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(Sr.)MSL
20-25K/月广东省-广州/硕士及以上/3-5年
秦女士今天来过
再鼎医药(上海)有限公司

职位详情

岗位职责

任职要求:
• Education: Clinical medicine major with a master's degree or higher.
• Languages: Fluent in English Reading, Writing and Speaking
• Experience:
• Proven ability to build credible relationships with KOLs.
• Knowledge of healthcare systems, ICH guidelines, GCP, and ethical guidelines.
• Understanding of clinical medicine, disease management, and medical research.
• Ability to analyze scientific information within strategic and regulatory settings.
• Proficiency with IT tools and technical platforms.
• Strong integrity, customer focus, and interpersonal skills.
• Ability to work effectively in a dynamic environment.
岗位职责:
KOL Management & Medical Support:
• Map and profile KOLs/decision makers.
• Build professional relationships and gain advocacy from KOLs.
• Collect and report insights impacting Zai Lab's plans and trial designs.
• Provide accurate scientific information to healthcare professionals.
• Support product listing in medical guidelines and formularies.
• Train healthcare professionals on new therapies.
Clinical Development Support:
• Identify and place clinical investigators in Zai Lab trials.
• Support investigational sites with cross-functional teams.
• Facilitate Investigator-Initiated Trials (IIT) process.
• Guide investigators on legal and financial regulations.
Information Management/Insights:
• Support medical and scientific meetings by collecting insights.
• Share competitive information post-meeting.
Internal Support:
• Provide medical training to Zai Lab colleagues.
• Screen business opportunities.
• Collaborate on projects assigned by the MSL Manager.
• Work with Medical Advisors and cross-functional teams.

任职要求

公司信息

再鼎医药(上海)有限公司

  • 上海
  • 1000-9999人
  • 生物制药
  • 上市公司
  • 不需要融资
再鼎医药是一家立足中国、全球运营的创新型生物制药公司,致力于为中国及全球的患者提供癌症、自体免疫及感染性疾病领域的创新药物。 再鼎医药总部位于上海,自2014年成立以来,已与多个全球领先的生物制药公司建立了合作伙伴关系,打造起广泛的后期创新候选药物产品线。对于寻求进入中国市场以及寻找国际临床开发长期战略合作伙伴的全球生物制药公司来说,再鼎医药凭借一系列成功合作案例,成为了业界最值得信赖的合作伙伴人选之一。通过这些成功合作,再鼎医药打造起中国创新生物技术公司中最强大的晚期肿瘤产品管线,拥有多个全球同类首个和/或同类最佳药物。同时我们正在不断提高内部研发能力,以进一步补充我们的产品线,目标是未来每年可以有1-2个全球新药临床试验申请(IND)。
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