interpretation of safety information collected from pre-clinical through to post-marketing, including medical requests on all drug safety matters from Regulatory Authorities for product portfolio. Support the collation interpretation of safety information collected from pre-clinical through to post-marketing, including medical requests on all drug safety matters from Regulatory Authorities. Involvement in the development of Risk Management bid defence meetings. Previous experience with authoring/reviewing PV procedures is preferred. Experience
interpretation of safety information collected from pre-clinical through to post-marketing, including medical requests on all drug safety matters from Regulatory Authorities for product portfolio. Support the collation interpretation of safety information collected from pre-clinical through to post-marketing, including medical requests on all drug safety matters from Regulatory Authorities. Involvement in the development of Risk Management bid defence meetings. Previous experience with authoring/reviewing PV procedures is preferred. Experience