深圳招聘

SUMMARY OF PURPOSE/MAJOR RESPONSIBILITIES

Ensure good execution of PV reporting internally to GPV and externally CDCs in line with company compliance and local regulations; organize medical assessment and coordinate the management of compensation claim.


KEY ACCOUNTABILITIES

? Review and update PV SOP in line with national regulations and company internal procedures on a timely basis and ensure proper implementation once the SOP is approved by management.
- Execute PV reporting with quality in line with company SOP and local regulations Receive, record and check the PV report from all sources;
- Ensure expedited and periodic reporting of safety reports to GPV or SFDA/CDC in time;
- Follow up PV cases to obtain a full-scale medical information;
- Improve and administer the work to normalize archives and e-manage PV cases for powerful information search.
? Summarize and analyze PV cases periodically to bring forward advices to upper management, and transmit safety information issued by the GPV for internal or external use; collect and analyze the frequently asked questions in PV daily work to support company training and market activity.
? Provide additional safety data for business upon special requests of health authorities or other departments.
? Watch latest national and international PV policies, PV message of competitors and update to the management team.


REQUIREMENTS

? A degree in medical sciences from a credible university in China, with medical practical experience
? Preferable 1 years working experience in a similar position in foreign pharmaceutical enterprises. Experience in dealing with officials and healthcare professionals.
? Good command of English, both in verbal and in written. Competency equal to College English Test Band 6 or above.
? Good computer skills on Office Word, Excel, Power-point and Outlook, and office facilities.
? Advanced interpersonal and presentation skills
? Analytical, logical, well-organized mindset, and attentive to details.

深圳赛诺菲巴斯德生物制品有限公司诚聘