雇員點(diǎn)評標(biāo)簽
職位描述
臨床數(shù)據(jù)分析生物工程
崗位職責(zé):
Able to conduct data management daily works independently, including DM documents preparation, coding, query management, maunal review and other DM related activies.
? Responsible for ensuring the completeness, quality and integrity of the subject data in the clinical trial database.
? Ensure the consistent use and application of applicable data standards. The ultimate objective is to ensure data quality and consistency across programs and repositories.
? Responsible for data management activities within a clinical trial, according to regulations, applicable Standard Operating Procedures (SOPs) and Processes.
? Works with the global study team to meet the study objectives.
JD: For Hands-on data management (Data Manager)
? Create and implement the Data Management Plans (DMP) to ensure data completeness and accuracy.
? Set-up and test data review listings to verify the quality and completeness of data as specified in DMP.
? Ensure timely set-up of clinical data acquisition and management tools and data validation.
? Maintain study tracking to ensure timely CRF retrieval, data entry and data cleaning activities.
? Perform data cleaning activities including discrepancy management (review of errors from electronic checks) and review of data listings to verify quality and completeness of data.
? Ensure integrity of clinical data and update database by issuing and resolving DCFs as necessary.
? Reconcile the patient database with the Serious Adverse Event database.
? Document all efforts of data management and file all responsible documents.
任職要求:
At least 1 to 2 years full time work experience as DM focus on drug trial.
? Bachelor degree or above
? Have basic sense of ICH-GCP.
? Smart and quick to catch up. Have good capability in self-learning, communication and planning.
? Better to have experience in global pharmaceutical company studies
? Better to have strategic thinking and risk management sense.
Be capable of working under high pressure
Requirement on EN
? Listening-able to take EN training and meetings
? Speaking-able to communicate with EN speaking people clearly
? Reading-able to read EN protocol and academic materials
? Writing-able to write EN e-mails and reports
職位福利：五險一金、交通補(bǔ)助、餐補(bǔ)、帶薪年假、補(bǔ)充醫(yī)療保險、定期體檢、高溫補(bǔ)貼、節(jié)日福利
工作地點(diǎn)
上海長寧區(qū)華聞國際大廈
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程紅/招聘
昨日活躍立即溝通
泰格醫(yī)藥
泰格醫(yī)藥(股票代碼:300347.SZ/3347.HK)是行業(yè)領(lǐng)先的一體化生物醫(yī)藥研發(fā)服務(wù)平臺，為全球制藥和醫(yī)療器械行業(yè)提供跨越全周期的臨床研究創(chuàng)新解決方案。通過全面的服務(wù)體系和頂尖的質(zhì)量標(biāo)準(zhǔn)，我們助力生物醫(yī)藥產(chǎn)業(yè)提升研發(fā)效率、降低研發(fā)風(fēng)險，確保研究項(xiàng)目高質(zhì)量交付，加速醫(yī)藥產(chǎn)品市場化進(jìn)程，履行對行業(yè)和患者的承諾。同時，我們也通過覆蓋各領(lǐng)域的 100多家子公司，打造賦能全產(chǎn)業(yè)鏈的創(chuàng)新生態(tài)，推動醫(yī)療產(chǎn)業(yè)創(chuàng)新和發(fā)展。作為全球化的研發(fā)平臺，泰格醫(yī)藥在全球布局 180多個辦事處和分支機(jī)構(gòu)，擁有超過 9500人的專業(yè)團(tuán)隊(duì)，覆蓋5大洲的 54個國家，致力于解決最具挑戰(zhàn)的全球健康問題，滿足患者的未盡醫(yī)療需求，創(chuàng)造社會價值，造福人類健康。更多詳情請登錄：http://tigermed.zhiye.com/或?qū)⒛暮啔v發(fā)送至：TA@tigermedgrp.com（請務(wù)必在郵件主題中注明：意向地區(qū)+意向崗位+姓名）
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