- 目錄
崗位職責(zé)是什么
臨床數(shù)據(jù)崗位是醫(yī)療健康行業(yè)中至關(guān)重要的角色，主要負責(zé)收集、整理、分析和管理與臨床試驗相關(guān)的大量數(shù)據(jù)，以支持醫(yī)療研究、新藥開發(fā)和患者治療決策。
崗位職責(zé)要求
1. 具備扎實的醫(yī)學(xué)基礎(chǔ)知識，熟悉臨床試驗流程及法規(guī)。
2. 精通數(shù)據(jù)分析工具，如sas、r、python等，能處理大規(guī)模數(shù)據(jù)。
3. 嚴謹細心，確保數(shù)據(jù)準確無誤，遵守數(shù)據(jù)保護和隱私法規(guī)。
4. 良好的溝通協(xié)調(diào)能力，與研究團隊、醫(yī)療專家及監(jiān)管機構(gòu)有效協(xié)作。
5. 掌握項目管理技巧，能在多任務(wù)環(huán)境下高效工作。
崗位職責(zé)描述
臨床數(shù)據(jù)專員的工作涉及多個環(huán)節(jié)，從設(shè)計數(shù)據(jù)收集方案，到實施數(shù)據(jù)錄入、清理和驗證，再到生成統(tǒng)計報告，每一個步驟都需要精確無誤。他們需要理解和解讀復(fù)雜的醫(yī)學(xué)文獻，確保臨床試驗數(shù)據(jù)的科學(xué)性和可靠性。此外，他們還需與跨學(xué)科團隊密切合作，解決數(shù)據(jù)問題，確保研究進度順利進行。
有哪些內(nèi)容
1. 數(shù)據(jù)管理：制定數(shù)據(jù)標準，建立數(shù)據(jù)庫，進行數(shù)據(jù)錄入、校驗和管理。
2. 數(shù)據(jù)分析：運用統(tǒng)計學(xué)方法對數(shù)據(jù)進行深度分析，發(fā)現(xiàn)潛在模式和趨勢。
3. 報告撰寫：編寫詳細的臨床研究報告，呈現(xiàn)數(shù)據(jù)分析結(jié)果，供決策參考。
4. 項目協(xié)調(diào)：參與臨床試驗項目的規(guī)劃和執(zhí)行，確保數(shù)據(jù)質(zhì)量和合規(guī)性。
5. 問題解決：針對數(shù)據(jù)異?；驙幾h，與研究團隊共同尋找解決方案。
6. 持續(xù)學(xué)習(xí)：關(guān)注醫(yī)療領(lǐng)域最新發(fā)展，提升數(shù)據(jù)分析技能，適應(yīng)不斷變化的行業(yè)需求。
臨床數(shù)據(jù)崗位的工作是醫(yī)療創(chuàng)新的關(guān)鍵一環(huán)，通過精準的數(shù)據(jù)處理和分析，推動新療法的研發(fā)，改善患者預(yù)后，為醫(yī)療行業(yè)的進步貢獻力量。
臨床數(shù)據(jù)崗位職責(zé)范文
第1篇 臨床數(shù)據(jù)分析員崗位職責(zé)
臨床數(shù)據(jù)分析員 江蘇恩華藥業(yè)股份有限公司 江蘇恩華藥業(yè)股份有限公司,恩華藥業(yè),江蘇恩華藥業(yè),恩華 崗位職責(zé):
1. 負責(zé)新藥臨床研究項目數(shù)據(jù)的統(tǒng)計與分析工作,收集整理臨床診療數(shù)據(jù)并進行挖掘分析;
2. 參與臨床試驗方案設(shè)計:試驗設(shè)計、樣本量計算、終點指標及其分析方法的選擇;
3. 獨立撰寫統(tǒng)計分析計劃;撰寫統(tǒng)計分析報告;
4. 負責(zé)和管理項目進度,以及程序相關(guān)的問題溝通;
5. 其他相關(guān)的統(tǒng)計分析。
任職要求:
1. 流行病與衛(wèi)生統(tǒng)計學(xué)、生物統(tǒng)計學(xué)、計算機、數(shù)學(xué)及相關(guān)專業(yè),碩士研究生;
2. 獨立完成過臨床數(shù)據(jù)收集、整理、挖掘分析工作;熟悉臨床試驗設(shè)計與統(tǒng)計分析流程,熟練使用sas、stata、spss,prismgraphpad等統(tǒng)計軟件和畫圖軟件;
3. 一年以上大型cro或藥廠臨床試驗sas程序員工作經(jīng)驗者優(yōu)先。
4. cet6,英語聽說讀寫能力良好;
5. 熱愛生物醫(yī)學(xué)數(shù)據(jù)分析工作,邏輯思維強,具備優(yōu)秀的團隊合作能力和獨立解決問題的能力。
第2篇 臨床數(shù)據(jù)經(jīng)理崗位職責(zé)
臨床數(shù)據(jù)經(jīng)理 primary activities include, but are not limited to:
? all responsibilities of a clinical data manager.
