1. Independently be responsible for all activities of the clinical research, including clinical site ion, study initiation visits, training of on-site personnel, study close and trial monitoring with on-site audits of clinical data for accuracy and completeness, and clinical report preparation and presentation.獨立負責(zé)臨床試驗中的所有環(huán)節(jié)，包括臨床試驗單位的選擇，臨床試驗啟動、人員培訓(xùn)、項目結(jié)題、臨床監(jiān)察，進一步負責(zé)臨床數(shù)據(jù)準(zhǔn)確性以及完整性，并且準(zhǔn)備和獲得臨床試驗報告。

2. Prepare study protocols, investigator manuals, site specific instruction manuals and design case report forms.準(zhǔn)備臨床試驗相關(guān)的所有文檔，包括臨床方案、研究者手冊、臨床單位的操作指南以及病例報告表等。

3. Assist with the management of key study parameters, including documents, clinical research products, start-up activities, enrollment, data collection, etc..協(xié)助管理臨床試驗中的所有關(guān)鍵性因素，包括文檔、臨床試驗所用產(chǎn)品、臨床試驗啟動、病例入組、數(shù)據(jù)收集等。

4. Slove the problems or issues that could affect the results or timely completion of the trial. 解決所有可能會影響到臨床試驗結(jié)果或者臨床試驗結(jié)束時間的各種問題。

任職要求：

1. 工作經(jīng)驗：Minimum of 3 years experiences with In Vitro Diagnostic (IVD), especially in molecular diagnostics or immunodiagnostics. Having the working experience in the MCN company or local well-known company is preferred. 至少3年以上體外診斷試劑領(lǐng)域臨床試驗工作經(jīng)驗,尤其是分子診斷或者免疫學(xué)診斷相關(guān)領(lǐng)域的經(jīng)驗。具有跨國企業(yè)或者本土知名企業(yè)工作經(jīng)驗者優(yōu)先。

2. 教育背景：Bachelors Degree or above of Medical/Biological related major. Master degree is prefeered. 醫(yī)學(xué)/生物學(xué)相關(guān)專業(yè)本科以上學(xué)歷，研究生學(xué)歷優(yōu)先。

3.語言技能：Fluent Reading and Writing English Communication: Highly developed interpersonal skills Characters： Well organizing details of the project, and sensitive to details. Willing to travel. 熟練的英語閱讀和寫作能力；相熟的溝通能力；良好的細節(jié)管理能力。

4.技術(shù)能力：Clinical Research Skills: Organizing clinical trial of Medical Devices/IVD, being familiar with GCP and CFDA guidelines. Multi-tasks Management: Having experience on the multi-tasks management, have the capability to handle and drive more than 3 projects at the same time.臨床試驗技巧：組織過醫(yī)療器械/體外診斷試劑臨床試驗，熟悉GCP和CFDA的技術(shù)指南；多項目管理：擁有多項目管理經(jīng)驗，并且有能力協(xié)調(diào)和開展多個項目。

EUROIMMUN was founded in September 1987 and today has its headquarters in Lübeck, Germany. In the foreground are test systems for the determination of various antibodies in patient serum in the diagnosis of autoimmune diseases, infectious diseases and allergies. The company’s reference laboratory is unequalled in the whole field of autoimmune diagnostics.
EUROIMMUN embarked China in 1999. The Beijing office has now become the headquarters of EUROIMMUN Asia Pacific. The company wins high recognition from here and has become the leader of Asian market.
歐蒙醫(yī)學(xué)實驗診斷股份公司由德國呂貝克大學(xué)Winfried St?cker博士創(chuàng)建于1987年，是世界領(lǐng)先的醫(yī)學(xué)診斷試劑及自動化儀器研發(fā)與生產(chǎn)的跨國企業(yè)。逾兩千名員工服務(wù)于全球近200個國家及地區(qū)，其產(chǎn)品和服務(wù)惠及世界五大洲數(shù)萬間實驗室。歐蒙集團在自身免疫性疾病、感染性疾病、變態(tài)反應(yīng)性疾病診斷領(lǐng)域擁有領(lǐng)先的診斷方案，在分子診斷及抗原檢測等領(lǐng)域擁有先進的技術(shù)。同時，歐蒙參考實驗室為全球用戶提供疑難樣本的診斷和驗證服務(wù)，由德國DAP認證的歐蒙全球質(zhì)量評價項目為廣大客戶提供全球?qū)嶒炇屹|(zhì)量交流平臺，助力客戶加強實驗室質(zhì)量管理。
歐蒙醫(yī)學(xué)診斷(中國)有限公司于1999年成立于北京，是歐蒙亞太集團總部。公司在中國、新加坡建立有先進的產(chǎn)品研發(fā)和生產(chǎn)基地，專業(yè)技術(shù)團隊遍及中國各省市、香港、臺灣、韓國、新加坡、泰國等國家及地區(qū)。憑借高品質(zhì)、全方位的醫(yī)學(xué)診斷方案，歐蒙的技術(shù)、產(chǎn)品與服務(wù)贏得了亞太地區(qū)客戶的高度認可與信賴，成為醫(yī)學(xué)診斷市場的領(lǐng)導(dǎo)者。