崗位職責(zé):
1、協(xié)助項(xiàng)目經(jīng)理完成試驗(yàn)核心文件的收集、整理、核查和歸檔;Assist the project manager in collecting, organizing, checking, and archiving the core documents of the trial.
2、協(xié)助項(xiàng)目經(jīng)理收集試驗(yàn)相關(guān)信息,負(fù)責(zé)對(duì)臨床試驗(yàn)進(jìn)度做整體跟進(jìn)、匯總及匯報(bào);Assist the project manager in collecting relevant information for the trial, and be responsible for the overall follow-up, summarization, and reporting of the clinical trial progress.
3、跟進(jìn)項(xiàng)目監(jiān)查計(jì)劃、重點(diǎn)問題處理的執(zhí)行情況;Follow up on the implementation of the project monitoring plan and the handling of key issues.
4、協(xié)助項(xiàng)目組召集、組織網(wǎng)絡(luò)及電話會(huì)議,組織、籌備、協(xié)調(diào)項(xiàng)目現(xiàn)場會(huì)議;Assist the project team in convening and organizing online and telephone meetings, and organize, prepare for, and coordinate on-site project meetings.
5、負(fù)責(zé)處理項(xiàng)目組其他行政工作;Be responsible for handling other administrative tasks of the project team.
6、完成上級(jí)經(jīng)理分配的其他工作。Complete other tasks assigned by the supervisor.
任職要求:
1.本科及以上學(xué)歷,臨床醫(yī)學(xué)、預(yù)防醫(yī)學(xué)、臨床藥學(xué)等臨床相關(guān)專業(yè)優(yōu)先;Bachelor
s degree or above, with priority given to clinical-related majors such as clinical medicine, preventive medicine, and clinical pharmacy
2.熟悉藥物臨床試驗(yàn)管理規(guī)范(GCP)和臨床工作相關(guān)法規(guī),了解臨床研究實(shí)施流程;Be familiar with the Good Clinical Practice (GCP) and relevant regulations for clinical work, and understand the implementation process of clinical research.
3.有良好的工作態(tài)度,工作嚴(yán)謹(jǐn),有責(zé)任心,協(xié)調(diào)溝通能力強(qiáng),有良好的團(tuán)隊(duì)精神與合作意識(shí);Have a good work attitude, be rigorous in work, responsible, with strong coordination and communication skills, and possess good team spirit and cooperative awareness.
4.熟練應(yīng)用電腦及辦公軟件;Proficient in computer operation and office software