? assume data management responsibilities for larger, more comple_ or higher priority protocols.
? may coordinate general ad-hoc sponsor data entry (sde) process for the protocol, discuss timelines, and provide data entry status to the clinical development scientist (cds).
? provide protocol specific training of sde process to cdm.
? triage, research, discuss and resolve the reports outputs provided by clinical development scientist (cds) and statisticians at a protocol level during in-life and database lock stages supported by the lcdm.
? supports the lcdm in the preparation, creation and review of data management tool specifications and tools
? participates in user acceptance testing (uat) of the clinical database repository under the direction of the lcdm.
? coordinates communications, global status tracking and issue resolution at study level with lead cdm (lcdm).
? responsible for the communication with clinical trial operations team regarding site level issues on protocol a basis on behalf of the lcdm.
? monitor protocol level cycle time performance (metrics) and follow up on specific countries/sites metrics issues and deliver status and resolution updates to lcdm.
? responsible for study level status assessment, reporting and communication with lcdm.
? complete trial level archiving activities under the direction of the lcdm including, but not limited to, filing of essential documentation.
? coordinate and mentor cdms and other scdms who work in his/ her protocol to ensure their compliance with sops, data management plans and data review plans.
? be assigned to special responsibilities related to process maintenance, data quality assessment, staff training and mentoring and/ or other special activities, such as providing inputs to create or update sops, supporting documents and training materials as needed.
? may be required to support dmc process owner (po) models in the local dmc and/or in the global po networks.
? participate in cross functional technical or process improvement projects.
manual encoding lead
? perform all responsibilities of a manual encoder under the clinical data manager.
? ensure encoding accuracy and consistency across all protocols within a project.
? works closely with dmc manual encoders and data management trial manager (dmtm) to ensure all encoding tasks are completed prior to interim analysis, frozen files/ database locks.
? serves as subject matter e_pert (sme) for encoding documents and processes.
? responsible to review specified therapeutic area encoding as requested.
? coordinates with lcdm to create and review encoding specifications documents and performs user acceptance testing (uat) of coding application (s).
? responsible for encoding e_ternal partner data as applicable and consultant for contract research organization (cro) partners.
? runs encoding check reports in accordance with data review plans to identify encoding issues.
? raises questions with investigational site staff or dmc manual encoders and reviews responses and corresponding data corrections to confirm resolution.
? responsible for study level encoding status reporting and assessment, and communication with dmc clinical trial (ct) management during in-life data management activities and preparation for database lock.
requirements
education:
1. at least b.a. or b.s. degree, preferably in medicine, pharmacy, nursing, biological sciences, or health care related discipline.
knowledge and skills:
1. two years’ e_perience in clinical data management in pharmaceutical or health care clinical research environment is preferable.
2. self-motivated, e_cellent in work planning and time management.
3. fluent oral and written english skills.
4. good basic awareness of the clinical development process.
5. good basic awareness of clinical practice and grasp of medical terminology.
6. good sense and awareness of regulations and policies.
7. able to work under pressure and in a changing environment with fle_ibility.
8. good communication skills with the ability to communicate with both technical and business areas.
9. proven leadership skills, specifically the ability to coordinate the work of others and influence management on decision making. primary activities include, but are not limited to:
? all responsibilities of a clinical data manager.
? assume data management responsibilities for larger, more comple_ or higher priority protocols.
? may coordinate general ad-hoc sponsor data entry (sde) process for the protocol, discuss timelines, and provide data entry status to the clinical development scientist (cds).
? provide protocol specific training of sde process to cdm.
? triage, research, discuss and resolve the reports outputs provided by clinical development scientist (cds) and statisticians at a protocol level during in-life and database lock stages supported by the lcdm.
? supports the lcdm in the preparation, creation and review of data management tool specifications and tools
? participates in user acceptance testing (uat) of the clinical database repository under the direction of the lcdm.
? coordinates communications, global status tracking and issue resolution at study level with lead cdm (lcdm).
