Medical Director, Clinical Development

Zymeworks

Cambridge, United Kingdom
On-site
Clinical study planning and conduct
Medical monitoring of clinical trials
Safety monitoring and gcp adherence
Zymeworks is developing a diverse pipeline of novel, multifunctional biotherapeutics to improve the standard of care for difficult-to-treat diseases

Job Summary

  • Zymeworks is developing a diverse pipeline of novel, multifunctional biotherapeutics to improve the standard of care for difficult-to-treat diseases.
  • This role will provide scientific and clinical leadership on all aspects of clinical study planning, conduct, and read-out, including medical monitoring and safety oversight.
  • The company offers a comprehensive total rewards package including competitive salaries, generous benefits, and opportunities for professional growth.

Matching Summary

Zymeworks is developing a diverse pipeline of novel, multifunctional biotherapeutics to improve the standard of care for difficult-to-treat diseases.

Skills & Requirements

Must-have

  • clinical study planning and conduct
  • medical monitoring of clinical trials
  • safety monitoring and GCP adherence
  • strategic partnerships with KOLs
  • cross-functional scientific leadership

Nice-to-have

  • improving standard of care
  • developing novel biotherapeutics
  • collaborative team environment

Key Requirements

  • MD or equivalent
  • 3-5 years oncology drug development experience
  • Oncology fellowship training preferred
  • ABIM Oncology certification preferred
  • Early-stage development and regulatory experience preferable

Work Rights

Not specified

Tailored Resume

Cover Letter