上海招聘

Responsibilities of Position:

Provide medical expertise, review and preparation of clinical sections of Chinese-specific documents supporting regulatory submissions in order to ensure medically accurate and strategically positioned submission documents. These tasks will be performed independently and/or in collaboration with Chinese Study Medical Experts.

- Review and/or support writing clinical sections of regulatory submission documents to China regulatory authority e.g. Clinical Summaries (efficacy and safety sections), company position papers, briefing documents, responses to the authority

- Verify translation of clinical session of regulatory documents

- Perform literature searches and distil published data into concise, powerful documents and slide kits

Desired Qualifications:

- Medical degree or other medicine related discipline including but not limited to public health, pharmacology and medical information ect.

- Good command of English is a must

- A team player with strong communication skill

A global leading company focus on the drug research, clinical research and providing Clinincal operation solution for world famous pharamcy company. We have over 9000 people all of the World and entered into China in 2005. Will with a good development plan to broaden and improve China business scale.