【研究方向】 1. 癌症研究：乳癌、肺癌及其他癌症之研究。 2. 微菌相研究：菌相及疾病相關性研究及生資分析。 3. 精準健康：基因體、代謝體及腸道菌之整合研究，及精準營養解決方案開發。 【工作內容】 1. 主要為撰寫研究計畫及論文。 2. 參與合作團隊會議，掌控實驗執行進度。 3. 其他主管交辦事項。 【工作地點】 輔英科技大學醫技系葉教授 實驗室 【科系條件】 1. 國內外醫學、生醫、生資及生技相關研究所之博士畢業。 2. 具細胞培養及分生相關實驗技術。 3. 具獨立撰寫研究計畫及論文能力。 【待遇福利】 1. 含勞健保年終，能力優秀者可另行調升。 2. 不定時聚餐。 3. 員工訓練。 *視能力及表現優先轉聘為編制內輔英科技大學老化及疾病預防研究中心人員。 *如具教學熱忱優先推薦轉聘為輔英科技大學專案助理教授。
*在臨床項目負責團隊的指導下執行工作。 *可與臨床試驗團隊合作制定特定研究計劃和/或流程 *進行預研究（機構資格篩選）、啟動、中期監測和結束訪問 *準備試驗機構訪問報告和確認/後續回覆 *根據試驗監測計劃與試驗機構進行定期聯繫並記錄 * 確保數據收集時間表和其成果按照在試驗機構符合試驗計劃內容。 * 與數據管理部門合作處理數據質疑工作 *依據試驗計畫和提交IRB/EC審核過的計畫內容監測試驗機構及辨識和回報試驗偏差。 *確保試驗機構遵守 SAE 報告計畫的每個協議並符合研究計劃 * 確保機構遵守研究協議並遵守臨床試驗相關法規(ICH/GCP)。為研究人員提供適當的訓練。 * 協助執行糾正措施，以解決研究中的不合規問題，包括常規訪視和品質保證審核 *追踪和報告試驗機構的進度，包括受試者篩選/註冊、數據收集、不良事件記錄和處理常見問題。 * 與內部 CRA 或指定人員合作收集、審查和追踪試驗文件，以確保試驗文件和公司中央檔案的完整性。 * 提供持續的研究相關培訓（如 EDC）並在必要時為機構研究人員提供協助 *在試驗機構管理及清點臨床試驗藥物/醫材產品，以及臨床/非臨床用品庫存，並酌情監控退貨文件。 *確保正確收集、儲存和運送實驗室樣本 *參與臨床試驗團隊會議 *協助安全管理部門收集 AE/SAE 文件以進行報告 *與試驗機構保持良好關係並快速解決任何試驗機構問題 *其他交辦事項。 *Performs job with general guidance and direction from our Clinical Project Lead, Clinical Trial Manager, or designees. *May collaborate with the Clinical Trial Manager, in-house CRA, or designee on the development of certain study-specific plans and/or processes *Conducts pre-study (site qualification), initiation, interim monitoring and closeout visits *Prepares site visit reports and confirmation/follow-up letters to sites *Conducts and documents periodic telephone contact with sites in accordance with the monitoring plan *Ensures data collection timelines and deliverables are met at assigned clinical sites in accordance with study plans *Works with Data Management in the query resolution process *Identifies and reports protocol deviations in accordance with study plans and monitors site submissions to IRB/EC per reporting policies. *Ensures site compliance to SAE reporting policy per protocol and in accordance with study plans * Ensures site adherence to study protocols and compliance with ICH/GCP/local regulations at assigned clinical sites. Provides the appropriate training / retraining to the site personnel. * Implementation of corrective actions for addressing non-compliance issues at individual sites and across study, including follow-up to routine and for-cause Quality Assurance audits *Tracks and reports progress of assigned site(s) including subject screening/enrollment, data collection, adverse event documentation, and Frequently Asked Questions * Partners with the in-house CRA or designee in the collection, review, and tracking of clinical trial documents to ensure completeness of both site files and company Central Archive * Provides ongoing study-related training (i.e. EDC) and support to site staff as necessary *Manages Drug / Medical device product and inventory of clinical / non-clinical supplies at assigned sites and monitors documentation of returns as appropriate. *Ensures proper collection, storage, and shipment of laboratory specimens * May participate in Clinical Trial Team Meetings *Assists Safety with the collection of AEs/SAEs documentation for reporting purposes *Maintains good relationships with the assigned sites and works quickly to resolve any site issues and mentoring of new employees as assigned. e.g. co-monitoring. *Perform other duties as assigned by management team.
