臨床專員崗位職責16篇

第1篇 臨床醫(yī)學專員崗位職責

臨床醫(yī)學專員/經理 職位描述:

1.根據臨床試驗要求,負責設計及報告撰寫階段的文獻檢索查詢相關醫(yī)學、藥信息和參考文獻,提供相關信息;

2.參與臨床試驗方案討論,撰寫或修改、病例報告表知情同意書等;

3.負責臨床研究總結報告的撰寫;

4.協助商務部門項目投標的醫(yī)學支持、臨床試驗研究方案摘要等相關文件撰寫。

任職要求 :

1.臨床醫(yī)學 、藥相關專業(yè)碩士學 歷,有醫(yī)學撰寫經驗者優(yōu)先;

2.英語讀寫流利,能夠熟練閱和翻譯醫(yī)學、藥方面專業(yè)文獻;

3.能夠熟練使用醫(yī)學、藥專業(yè)文獻檢索工具;

4. 善于溝通,具有良好的團隊合作精神。 職位描述:

1.根據臨床試驗要求,負責設計及報告撰寫階段的文獻檢索查詢相關醫(yī)學、藥信息和參考文獻,提供相關信息;

2.參與臨床試驗方案討論,撰寫或修改、病例報告表知情同意書等;

3.負責臨床研究總結報告的撰寫;

4.協助商務部門項目投標的醫(yī)學支持、臨床試驗研究方案摘要等相關文件撰寫。

任職要求 :

1.臨床醫(yī)學 、藥相關專業(yè)碩士學 歷,有醫(yī)學撰寫經驗者優(yōu)先;

2.英語讀寫流利,能夠熟練閱和翻譯醫(yī)學、藥方面專業(yè)文獻;

3.能夠熟練使用醫(yī)學、藥專業(yè)文獻檢索工具;

4. 善于溝通,具有良好的團隊合作精神。

第2篇 臨床信息專員崗位職責任職要求

臨床信息專員崗位職責

臨床信息專員 1、客訴信息的接受、跟蹤、了解、分析。

2、客訴問題和各部門及時溝通，在臨床角度給出產生客訴的可能

3、審查客訴診斷報告并給出到相關人員

4、必要時和客戶見面了解信息，給出客訴診斷。

5、在產品立項、研究等情況時，給出相關臨床意見

6、跟蹤新產品的動物實驗、臨床試驗，試用、使用情況，并給出意見。

7、參與質量改善，給出臨床方面意見

8、完成宣傳產品等其他相關任務。

要求10年以上外科醫(yī)生經驗，崗位相當于技術顧問，從醫(yī)生的角度給產品指導及根據反饋給出合理建議 1、客訴信息的接受、跟蹤、了解、分析。

2、客訴問題和各部門及時溝通，在臨床角度給出產生客訴的可能

3、審查客訴診斷報告并給出到相關人員

4、必要時和客戶見面了解信息，給出客訴診斷。

5、在產品立項、研究等情況時，給出相關臨床意見

6、跟蹤新產品的動物實驗、臨床試驗，試用、使用情況，并給出意見。

7、參與質量改善，給出臨床方面意見

8、完成宣傳產品等其他相關任務。

要求10年以上外科醫(yī)生經驗，崗位相當于技術顧問，從醫(yī)生的角度給產品指導及根據反饋給出合理建議

臨床信息專員崗位

第3篇 臨床維護專員崗位職責

崗位職責:負責客情關系的維護工作;負責產品的進一步講解和臨床銷售;負責其余科室的宣傳維護工作;崗位要求:有過相關工作經驗者優(yōu)先,并且待遇優(yōu)厚!學醫(yī)或從事護理專業(yè)方面的優(yōu)先!

第4篇 cra臨床研究專員崗位職責

臨床研究專員/cra- 上海 達孜縣君合科技有限公司 達孜縣君合科技有限公司,君合醫(yī)藥,君合科技,君合 職位描述:

按照要求協助或負責i~iv 期臨床研究中的各項工作,對新藥研發(fā)流程及臨床研究相關法律法規(guī)有一定了解。在臨床研究經理或項目經理指導下,能夠負責研究中心的日常管理工作,獨立進行監(jiān)查工作。

任職資格:

