職位描述
崗位職責:
1. 依據(jù)公司產品、國家醫(yī)藥行業(yè)政策及行業(yè)發(fā)展趨勢，負責制訂產品醫(yī)學規(guī)劃和策略；
2. 主導（或指導下級開展）上市后醫(yī)學研究項目的開發(fā)、實施與全程管理，包括（但不僅限于）專家溝通、方案討論修訂、指導監(jiān)督CRA或MSL及數(shù)據(jù)分析總結發(fā)表等工作，整理相關醫(yī)學數(shù)據(jù)，跟進醫(yī)學臨床研究進展
3. 負責產品生命周期管理，通過推進課題研究對不同發(fā)展階段產品循證證據(jù)進行挖掘，并進行推廣
4. 建設和維護KOL網(wǎng)絡，建立公司專家?guī)欤?BR>5. 跟蹤相關領域的醫(yī)學信息，獨立或指導下屬開展產品醫(yī)學知識庫更新和培訓；
6. 依據(jù)產品線醫(yī)學與市場規(guī)劃，配合市場部開展各級學術會議；產品醫(yī)學相關問題的答疑；獨立或指導下屬協(xié)助市場部完成推廣資料的制作與審核；
7. 定期收集整理臨床試驗過程中發(fā)生的嚴重不良事件或非預期不良事件，跟蹤收集國內外相關藥物的不良反應的信息，并與本條線同事進行溝通、討論與整理。
8. 關注和了解與公司業(yè)務相關的最新醫(yī)學學術發(fā)展動態(tài)，并負責與學術機構進行項目合作的策劃和實施。
9. 關注行業(yè)最新動態(tài)，掌握相關產品或相關類別產品的市場信息，包括市場潛力、競爭對手、消費者態(tài)度、反饋等，為產品決策提供依據(jù)；
1. Responsible for formulating product medical plans and strategies based on company products, national pharmaceutical industry policies and industry development trends;
2. Lead (or direct the subordinate to carry out) the development, implementation and full management of post-launch medical research projects, including (but not limited to) expert communication, program discussion revision, guidance and supervision of CRA or MSL and data analysis & summary publication, follow-up medical clinical research progress ；
3. Responsible for product life cycle management, and provide evidence for products at different stages of development by promoting research ；
4. Build and maintain a KOL network and establish a company expert database;
5. Track medical information in relevant fields, and independently or instruct subordinates to carry out product medical knowledge base update and training;
任職資格:
1.臨床醫(yī)學等相關專業(yè)研究生及以上學歷；
2.八年以上醫(yī)學事務管理經驗，熟悉腫瘤領域；
3.具有優(yōu)秀的團隊領導能力及內外部溝通、協(xié)調能力
4.熟悉國家有關臨床試驗的法律法規(guī)，具有獨立的醫(yī)學研究能力。
5.具備敏銳的市場洞察力；具有很強的判斷與決策能力。
1. Graduate degree or above in clinical medicine or other related majors;
2. More than 10 years of experience in medical affairs management, familiar with the fields of tumor/cardiovascular/neural;
3. Excellent team leadership and internal and external communication and coordination skills
4. Familiar with national laws and regulations on clinical trials, with independent medical research capabilities.
5. Keen market insight; strong judgment and decision-making ability.
