularly in ophthalmology, and have demonstrated leadership in clinical development within the pharmaceutical industry. **

Job Summary

  • The Lead Medical Director is responsible for developing and executing late-stage clinical strategies to deliver medically-differentiated therapies.
  • This role requires leading cross-functional teams and representing the company in interactions with health authorities and key opinion leaders.
  • Roche offers a culture that encourages personal expression, open dialogue, and genuine connections where every voice matters.

Matching Summary

Match Score: 75

** Roche is seeking a Lead Medical Director in Ophthalmology to oversee clinical development strategies and plans for assigned molecules, ensuring effective execution of clinical trials. The ideal candidate should possess significant medical experience, particularly in ophthalmology, and have demonstrated leadership in clinical development within the pharmaceutical industry. **

Skills & Requirements

Must-have

  • M.D. degree with relevant medical experience
  • 4+ years pharma/biotech industry experience
  • 4+ years clinical trials experience Phase II-III
  • Cross-functional team leadership skills
  • Global clinical development planning expertise

Nice-to-have

  • Experience submitting NDA/BLA to regulatory authorities
  • Authoring global clinical development plans
  • Publishing results in peer-reviewed journals
  • Academic or teaching background
  • Previous people management experience

Key Requirements

  • M.D. required
  • 4+ years pharmaceutical industry experience
  • In-depth understanding of Phase II-III drug development
  • Experience with NDA/BLA submissions preferred
  • Proven track record in clinical study design and oversight

Work Rights

Not specified

Tailored Resume

Cover Letter