? responsible for the communication with clinical trial operations team regarding site level issues on protocol a basis on behalf of the lcdm.
? monitor protocol level cycle time performance (metrics) and follow up on specific countries/sites metrics issues and deliver status and resolution updates to lcdm.
? responsible for study level status assessment, reporting and communication with lcdm.
? complete trial level archiving activities under the direction of the lcdm including, but not limited to, filing of essential documentation.
? coordinate and mentor cdms and other scdms who work in his/ her protocol to ensure their compliance with sops, data management plans and data review plans.
? be assigned to special responsibilities related to process maintenance, data quality assessment, staff training and mentoring and/ or other special activities, such as providing inputs to create or update sops, supporting documents and training materials as needed.
? may be required to support dmc process owner (po) models in the local dmc and/or in the global po networks.
? participate in cross functional technical or process improvement projects.
manual encoding lead
? perform all responsibilities of a manual encoder under the clinical data manager.
? ensure encoding accuracy and consistency across all protocols within a project.
? works closely with dmc manual encoders and data management trial manager (dmtm) to ensure all encoding tasks are completed prior to interim analysis, frozen files/ database locks.
? serves as subject matter e_pert (sme) for encoding documents and processes.
? responsible to review specified therapeutic area encoding as requested.
? coordinates with lcdm to create and review encoding specifications documents and performs user acceptance testing (uat) of coding application (s).
? responsible for encoding e_ternal partner data as applicable and consultant for contract research organization (cro) partners.
? runs encoding check reports in accordance with data review plans to identify encoding issues.
? raises questions with investigational site staff or dmc manual encoders and reviews responses and corresponding data corrections to confirm resolution.
? responsible for study level encoding status reporting and assessment, and communication with dmc clinical trial (ct) management during in-life data management activities and preparation for database lock.
requirements
education:
1. at least b.a. or b.s. degree, preferably in medicine, pharmacy, nursing, biological sciences, or health care related discipline.
knowledge and skills:
1. two years’ e_perience in clinical data management in pharmaceutical or health care clinical research environment is preferable.
2. self-motivated, e_cellent in work planning and time management.
3. fluent oral and written english skills.
4. good basic awareness of the clinical development process.
5. good basic awareness of clinical practice and grasp of medical terminology.
