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Medical Writer (FSP)

SHANGHAI, China 求人ID R0000029157 Category Medical Writing
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About this Role

-Responsible for the preparation of clinical documents on project and/or trial level required for advancing clinical development programs. This includes writing, planning, developing of document strategies, resolving and integrating review comments, and overseeing of timelines. Contribute to scientific and regulatory discussions within the trial and/or project teams. Requires proactive and continuous cross-functional coordination to ensure timely and successful document finalisation.

-Ensure quality of clinical documents assigned to external providers by appropriate oversight and training. Contribute to appropriate budget planning and cost control.

-Develop in-depth knowledge in the assigned TA and in one or more of the main document types of the function portfolio. Share knowledge with other medical writers (e.g. by giving presentations in team or group meetings).

-Advance MW standards by contributing to process improvement initiatives and working groups with cross-functional impact.

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