1. 臨床醫(yī)學、藥學或相關專業(yè)學歷,對藥品管理有關法規(guī)、臨床研究和臨床研究監(jiān)查流程有一定了解。

2. 一年以上臨床研究監(jiān)查工作經驗,進行過獨立的臨床研究監(jiān)查。

3. 具備一定的溝通表達能力、判斷能力、應變能力及問題解決能力。

4. 良好的寫作能力及組織能力,能夠根據工作分配的強度及優(yōu)先度進行自我調整。

5. 積極主動的工作態(tài)度,能適應長期出差。

6. 熟練的使用windows操作系統(tǒng)與office系列辦公軟件包括word、e_cel、powerpoint。

7. 具備一定的英語閱讀及寫作能力。

第5篇 臨床專員崗位職責

臨床專員 博毅雅(上海)醫(yī)療科技有限責任公司 博毅雅(上海)醫(yī)療科技有限責任公司,博毅雅 工作職責:

1、 為客戶或部門內部提供產品知識培訓及臨床應用培訓;

2、 協助產品推廣,向用戶現場演示和介紹產品、臨床應用的方法;

3、 收集臨床資料和用戶需求反饋,研究總結臨床應用優(yōu)勢和新的產品應用領域。

4、 幫助銷售人員和代理商更好地理解產品的臨床應用。

5、 與國內、國外的業(yè)內專家建立聯系,為公司產品開發(fā)提供臨床理論支持。

任職資格:

1、具有醫(yī)學背景及臨床實踐背景;

2、善于溝通,有應急事件處理能力,高度的責任感及對外協調能力。

3、較強的學習能力和上進心心。

第6篇 臨床協調專員崗位職責

cra(臨床試驗協調專員) 欣凱醫(yī)藥化工中間體 欣凱醫(yī)藥化工中間體(上海)有限公司,欣凱醫(yī)藥,欣凱醫(yī)藥化工中間體,欣凱 崗位職責:

1.根據gcp及公司sop執(zhí)行臨床監(jiān)查工作;

2.確保試驗嚴格按照方案、gcp及相關法律法規(guī)執(zhí)行;

3.協助研究中心解決試驗過程中可能出現的問題;

4.確保研究數據及時、準確、完整地記錄在原始病歷中,病例報告表與原始病歷數據一致;

5.及時全面地匯報研究中心進展情況;

6.完成相應書面工作;

7.協助研究者及時完成數據疑問;

8.及時、完整地收集研究相關資料;

9.完成試驗結束階段的藥品、資料整理與回收,關閉中心。

任職要求:

1. 臨床醫(yī)學、藥學等相關專業(yè)本科及本科以上學歷;有臨床風濕病工作經驗優(yōu)先;

2. 一年以上臨床監(jiān)查工作經驗;

3. 熟悉臨床試驗監(jiān)查、fda、cfda法規(guī)、ich/gcp條例;

4.與人溝通、談判、表達能力較強。

第7篇 臨床銷售專員崗位職責任職要求

臨床銷售專員崗位職責

【長沙_臨床微生物】客戶專員/銷售代表 responsibility:

-sales targets: actively complete assigned territory core instrument/reagent business sales tasks through field clinical communication in relevant departments of hospitals

-customer management: implement field clinical communication and utilize the bd academic platform and the speaker pools to influence the customers in territory for business.

-strictly abide by country compliance law and bd policy and rules.

-visit target customers regularly according to the specified scope and do the micro-market analysis for the assigned hospitals. target customer includes clinical laboratory director， micro-biology team leader， relevant clinical department doctors and nurses， infection & control department director， equipment director， vice president and president.

- make sales/marketing strategy against competitors together with marketing and as team.

-be participant into professional education branding establishment of ds， enhance self-capabilities， especially on knowledge of microbiology， to be an e_pert in microbiology industrial. responsibility:

-sales targets: actively complete assigned territory core instrument/reagent business sales tasks through field clinical communication in relevant departments of hospitals

-customer management: implement field clinical communication and utilize the bd academic platform and the speaker pools to influence the customers in territory for business.

-strictly abide by country compliance law and bd policy and rules.

-visit target customers regularly according to the specified scope and do the micro-market analysis for the assigned hospitals. target customer includes clinical laboratory director， micro-biology team leader， relevant clinical department doctors and nurses， infection & control department director， equipment director， vice president and president.

- make sales/marketing strategy against competitors together with marketing and as team.

-be participant into professional education branding establishment of ds， enhance self-capabilities， especially on knowledge of microbiology， to be an e_pert in microbiology industrial.

