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该职位来源于猎聘 Delivers high-quality medical/scientific/strategic input and medical/scientific interpretation on specific product data in fulfilment of the development business objectives for registration  May provide pivotal medical input to new drugs, including but not limited to recently acquired assets, and to support drug development.  Support in all medical, scientific, strategic and clinical matters both Project Teams and drug development programs from lead compound identification to product registration and launch  Provide medical, scientific and strategic expertise, contribute to and/or prepare CDP and clinical trial related documents, including but not limited to Investigator Brochure, communication with regulatory authorities, clinical trial synopses, clinical trial protocols, clinical summaries, Clinical Study Report, with the support of other R&D functions and in line with IDP, RFIs/RFPs 任职要求: Basic Requirements:

  • Master degree above, Medicine, Clinical is must.
  • Fluently English is must.
  • More than 5 years experiences in clinician or clinical R&D are must.

Personality

  • Positive attitude, drive to do your best, learning attitude
  • Trustworthy and reliable for strong sense of responsibility and carefulness.
  • Patience and meticulousness is prefer.