• 3-4年经验
  • 本科
  • 招1人
  • 02-24 发布

职位描述

About Our ClientCARsgen therapeutics is a clinical-stage immunotherapy company with a focus to develop and commercialize novel chimeric antigen receptor T-cell (CAR-T) therapeutics. The main goal is to harness our propriety and state-of-the-art CAR-T therapy to fight against tumor with a perspective to cure cancer, improving people's life quality and reducing associated suffering. Gathered by a group of world-class scientists, CARsgen has developed World's first-in-class CAR-T candidate for hepatocellular carcinoma and China's exclusive candidate for glioblastoma multiform.As a global innovator in CAR-T therapies for solid tumor treatment, CARsgen Therapeutics has proven itself by initiating the world's first CAR-T clinical trial on HCC (hepatocellular carcinoma) and leading trial on GBM (glioblastoma).With outstanding expertise in cancer research, CARsgen generates, develops, establishes various proprietary technology and patents, boosting a broad CAR-T portfolio covering most solid and blood tumors. Some candidate products are world-leading.Job DescriptionResponsible for the clinical feasibility of product development and clinical trial protocol design and draftResponsible for medical and scientific support for clinical trial such as the draft, review and modification on medical chart, CRF, ICF, patient diary, IB. etcResponsible for the draft, review and modification on Clinical Study Report, clinical study summary, and other clinical data submission materialsCommunicate with medical experts and CDE experts according to the requirement of clinical trialsParticipate in investigator meeting and provide scientific supportProvide scientific support for product regulatory submission and clinical trialsResponsible for interpreting the efficacy and safety dataThe Successful ApplicantBachelor degree or above in Medical, Pharmacology or Biology related major.3-5 years medical writing experiences, and experience as medical manager in pharmaceutical companies preferred. Strong medical editor background and good at medical information retrieval and reading.Familiar with the properties of products and clinical trials on different therapeutic areasCapable of communicating with experts from clinical trial sites and CFDAFluent in both written and oral EnglishGood command of Microsoft offices.What's on OfferAttractive salary packageBuild up your career within the great platformRich space for development and promotionContact: Jay Jay LiQuote job ref: 3974143+86 21 6157 5089 职能类别: 医药技术研发管理人员

联系方式

南京西路1539号静安嘉里中心办公楼二座11楼

公司信息

米高蒲志是全球领先的专业招聘顾问公司,专精于为全球知名雇主招募全职、约聘与临时职位。集团在35个国家设有155个办事处。自1976年在伦敦成立以来,三十多年来我们一直致力与为求职者和雇主牵线搭桥。我们在伦敦证券交易所挂牌上市,每年的营业额超过10亿美元。 目前我们在全球所有主要商业中心设有办事处,包括:中国香港,伦敦, 纽约, 巴黎, 东京, 多伦多, 新加坡, 悉尼。 2003年,我们在上海开办了第一个办事处。我们在中国大陆地区的办公室地点:北京, 上海(浦东与浦西), 苏州, 深圳以及广州。我们专注的招聘领域包括以下13个领域:• 财务与会计• 金融服务与银行• 工程与制造• 人力资源• 信息技术• 法律• 市场营销• 数字营销与电子商务• 房地产与建筑• 采购与供应链• 零售与采购• 销售• 办公室行政与助理

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