臨床銷售專員崗位

第8篇 臨床協調專員崗位職責任職要求

臨床協調專員崗位職責

崗位職責:

1.根據gcp及公司sop執(zhí)行臨床監(jiān)查工作;

2.確保試驗嚴格按照方案、gcp及相關法律法規(guī)執(zhí)行;

3.協助研究中心解決試驗過程中可能出現的問題;

4.確保研究數據及時、準確、完整地記錄在原始病歷中，病例報告表與原始病歷數據一致;

5.及時全面地匯報研究中心進展情況;

6.完成相應書面工作;

7.協助研究者及時完成數據疑問;

8.及時、完整地收集研究相關資料;

9.完成試驗結束階段的藥品、資料整理與回收，關閉中心。

任職要求:

1. 臨床醫(yī)學、藥學等相關專業(yè)本科及本科以上學歷;有臨床風濕病工作經驗優(yōu)先;

2. 一年以上臨床監(jiān)查工作經驗;

3. 熟悉臨床試驗監(jiān)查、fda、cfda法規(guī)、ich/gcp條例;

4.與人溝通、談判、表達能力較強。

臨床協調專員崗位

第9篇 臨床學術專員崗位職責任職要求

臨床學術專員崗位職責

職責描述:

1、負責所轄區(qū)域肝病檢測項目的推廣和銷售工作;

2、根據公司銷售和開發(fā)目標，完成所轄區(qū)域的銷售和開發(fā)目標;

3、負責客戶信息的收集和上報，完成客戶業(yè)務合同的簽訂;

4、負責所轄區(qū)域內銷售活動的策劃和執(zhí)行;

5、負責所轄區(qū)域內的應收賬款的回款及上級安排的其他相關工作。

任職要求:

1、醫(yī)學或營銷類相關專業(yè);

2、從事醫(yī)療行業(yè)銷售工作1年以上，曾有過醫(yī)學檢測、肝病線藥品銷售相關經驗者優(yōu)先;

3、具備良好的溝通表達能力及團隊合作精神;

4、勤奮敬業(yè)、工作熱情主動、善于思考、執(zhí)行力強。

臨床學術專員崗位

第10篇 臨床醫(yī)學專員崗位職責要求

職位描述：

崗位職責：

1、醫(yī)學病歷撰寫、整理，影像資料的識別和分類；

2、客戶就醫(yī)完成后資料的整理和上傳，定期的隨訪跟蹤，跟蹤記錄的匯集和總結，指導進一步檢查檢驗；

3、高端客戶健康管理資料建立和方案制定；

4、負責通過檢索文獻獲得國外醫(yī)療前沿信息等；

5、公司領導安排的其他工作；

崗位要求：

1、臨床醫(yī)學或相關專業(yè)本科以上學歷，碩士以上優(yōu)先；

2、1年以上醫(yī)院臨床工作經歷優(yōu)先；

3、英語讀寫能力較好，具備專業(yè)醫(yī)學文獻的檢索、閱讀和分析能力，具有方案、文章撰寫能力者優(yōu)先；

4、工作主動，認真負責，有較強的學習能力

第11篇 臨床事務專員崗位職責

臨床事務專員 1、檢索產品臨床相關信息(包括但不限于:產品的臨床試驗情況、不良事件等);

2、負責產品說明書編寫;

3、負責臨床試驗機構篩選;

4、負責與統(tǒng)計學專家和臨床專家溝通草擬臨床方案,及臨床方案的修改;

5、負責研究者手冊和/或臨床試驗須知、知情同意書、病例報告表等相關臨床文件編寫和修改;

6、負責組織研究者(方案討論會)會議;

7、協助cra與倫理委員會和臨床試驗機構溝通;

8、協助cra進行臨床試驗啟動會準備及研究者培訓;

9、負責匯總整理臨床試驗產品使用性能反饋,并將反饋信息提交給項目經理;

10、負責統(tǒng)計報告核查,確保統(tǒng)計報告符合臨床試驗方案要求;

11、負責臨床總結報告編寫、與研究者溝通;

12、負責組織解決國家食品藥品監(jiān)督管理局醫(yī)療器械技術審評中心評審發(fā)補意見中臨床部分工作。 可接受應屆畢業(yè)生 1、檢索產品臨床相關信息(包括但不限于:產品的臨床試驗情況、不良事件等);

2、負責產品說明書編寫;

