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Clinical Physician-FSP

BEIJING, China 求人ID R0000030092 Category Clinical Trials
応募

About this Role

Responsibility:

  • More detailed day-to day responsibilities will include:
  • Protocol development, protocol review,
  • support of the study set-up, review 30-40 documents on average including CRF, e-diary, lab manuals, data monitoring plan, …
  • during the study conduct: develop training materials for the Investigators and Ops teams,
  • review data
  • interact with the Authorities,
  • briefing documentations for the Authorities,
  • prepare clinical trials application materials,
  • may cover strategy level activities.

Requirement:

1. Refer to PhD background, clinical or public affairs background;

2. having experience with vaccines clinical development;

3.pro-active, diligent, able to work independently and take ownership of their work;

4. Good in English skill

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