面議（經常性薪資達4萬元或以上） 台南市善化區 5年工作經驗 2天前更新
1. Participate in the design, execution, and oversight of clinical trials (Phase I–IV) and
BE studies, ensuring compliance with GCP and regulatory requirements.
2. Support the development and implementation of medical strategies from early-
stage development to post-marketing, including medical writing, KOL
engagement, and participation in scientific events.
3. Provide expert medical insights to assess the scientific and clinical value of
pipeline products.
4. Collaborate with cross-functional teams (e.g., Regulatory, Marketing, Sales Teams)
to ensure consistency in medical messaging and support key business decisions.
5. Establish and maintain strong relationships with KOLs and clinical investigators,
acting as the primary medical liaison.
6. Preparing scientifically accurate and compliant medical content, including
presentations, product documents, and training materials.
7. Monitor and analyze relevant medical data, literature, clinical guidelines, and
competitive intelligence to provide internal strategic recommendations.
8. Assist in the preparation and writing of regulatory documents including INDs and
NDAs, ensuring scientific rigor and regulatory alignment.
展開 員工宿舍年節獎金年終獎金三節獎金激勵獎金