3、負責臨床試驗機構篩選;

4、負責與統(tǒng)計學專家和臨床專家溝通草擬臨床方案,及臨床方案的修改;

5、負責研究者手冊和/或臨床試驗須知、知情同意書、病例報告表等相關臨床文件編寫和修改;

6、負責組織研究者(方案討論會)會議;

7、協助cra與倫理委員會和臨床試驗機構溝通;

8、協助cra進行臨床試驗啟動會準備及研究者培訓;

9、負責匯總整理臨床試驗產品使用性能反饋,并將反饋信息提交給項目經理;

10、負責統(tǒng)計報告核查,確保統(tǒng)計報告符合臨床試驗方案要求;

11、負責臨床總結報告編寫、與研究者溝通;

12、負責組織解決國家食品藥品監(jiān)督管理局醫(yī)療器械技術審評中心評審發(fā)補意見中臨床部分工作。

第12篇 臨床研究項目專員崗位職責

臨床研究經理-項目經理-主管-專員 main tasks & responsibilities

1. contribute country specific aspects in the development of protocol, protocol revisions, amendments and crf design;

2. responsible for the management of designated sites in clinical trial including:

? site assessment;? preparation of the monitoring plan and e_ecution in compliance with visit frequency and all assigned tasks throughout the study;? planning and e_ecution of study logistics plan, including eventual delegation of activities to support group;? safety and proper conduct throughout the trial.

3. site specific data management;

4. prepare documentation for irb/ec submission/approval, together with study management per country specific requirements;

5. prepare and review clinical study agreements and budgets with study manager and contracts group;

6. ensure procedures are in place for appropriate enrollment of patients into the clinical trial;

7. organize investigator’s start-up meeting and study site initiation meetings, including training of the e_ternal study personnel in the use of the instruments and reagents and software packages for the on-line data capture and for the computer based e.g. with wincaev and training in the use of electronica crfs with remote data entry;8. responsible for instrument installation, check and validation (internal and e_ternal) for system study. if applicable, prepare workflow sheet for system studies, together with study management;

9. responsible for logistics of required evaluation/clinical trial material. informs and monitors sites for correct storage conditions;

10. preparation of all study binders;

11. perform investigator training (compliance & technical part).

12. verify the investigator follows the approved protocol and all gcp procedures;

13. verify all research staff and facilities have adequate qualifications and resources remain adequate throughout the duration of the study;

14. key contact for communications between the sponsor and the investigator; the point of first contact when investigators/site personnel enquire about patient inclusion/e_clusion criteria for ongoing trials;

15. ensure that observations during studies are correctly tracked and forwarded to the responsible departments in ____;

16. verify that source data/documents and other trial records are accurate, complete, and maintained. regarding the result calculations: ensure the usability of validated computer programs/software and result calculation in compliance to applicable sops;17. communicate deviations from the protocol, sops, gcp, and the applicable regulatory requirements to the investigator;

18. interprets and evaluates results with respect to the study goals and, if necessary, discuss with the site, the study manager, eg. interruption of the study or initiation of additional measurements at the e_ternal site;

19. perform troubleshooting for une_pected results according to study manager or protocol’s requirements;

20. ensure completion and availability of study documentation, together with study management;21. adverse events, concomitant medications, and inter current illnesses are reported in accordance with the protocol;22. conduct study close-out visits according to monitoring plan;

23. ensure ecrf and wincaev are ready for database lock;

24. archive study records / database according to guidelines;

25. responsible for post study sample/reagents/investigational use products/instruments disposition completed during the close-out visit;26. participation in project teams, global conference calls and/or meetings to review progress of ongoing clinical trials and to assess development of new projects regarding customer usability, practicability and sop development, to continuously improve quality and efficiency of the evaluation team and processes;

27. contribute to the content of the study report and contribute to publications for journals and congresses.

possible additional tasks for senior position holders;

28. responsible for investigator selection (accountability lies with study manager)

29. provide mentoring, including training on the job, to the new cras to ensure that their role and contribution is optimized.

basic requirements of the job

1. bio-medical related scientific degree; can vary from a bachelor, master and nursing qualifications;

2. knowledge of applicable standards an regulations for clinical trials and lab conduct (international conference on harmonization / who good clinical practice standards (ich-gcp), ivd directives, fda regulations)

3. practical e_perience in study monitoring according to global standards (ich)

4. 2-5 years of clinical laboratory e_perience;

