Medical Director

From Top Pharmaceutical Company with Competitive Teams in Hot TA

Your new company
Top Pharmaceutical Company with Competitive Teams in Hot TA

Your new role
  • Designing and implementing phase I-II-III clinical trials of innovative drugs in the field of tumours and autoimmune diseases in China and abroad, based on cGCP, ICH-GCP and other relevant clinical research guidelines;
  • Providing medical monitoring and guidance during clinical trials, including data security audits, participation in safety committees; communicating with regulatory authorities such as NMPA on medical research matters, and writing medical research documents for registration;
  • Medical support during the product development phase, including: medical knowledge of product design, medical analysis of competing products, translation and incorporation of medical data published in the scientific literature, providing medical rationale interpretation for Research and Development (R&D), and medical information support;
  • Providing medical strategic advice for product portfolio, project development, and introduction or transfer of researching products (rights and interests);
  • Maintaining effective communication and cooperation with investigators, ethics committees, clinical research institutions, patient groups, and regulatory authorities at all levels in accordance with relevant policies and regulations.

What you'll need to succeed
  • PhD in Medicine or in Life Sciences-related majors preferred;
  • Relevant years of experience in clinical trials in the field of oncology or autoimmune disease treatment, with successful implementation records from protocol design to full completion of Phase I-II-III clinical trials;
  • Comprehensive and in-depth understanding of the whole process of clinical trials of new drugs, including: design, implementation, and statistical/data management of clinical trials; Chinese and international norms and quality criteria; and requirements for pharmacovigilance;
  • Understanding and mastering GCP and ICH guidelines, and being familiar with FDA and NMPA regulations.


What you'll get in return
  • Amazing working experience in top pharmaceutical company with amazing teams
  • Competitive salary across the market

What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. #1219014

Summary

Job Type
Permanent
Industry
Pharmaceuticals
Location
Beijing
Specialism
Life Sciences
Ref:
1219014

Talk to a consultant

Talk to Fred Feng, the specialist consultant managing this position, located in Beijing
501, Tower 1, China Central Plaza, 81 Jianguo Road, Chaoyang District

Telephone: 01086487955

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