日日噜夜夜草|一级黄色录像高清版|调教白富美加勒比久久|亚洲欧洲精品婷婷|日韩综合无码色色|日韩精品一区妖精视频|亚洲无码中文字幕hd|99亚洲思思丝袜|手机看片国产精品大胆亚洲|成人无码视频一区二区在线播放

更新于 4月9日

(高級)醫(yī)學(xué)顧問-抗感染疾病領(lǐng)域

2.5-3萬
  • 上海靜安區(qū)
  • 1-3年
  • 碩士
  • 全職
  • 招1人

雇員點評標(biāo)簽

  • 同事很nice
  • 團(tuán)隊執(zhí)行強(qiáng)
  • 工作環(huán)境好
  • 人際關(guān)系好
  • 氛圍活躍
  • 實力大公司

職位描述

生物藥
Main Responsibilities: Antimicrobial & Antifungal Stewardship (AMS & AFS): Advocate for the rational use of antimicrobial agents in clinical practice by optimizing AMS and AFS systems and generating relevant medical evidence. - Develop and refine AMS/AFS strategies in alignment with national and regional antimicrobial management policies, guidelines, and data from antimicrobial surveillance networks. - Investigate the clinical use of antimicrobial agents through real-world data, assess the impact of AMS/AFS strategies on patient outcomes, disease management, and healthcare costs, and provide evidence-based support for the rational of antimicrobials. - Optimize AMS/AFS strategies to various clinical scenarios based on real-world evidence, aiming to enhance the quality of antimicrobial application and reduce the risk of resistance. Quality Improvement (QI) in Antimicrobial Clinical Application: Identify and address common challenges in the clinical use of antimicrobial agents by analyzing relevant diagnostic and therapeutic processes to highlight significant issues and propose constructive solutions to improve the quality of antimicrobial application. - Understand the standards in the diagnosis and treatment of infectious diseases (ID), and develop and optimize QI strategies for the clinical application of antimicrobial agents based on unmet needs, ensuring that the standards align with advancements in the field of ID and meet clinical requirements. - Evaluate the effectiveness of antimicrobial clinical applications based on the implementation of QI strategies, and conduct regular assessments to ensure the sustainability of quality improvement measures. - Integrate the resources in the ID field to create a comprehensive medical activity platform that enhances academic influence and resource sharing. - Monitor national healthcare policies, including Value-Based Purchasing (VBP) and Diagnosis-Related Groups (DRG), and provide necessary medical support in the field of infections as required. ID products Lifecycle Management: Provide comprehensive medical support for both early- and late-stage infection products, ensuring the medical guidance and support are available at all stages of the product lifecycle to promote product development. - Support BD assessments in ID field, ensuring scientific validity of product assessment. - Prepare for and provide medical support for ID products that are over 3 years from commercial launch, establishing a foundation for successful product launches. - Provide necessary medical support as needed for late-stage infection products, such as CSO products. Required skills Must-possess: - Therapeutic area knowledge: familiar with the disease knowledge and clinical practice of the therapeutic area - Quick Learning: Ability to master advancements in the global medical field. - Project Management: Demonstrated ability to manage projects effectively, including proactive planning, resource coordination, risk management, and ensuring high-quality outcomes. - Efficient Execution: Capacity to quickly grasp task requirements and effectively address implementation challenges. - Interpersonal Communication: Strong communication skills to engage effectively with diverse stakeholders at various levels. - Strategic Thinking: Ability to think strategically and analyze complex situations critically. - Team Collaboration: A collaborative spirit with a commitment to working effectively within a team. - Language Proficiency: Fluent in English (both spoken and written) is essential. Preferred: - Clinical Trial Knowledge: Basic understanding of clinical trial processes. - Customer Orientation: A strong focus on meeting customer needs and delivering high-quality medical services. - Business Acumen: possess strong business insight Educational Background: Master degree or above in medicine, pharmacology or relevant therapeutic area. Work Experience: - Experience as a clinical physician. - Minimum of 2 years of experience in the pharmaceuticals. Previous Experience in medical affairs is preferred. Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Medical #LI-PFE

工作地點

上海靜安區(qū)中信泰富廣場

職位發(fā)布者

劉一飛/人事經(jīng)理

當(dāng)前在線
立即溝通
公司Logo輝瑞投資有限公司公司標(biāo)簽
輝瑞公司(Pfizer Inc.)創(chuàng)建于1849年,總部位于美國紐約,是一家以科學(xué)為基礎(chǔ)的、創(chuàng)新的、以患者為先的生物制藥公司。輝瑞的使命是“為患者帶來改變其生活的突破創(chuàng)新”。在輝瑞,我們通過科學(xué)和全球資源為人們提供治療方案,以延長其生命,顯著改善其生活。在醫(yī)療衛(wèi)生產(chǎn)品的探索、研發(fā)和生產(chǎn)過程中,輝瑞始終致力于奉行嚴(yán)格的質(zhì)量、安全和價值標(biāo)準(zhǔn)。我們在全球的產(chǎn)品組合包括創(chuàng)新藥品和疫苗。每天,輝瑞在發(fā)達(dá)和新興市場的員工都在推進(jìn)人類健康,推動疾病的預(yù)防、治療和治愈,以應(yīng)對挑戰(zhàn)我們這個時代的頑疾。輝瑞還與醫(yī)療衛(wèi)生服務(wù)方、政府和社區(qū)合作,支持并促進(jìn)世界各地的人們能夠獲得更為可靠和可承付的醫(yī)療衛(wèi)生服務(wù)。這與輝瑞作為一家全球卓越的創(chuàng)新生物制藥公司的責(zé)任是一致的。170余年來,輝瑞一直致力于為所有依賴我們的人帶來改變。輝瑞于1989年進(jìn)入中國市場。扎根中國30余年,輝瑞已成為在華主要的外資制藥公司之一。2021年是輝瑞新征程的開始。迄今已有170余年歷史的輝瑞正在邁入全新時代,成為一家以科學(xué)為基礎(chǔ)的、創(chuàng)新的、以患者為先的生物制藥公司。目前輝瑞在中國業(yè)務(wù)覆蓋全國300余個城市,累計投資超過15億美元,并設(shè)立了1家先進(jìn)的生產(chǎn)設(shè)施,2個研發(fā)中心(分別位于上海張江高科技園區(qū)和武漢光谷),在華有近7,000名員工分布于業(yè)務(wù)、研發(fā)和生產(chǎn)等領(lǐng)域。輝瑞在華上市了五大領(lǐng)域的高品質(zhì)創(chuàng)新產(chǎn)品,包括腫瘤、疫苗、抗感染、炎癥與免疫、罕見病等多個領(lǐng)域的處方藥和疫苗,強(qiáng)大完善的產(chǎn)品線旨在滿足生命各階段的健康需求。
公司主頁