5. demonstrated e_perience in computer skills to include microsoft word, e_cel, and basic templates;

6. basic statistical knowledge;

7. professional use of the english language; both written and oral;

8. open and clear communicator;

9. ability to make sound decisions and analyze and solve problems;

10. conscientious and precise delivery of work even when under pressure jd 為參考。經理-專員各級別都有。

背景優(yōu)先級:1 ivd 2 cro 3 器械 4 藥 main tasks & responsibilities

1. contribute country specific aspects in the development of protocol, protocol revisions, amendments and crf design;

2. responsible for the management of designated sites in clinical trial including:

? site assessment;? preparation of the monitoring plan and e_ecution in compliance with visit frequency and all assigned tasks throughout the study;? planning and e_ecution of study logistics plan, including eventual delegation of activities to support group;? safety and proper conduct throughout the trial.

3. site specific data management;

4. prepare documentation for irb/ec submission/approval, together with study management per country specific requirements;

5. prepare and review clinical study agreements and budgets with study manager and contracts group;

6. ensure procedures are in place for appropriate enrollment of patients into the clinical trial;

7. organize investigator’s start-up meeting and study site initiation meetings, including training of the e_ternal study personnel in the use of the instruments and reagents and software packages for the on-line data capture and for the computer based e.g. with wincaev and training in the use of electronica crfs with remote data entry;8. responsible for instrument installation, check and validation (internal and e_ternal) for system study. if applicable, prepare workflow sheet for system studies, together with study management;

9. responsible for logistics of required evaluation/clinical trial material. informs and monitors sites for correct storage conditions;

10. preparation of all study binders;

11. perform investigator training (compliance & technical part).

12. verify the investigator follows the approved protocol and all gcp procedures;

13. verify all research staff and facilities have adequate qualifications and resources remain adequate throughout the duration of the study;

14. key contact for communications between the sponsor and the investigator; the point of first contact when investigators/site personnel enquire about patient inclusion/e_clusion criteria for ongoing trials;

15. ensure that observations during studies are correctly tracked and forwarded to the responsible departments in ____;

16. verify that source data/documents and other trial records are accurate, complete, and maintained. regarding the result calculations: ensure the usability of validated computer programs/software and result calculation in compliance to applicable sops;17. communicate deviations from the protocol, sops, gcp, and the applicable regulatory requirements to the investigator;

18. interprets and evaluates results with respect to the study goals and, if necessary, discuss with the site, the study manager, eg. interruption of the study or initiation of additional measurements at the e_ternal site;

19. perform troubleshooting for une_pected results according to study manager or protocol’s requirements;

20. ensure completion and availability of study documentation, together with study management;21. adverse events, concomitant medications, and inter current illnesses are reported in accordance with the protocol;22. conduct study close-out visits according to monitoring plan;

23. ensure ecrf and wincaev are ready for database lock;

24. archive study records / database according to guidelines;

25. responsible for post study sample/reagents/investigational use products/instruments disposition completed during the close-out visit;26. participation in project teams, global conference calls and/or meetings to review progress of ongoing clinical trials and to assess development of new projects regarding customer usability, practicability and sop development, to continuously improve quality and efficiency of the evaluation team and processes;

27. contribute to the content of the study report and contribute to publications for journals and congresses.

possible additional tasks for senior position holders;

28. responsible for investigator selection (accountability lies with study manager)

29. provide mentoring, including training on the job, to the new cras to ensure that their role and contribution is optimized.

basic requirements of the job

1. bio-medical related scientific degree; can vary from a bachelor, master and nursing qualifications;

2. knowledge of applicable standards an regulations for clinical trials and lab conduct (international conference on harmonization / who good clinical practice standards (ich-gcp), ivd directives, fda regulations)

3. practical e_perience in study monitoring according to global standards (ich)

4. 2-5 years of clinical laboratory e_perience;

5. demonstrated e_perience in computer skills to include microsoft word, e_cel, and basic templates;

6. basic statistical knowledge;

7. professional use of the english language; both written and oral;

8. open and clear communicator;

9. ability to make sound decisions and analyze and solve problems;

