更新于 12月24日

CRM/臨床監(jiān)查經(jīng)理(CRA-LM)

2.5-3.5萬
  • 廣州越秀區(qū)
  • 5-10年
  • 本科
  • 全職
  • 招1人

職位描述

藥品臨床研究CRA新藥仿制藥化學(xué)藥生物藥Ⅰ期Ⅱ期Ⅲ期
職責(zé)描述:
1.Manage staff in accordance with organization’s policies and applicable regulations, Responsibilities include planning, assigning, and directing work, appraising performance and guiding professional development; rewarding and discipline employees; address employee relation issues and resolving problems. Approve actions on human resource matters.
根據(jù)組織政策和適用法規(guī)管理員工,職責(zé)包括計(jì)劃、分配和指導(dǎo)工作,評(píng)估員工績效及指導(dǎo)其專業(yè)發(fā)展;獎(jiǎng)勵(lì)和懲戒員工;員工關(guān)系的處理及問題的解決。完成員工人力資源事務(wù)的審批。
2.Participate in the selection and onboarding process for new CRAs by conducting candidate review and participating in the interview process. Conduct onboarding training for new staff in conjunction with Human Resource and learning and Developing training programs.
通過對(duì)候選人的審查并參加面試過程,參與CRA的招聘和入職流程,結(jié)合人力資源制定培訓(xùn)計(jì)劃,對(duì)新員工進(jìn)行入職培訓(xùn)。
3.Ensure that staff has the proper materials, system, access and training to complete job responsibilities. Provide oversight for the execution of the training plan and SOP review.
確保員工有適合的資料、系統(tǒng)、權(quán)限和培訓(xùn)來完成工作職責(zé)。對(duì)培訓(xùn)計(jì)劃和SOP閱讀的執(zhí)行進(jìn)行監(jiān)督。
4.Participate in allocation of resources to clinical research projects by assigning staff that are appropriate to their experience and training.
委派經(jīng)驗(yàn)豐富和已完成培訓(xùn)的員工參與臨床研究項(xiàng)目,分配項(xiàng)目資源。
5.Manage the quality of assigned staff’s clinical work through regular review and evaluation of the work product.
通過對(duì)工作成果的定期回顧和評(píng)估,監(jiān)管員工的工作質(zhì)量。
6.Ensure operational processes, systems and standards are adopted and implemented consistently across trials.
確保在整個(gè)試驗(yàn)中采用一致的操作流程、操作系統(tǒng)和實(shí)施標(biāo)準(zhǔn)。
7.Identify quality risks and issues and create appropriate corrective action plans to prevent or correct deficiencies in performance of staff. Drives team members to improve their efficiency and effectiveness at prioritizing work and improving performance.
識(shí)別質(zhì)量風(fēng)險(xiǎn)和問題,并制定適當(dāng)?shù)募m正措施計(jì)劃,以避免或糾正員工在績效方面的不足。推動(dòng)團(tuán)隊(duì)成員提高工作效率和有效性,安排工作優(yōu)先級(jí),提高績效。
8.Drive plans to resolve Clinical Operations issues escalated from team members. Drive team initiatives and develops solutions independently.
就團(tuán)隊(duì)成員提出的臨床操作問題提出解決計(jì)劃。能獨(dú)立提出解決方案以推動(dòng)團(tuán)隊(duì)的積極性。
任職要求:
1.A Bachelor (or above) degree in life sciences, pharmacy nursing or medical, at least 5 years’ experience in clinical trials.
本科及以上學(xué)歷,生命科學(xué)、藥學(xué)、護(hù)理或醫(yī)學(xué)相關(guān)專業(yè),5年以上臨床試驗(yàn)行業(yè)經(jīng)驗(yàn)。
2.Good knowledge of Clinical Operations processes and systems.
良好的臨床運(yùn)營流程及系統(tǒng)相關(guān)知識(shí)。
3.At least 1-year CRA management experiences in the position of CRM or Project management.
至少一年人員管理或項(xiàng)目管理崗位的CRA管理經(jīng)驗(yàn)。
4.Demonstrate effective coaching/leadership/supervisory ability including excellent interpersonal skills.
具有優(yōu)秀的輔導(dǎo)/領(lǐng)導(dǎo)/管理能力,以及出色的人際交往能力。
5.Good planning,organization and presentation skills.
良好的計(jì)劃、組織能力與演講能力。
6.Effective time management skills and ability to manage competing priorities.
高效的時(shí)間管理能力,能夠管理沖突的優(yōu)先級(jí)。

工作地點(diǎn)

白云大廈501C

職位發(fā)布者

王麗華/HR

昨日活躍
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昆翎(ClinChoice)是一家致力于為生物醫(yī)藥和醫(yī)療器械客戶提供高品質(zhì)一站式服務(wù)的臨床階段CRO,服務(wù)包括臨床運(yùn)營、項(xiàng)目管理、生物統(tǒng)計(jì)、數(shù)據(jù)管理、注冊(cè)事務(wù)、醫(yī)學(xué)事務(wù)和藥物警戒。昆翎已經(jīng)在中國、美國、歐洲、印度、日本和菲律賓建立了主要的臨床交付中心,目前在全球擁有1800多名員工,其臨床運(yùn)營團(tuán)隊(duì)覆蓋了亞、歐、北美等七個(gè)國家和地區(qū)。高盛直投部董事總經(jīng)理、昆翎董事會(huì)成員許小鷗先生認(rèn)為,“隨著創(chuàng)新療法在全球的增長,CRO公司提供高效、可靠的研發(fā)服務(wù)能力變得尤其重要。昆翎獨(dú)特的價(jià)值主張結(jié)合了其對(duì)于本地市場的了解、國際藥物研發(fā)的經(jīng)驗(yàn)以及高效的團(tuán)隊(duì)執(zhí)行能力。我們堅(jiān)信公司強(qiáng)勁的管理層團(tuán)隊(duì)以及其高效的執(zhí)行能力,將為昆翎的發(fā)展開啟新的篇章。
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