職位描述
崗位職責(zé):
1. 依據(jù)公司產(chǎn)品、國家醫(yī)藥行業(yè)政策及行業(yè)發(fā)展趨勢(shì)，負(fù)責(zé)制訂產(chǎn)品醫(yī)學(xué)規(guī)劃和策略；
2. 主導(dǎo)（或指導(dǎo)下級(jí)開展）上市后醫(yī)學(xué)研究項(xiàng)目的開發(fā)、實(shí)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(dǎo)監(jiān)督CRA或MSL及數(shù)據(jù)分析總結(jié)發(fā)表等工作，整理相關(guān)醫(yī)學(xué)數(shù)據(jù)，跟進(jìn)醫(yī)學(xué)臨床研究進(jìn)展
3. 負(fù)責(zé)產(chǎn)品生命周期管理，通過推進(jìn)課題研究對(duì)不同發(fā)展階段產(chǎn)品循證證據(jù)進(jìn)行挖掘，并進(jìn)行推廣
4. 建設(shè)和維護(hù)KOL網(wǎng)絡(luò)，建立公司專家?guī)欤?BR>5. 跟蹤相關(guān)領(lǐng)域的醫(yī)學(xué)信息，獨(dú)立或指導(dǎo)下屬開展產(chǎn)品醫(yī)學(xué)知識(shí)庫更新和培訓(xùn)；
6. 依據(jù)產(chǎn)品線醫(yī)學(xué)與市場(chǎng)規(guī)劃，配合市場(chǎng)部開展各級(jí)學(xué)術(shù)會(huì)議；產(chǎn)品醫(yī)學(xué)相關(guān)問題的答疑；獨(dú)立或指導(dǎo)下屬協(xié)助市場(chǎng)部完成推廣資料的制作與審核；
7. 定期收集整理臨床試驗(yàn)過程中發(fā)生的嚴(yán)重不良事件或非預(yù)期不良事件，跟蹤收集國內(nèi)外相關(guān)藥物的不良反應(yīng)的信息，并與本條線同事進(jìn)行溝通、討論與整理。
8. 關(guān)注和了解與公司業(yè)務(wù)相關(guān)的最新醫(yī)學(xué)學(xué)術(shù)發(fā)展動(dòng)態(tài)，并負(fù)責(zé)與學(xué)術(shù)機(jī)構(gòu)進(jìn)行項(xiàng)目合作的策劃和實(shí)施。
9. 關(guān)注行業(yè)最新動(dòng)態(tài)，掌握相關(guān)產(chǎn)品或相關(guān)類別產(chǎn)品的市場(chǎng)信息，包括市場(chǎng)潛力、競(jìng)爭(zhēng)對(duì)手、消費(fèi)者態(tài)度、反饋等，為產(chǎn)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(xué)等相關(guān)專業(yè)研究生及以上學(xué)歷；
2.八年以上醫(yī)學(xué)事務(wù)管理經(jīng)驗(yàn)，熟悉腫瘤領(lǐng)域；
3.具有優(yōu)秀的團(tuán)隊(duì)領(lǐng)導(dǎo)能力及內(nèi)外部溝通、協(xié)調(diào)能力
4.熟悉國家有關(guān)臨床試驗(yàn)的法律法規(guī)，具有獨(dú)立的醫(yī)學(xué)研究能力。
5.具備敏銳的市場(chǎng)洞察力；具有很強(qiáng)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.