*在臨床項目負責團隊的指導下執行工作。 *可與臨床試驗團隊合作制定特定研究計劃和/或流程 *進行預研究（機構資格篩選）、啟動、中期監測和結束訪問 *準備試驗機構訪問報告和確認/後續回覆 *根據試驗監測計劃與試驗機構進行定期聯繫並記錄 * 確保數據收集時間表和其成果按照在試驗機構符合試驗計劃內容。 * 與數據管理部門合作處理數據質疑工作 *依據試驗計畫和提交IRB/EC審核過的計畫內容監測試驗機構及辨識和回報試驗偏差。 *確保試驗機構遵守 SAE 報告計畫的每個協議並符合研究計劃 * 確保機構遵守研究協議並遵守臨床試驗相關法規(ICH/GCP)。為研究人員提供適當的訓練。 * 協助執行糾正措施，以解決研究中的不合規問題，包括常規訪視和品質保證審核 *追踪和報告試驗機構的進度，包括受試者篩選/註冊、數據收集、不良事件記錄和處理常見問題。 * 與內部 CRA 或指定人員合作收集、審查和追踪試驗文件，以確保試驗文件和公司中央檔案的完整性。 * 提供持續的研究相關培訓（如 EDC）並在必要時為機構研究人員提供協助 *在試驗機構管理及清點臨床試驗藥物/醫材產品，以及臨床/非臨床用品庫存，並酌情監控退貨文件。 *確保正確收集、儲存和運送實驗室樣本 *參與臨床試驗團隊會議 *協助安全管理部門收集 AE/SAE 文件以進行報告 *與試驗機構保持良好關係並快速解決任何試驗機構問題 *其他交辦事項。 *Performs job with general guidance and direction from our Clinical Project Lead, Clinical Trial Manager, or designees. *May collaborate with the Clinical Trial Manager, in-house CRA, or designee on the development of certain study-specific plans and/or processes *Conducts pre-study (site qualification), initiation, interim monitoring and closeout visits *Prepares site visit reports and confirmation/follow-up letters to sites *Conducts and documents periodic telephone contact with sites in accordance with the monitoring plan *Ensures data collection timelines and deliverables are met at assigned clinical sites in accordance with study plans *Works with Data Management in the query resolution process *Identifies and reports protocol deviations in accordance with study plans and monitors site submissions to IRB/EC per reporting policies. *Ensures site compliance to SAE reporting policy per protocol and in accordance with study plans * Ensures site adherence to study protocols and compliance with ICH/GCP/local regulations at assigned clinical sites. Provides the appropriate training / retraining to the site personnel. * Implementation of corrective actions for addressing non-compliance issues at individual sites and across study, including follow-up to routine and for-cause Quality Assurance audits *Tracks and reports progress of assigned site(s) including subject screening/enrollment, data collection, adverse event documentation, and Frequently Asked Questions * Partners with the in-house CRA or designee in the collection, review, and tracking of clinical trial documents to ensure completeness of both site files and company Central Archive * Provides ongoing study-related training (i.e. EDC) and support to site staff as necessary *Manages Drug / Medical device product and inventory of clinical / non-clinical supplies at assigned sites and monitors documentation of returns as appropriate. *Ensures proper collection, storage, and shipment of laboratory specimens * May participate in Clinical Trial Team Meetings *Assists Safety with the collection of AEs/SAEs documentation for reporting purposes *Maintains good relationships with the assigned sites and works quickly to resolve any site issues and mentoring of new employees as assigned. e.g. co-monitoring. *Perform other duties as assigned by management team.