10. conscientious and precise delivery of work even when under pressure

第13篇 臨床項目專員崗位職責

臨床項目啟動專員ssu 北京斯丹姆賽爾技術有限責任公司 北京斯丹姆賽爾技術有限責任公司,斯丹姆賽爾 崗位職責

1.根據試驗方案、合同規(guī)定的工作范圍、sop和gcp的要求進行研究中心篩選、倫理遞交、合同談判和核心文件準備等工作。

2.可同時負責多個項目、研究中心和治療領域內的研究中心啟動工作。

3.對所負責的研究中心進行方案和研究相關的溝通,為項目篩選合適的研究中心。

4.負責研究中心臨床試驗協議的談判與簽署工作。

5.負責協調研究中心啟動所需核心文件的收集、審閱、批準等工作。

6.負責研究中心倫理文件準備、遞交、溝通等工作,并協助取得倫理批件。

7.協助研究中心啟動前藥品及試驗物資的準備及分發(fā)工作。

8.通過追蹤注冊申報和批復、遞交及批準文件的溝通信、電話溝通等,管理所負責研究中心的

進展。

9.負責相應研究中心啟動階段的研究財務管理。

10.協助進行項目的可行性調研。

11.與其他職能部門共同合作。

12.完成直線經理和/或項目經理(pm)分配的其他工作。

崗位要求

1.臨床醫(yī)學、藥理學、護理學、衛(wèi)生管理或其他相關專業(yè)的大專以上學歷。

2.1年以上臨床研究、臨床監(jiān)查、臨床項目啟動或臨床協調員經驗。

3.良好的臨床研究知識,了解相關的法規(guī)要求。

4.通過公司培訓,掌握方案要求的知識。

5.良好的計算機技能,包括熟練應用微軟word、e_cel和powerpoint,以及熟練使用手提電腦。

6.良好的口頭和書面溝通能力。

第14篇 臨床數據專員職位描述與崗位職責任職要求

職位描述：

崗位職責:

1. 參與數據庫和核查程序測試

2. 按照數據核查計劃核查數據，解決數據質疑，對數據進行清理

3. 進行嚴重不良事件和外部數據的一致性核查

4. 準備數據審閱會議資料，參與數據審核會議

5. 協助項目數據經理進行數據庫鎖定

6. 數據庫及相關管理文件的歸檔

7. 完成項目數據經理分配的其余工作

任職要求：

1. 臨床醫(yī)學、護理學、藥學及相關專業(yè)專科以上學歷（接受應屆生）；

2. 良好的英語閱讀能力；

3. 工作認真、負責、細心；

4. 有良好的表達溝通能力、學習能力和接受能力；

5. 了解和遵守核心的工作流程和工作指導；

第15篇 臨床信息專員崗位職責

臨床信息專員 風和醫(yī)療器材 江蘇風和醫(yī)療器材股份有限公司,fengh medical,江蘇風和,風和醫(yī)療,風和醫(yī)療器材,風和 1、客訴信息的接受、跟蹤、了解、分析。

2、客訴問題和各部門及時溝通,在臨床角度給出產生客訴的可能

3、審查客訴診斷報告并給出到相關人員

4、必要時和客戶見面了解信息,給出客訴診斷。

5、在產品立項、研究等情況時,給出相關臨床意見

6、跟蹤新產品的動物實驗、臨床試驗,試用、使用情況,并給出意見。

7、參與質量改善,給出臨床方面意見

8、完成宣傳產品等其他相關任務。

第16篇 臨床項目專員崗位職責任職要求

臨床項目專員崗位職責

崗位職責:

1、根據時間表管理臨床項目執(zhí)行層面的各項支持工作;

2、熟練使用科技手段支持臨床試驗項目在ctms和etmf中的管理;

3、成為臨床試驗管理系統(tǒng)的使用專家并承擔管理員職責;

4、支持臨床試驗團隊進行etmf的歸檔和整理;

5、負責與公司財務進行項目相關乃至運營相關的溝通和操作;

6、支持項目經理進行供應商管理;

7、組織各類研究者會議并統(tǒng)籌會務工作。

職位要求:

1、大學本科以上，醫(yī)藥相關專業(yè)，英文讀寫流利;

2、應屆畢業(yè)生，有相關工作經驗者優(yōu)先;

3、具有計算機相關基礎知識，愿意學習新的線上程序和系統(tǒng)的應用;

4、具有基本的藥物研發(fā)知識，基本了解臨床試驗過程和對相關文件的要求;

5、 良好的溝通、表達和執(zhí)行能力，善于團隊合作，認真負責、嚴謹穩(wěn)健。

臨床項目專員崗位