6. good sense and awareness of regulations and policies.
7. able to work under pressure and in a changing environment with fle_ibility.
8. good communication skills with the ability to communicate with both technical and business areas.
9. proven leadership skills, specifically the ability to coordinate the work of others and influence management on decision making.
第3篇 臨床數(shù)據(jù)崗位職責(zé)
醫(yī)學(xué)數(shù)據(jù)分析師 hitales 上海翼依信息技術(shù)有限公司,hitales,上海翼依,翼依,翼依科技,翼依 跟隨國內(nèi)知醫(yī)療信息學(xué)副教授,參與醫(yī)療人工智能項目。
醫(yī)學(xué)數(shù)據(jù)分析專員
崗位職責(zé)
1、負責(zé)醫(yī)學(xué)相關(guān)臨床數(shù)據(jù)的整理、分析工作,參與醫(yī)學(xué)相關(guān)知識圖譜構(gòu)建;
2、負責(zé)相關(guān)數(shù)據(jù)產(chǎn)品和治療領(lǐng)域的醫(yī)學(xué)文獻的檢索整理;
3、參與醫(yī)學(xué)大數(shù)據(jù)挖掘、分析工作;
4、參與公司醫(yī)療相關(guān)產(chǎn)品的需求收集、整理、分析;產(chǎn)品規(guī)劃、設(shè)計等工作;
5、參與公司醫(yī)學(xué)相關(guān)知識架構(gòu)搭建及內(nèi)容完善工作;
6、 負責(zé)查閱、收集國內(nèi)外臨床試驗信息,掌握臨床試驗領(lǐng)域的發(fā)展趨勢;
7、協(xié)助開展相關(guān)領(lǐng)域的調(diào)研,為產(chǎn)品優(yōu)化提供科學(xué)依據(jù)。
任職資格:
1、臨床醫(yī)學(xué)、基礎(chǔ)醫(yī)學(xué)、公共衛(wèi)生、藥學(xué)等醫(yī)學(xué)相關(guān)專業(yè)本科畢業(yè);
2、2年以上醫(yī)學(xué)數(shù)據(jù)分析工作經(jīng)驗
3、具有醫(yī)學(xué)臨床決策支持算法與系統(tǒng)構(gòu)建經(jīng)驗、有互聯(lián)網(wǎng)與人工智能相關(guān)工作經(jīng)驗者優(yōu)先考慮;
4、良好的溝通能力和團隊合作精神;
5、為人謹慎,細致工作負責(zé);
第4篇 臨床數(shù)據(jù)分析崗位職責(zé)
臨床數(shù)據(jù)分析 樂普 樂普(北京)醫(yī)療器械股份有限公司,樂普,樂普醫(yī)療,樂普醫(yī)療器械,樂普醫(yī)療集團,樂普移動醫(yī)療,北京樂普,樂普 職責(zé)描述:
1、熟悉臨床分析軟件;
2、在一定時間內(nèi)收集、整理和核查(邏輯核查及醫(yī)學(xué)核查)臨床試驗數(shù)據(jù);
3、確保臨床試驗數(shù)據(jù)的完整性、準確性和內(nèi)部數(shù)據(jù)庫的一致性,使其符合報告至管理機構(gòu)的質(zhì)量標準;
4、與臨床監(jiān)察員和研究者就臨床報告管理工作進行密切溝通及協(xié)調(diào)。
任職要求:
1、醫(yī)學(xué)統(tǒng)計或相關(guān)專業(yè)本科及以上學(xué)歷;
2、使用過sas、spss、e_cel等統(tǒng)計分析工具;
3、良好的溝通能力及語言表達能力;
4、符合以下條件者優(yōu)先:有edc的使用經(jīng)驗;有臨床數(shù)據(jù)管理經(jīng)驗,有cra或crc工作經(jīng)驗,有oracle database,sql使用和編程經(jīng)驗者優(yōu)先;
第5篇 臨床數(shù)據(jù)分析師崗位職責(zé)
臨床數(shù)據(jù)分析師 上海森億醫(yī)療科技有限公司 上海森億醫(yī)療科技有限公司,森億智能,森億 職位描述:
1.根據(jù)項目需求,撰寫統(tǒng)計分析計劃書,獨立完成各類型的臨床研究的統(tǒng)計分析工作;
2.參與產(chǎn)品統(tǒng)計模塊的功能設(shè)計和測試;
3.根據(jù)產(chǎn)品、應(yīng)用方向,對醫(yī)療大數(shù)據(jù)整體進行統(tǒng)計分析及數(shù)據(jù)挖掘;
4.對內(nèi)部及外部進行統(tǒng)計培訓(xùn)、項目介紹 。
職位要求:
1.衛(wèi)生統(tǒng)計、流行病學(xué)、統(tǒng)計學(xué)、應(yīng)用統(tǒng)計等相關(guān)專業(yè)背景,碩士及以上學(xué)歷; 至少1年以上統(tǒng)計師、sas programmer、醫(yī)療行業(yè)數(shù)據(jù)分析等相關(guān)工作經(jīng)驗;
2.從事臨床試驗統(tǒng)計分析者優(yōu)先,有醫(yī)療/健康數(shù)據(jù)分析及建模的經(jīng)驗優(yōu)先;
3.熟悉醫(yī)學(xué)研究相關(guān)的統(tǒng)計方法;熟練掌握至少一門統(tǒng)計編程軟件:sas、r、python;
4.熟練使用sas或r繪制符合行業(yè)標準的統(tǒng)計表格和統(tǒng)計圖;
5.有醫(yī)藥企業(yè)或cro公司撰寫統(tǒng)計分析計劃書(sap)經(jīng)驗優(yōu)先;
6.熟悉臨床研究思路、方案設(shè)計、樣本量計算等;
7.良好的學(xué)習(xí)能力、邏輯思維和語言表達能力。
第6篇 臨床數(shù)據(jù)助理崗位職責(zé)
臨床數(shù)據(jù)管理助理 佰榮泰華 北京佰榮泰華生物醫(yī)藥科技有限公司,佰榮泰華,佰榮泰華 崗位職責(zé):
1、參與數(shù)據(jù)管理人工核查等工作;
2、配合數(shù)據(jù)管理員進行數(shù)據(jù)質(zhì)疑等工作;
3、協(xié)助數(shù)據(jù)管理專員完成工作;
4、領(lǐng)導(dǎo)交辦的其他任務(wù);
任職要求:
1、專科以上學(xué)歷;
2、工作細心踏實,責(zé)任心強;
3、能承擔(dān)重復(fù)的工作;
4、有發(fā)現(xiàn)錯誤的敏感度;
5、有團隊溝通和協(xié)調(diào)能力;
6、能熟練使用辦公軟件;