1.藥品研發 2.藥品藥理文獻資料之查詢。 3.客戶藥理問題之答覆。 4.藥品GMP相關法規之查詢。 5.新產品相關資訊之查詢。 歡迎 所有求職者
呃拍謝，搜尋結果好像很少
可以嘗試調整條件、或看看你專屬的推薦工作
博士後研究員 (post-doc) 【職缺名稱】 博士後研究員1名 【徵才單位】 臺大醫院復健部治療超音波實驗室 【工作地址】 臺大醫院復健部 【工作內容】 動物實驗 【徵才條件】 國內外博士 【薪資待遇】 依國科會規定 【聯絡方式】 請將履歷表、自傳(含相片)、發表論文及相關學經歷 寄至[email protected] , 若詢問實驗相關內容請洽 02-23123456#67747 廖先生 【其他備註】 1.信件標題請註明 應徵「博士後研究員」 2.適合者通知面試，不適者不另通知
1.負責各部門及外部合作單位溝通聯繫，整理外部回饋資訊予公司內部單位。 2.負責專案管理(協助專案規劃、實施及管控專案進度與追蹤檢討、產品檔案維護等)。 3.負責研發計畫/論文/QMS/ISO/DHF/文件撰寫、維護及更新。 4.負責研發實驗，試驗數據彙整分析、實驗紀錄或報告撰寫。 5.負責各項補助及臨床計畫申請、管理與執行。 6.其他主管交辦事項。
一、工作內容 1.基因研究：我們擁有來自於英國、台灣等地的基因資料庫，並且還包括特定疾病如CKD與乳癌等的基因資料庫 2.衛生政策研究：我們涉及國際衛生、兒童醫療照護、成人預防保健等議題，致力於制定更具前瞻性與有效性的政策方案 3.行為研究：我們關注健康行為、多重行為、內外化行為及運動行為等，旨在探索人類行為背後的科學與意義 如果您對於跨領域研究充滿熱情，並且渴望在國際化的環境中發展您的學術生涯，歡迎加入我們的團隊 投履歷時，請註明您應聘的職缺以及您的專業領域，不限於單個 Interdisciplinary Integration, Pioneering the Future We stand apart from traditional research teams as our expertise spans across various domains including genetics, behavior, and health policy. Committed to fostering innovation and advancement, we operate within a collaborative framework engaging with industry, communities, government, and academia. Job Openings: Postdoctoral Research Fellow Research Assistant (Master's level) Research Assistant (Bachelor's level) Job Responsibilities: Genetics Research: Leveraging genetic databases from regions like the UK, Taiwan, and specialized repositories focusing on specific conditions such as CKD and breast cancer. Health Policy Analysis: Addressing international health, pediatric healthcare, adult preventive care, and other pertinent topics to formulate proactive and impactful policy interventions. Behavioral Studies: Investigating health behaviors, multiple behaviors, internalizing and externalizing behaviors, and exercise behaviors to understand the scientific underpinnings and implications of human behavior. If you are passionate about interdisciplinary research and eager to develop your academic career in an international environment, we welcome you to join our team. When submitting your application, please specify the position(s) you are applying for along with your area(s) of expertise, but not limited to a single one. 二、工作技能 1.具有基因、公衛、運動醫學、物理治療、醫護、醫管、大數據與統計等相關背景佳，但不限於上述科系 2.主動積極、學習能力強、認真負責、細心耐心、有責任感者 3.良好理解能力、文獻蒐集、報告彙整及撰寫能力。 4.具良好的資料整理、統計分析能力，熟悉SAS、SPSS、STATA或R等統計軟體尤佳 5.熟悉電腦、文書處理軟體(如Office Word、Excel、Power Point等) 6.具健保資料庫分析、資料探勘與數據分析、機器學習等能力者優先錄取 三、薪資金額 以｢衛生福利部及所屬機關研究計畫助理人員約用注意事項｣辦理給付標準為參考依據，試用期後視工作能力調整！
1、微生物培養與醱酵。 2、醱酵產物分析。 3、培養真菌、細菌、乳酸菌等微生物，觀察其生態環境、量產環境下的特性與表現行為，藉此增加學理上的了解，並發展臨床上的食療用途。 4、細心並能主動學習者，並且具良好溝通協調能力，能夠配合團隊工作者，具撰寫研究計劃能力為佳。
The Tsai lab at the University of Virginia School of Medicine is seeking to hire 1-2 Research Assistants to assist in the study of ion-channel structure, molecular mechanisms, and pathophysiological functions. We are currently investigating the molecular mechanisms and pathophysiological roles of the mitochondrial calcium transport system, whose malfunction has been linked to the Alzheimer's disease, tissue injuries during heart attack and stroke, cancer metastasis, and type II diabetes. We combine cutting-edge electrophysiology, membrane-biochemistry, cell-biology, imaging, animal models, and structural-biology (e.g., cryo-EM) methods to address fundamental questions in this exciting new area of research. For more information, please visit our lab website: www.tsaislab.org We seek to hire a master's level researcher interested in becoming a future scientist. Our goal is to identify new lab members to work with us to push the frontier of science. Once accepted into the lab, the RA will be assigned his/her own project with a difficulty level consistent with typical PhD dissertation projects, and will initially work with senior lab personnel to acquire necessary techniques for assigned projects. All RAs in the Tsai lab work closely with the PI, and have a strong record of publishing in high impact journals. They will have the opportunities to become PhD students in the Tsai lab, with results obtained during the RA period counting toward graduation. The lab is currently supported by two NIH R01s, and have plenty of funding in the next 5 years. Senior-author research papers in the last 5 years were published in eLife, PNAS (2 articles), Cell Reports, Nature, and Molecular Cell. There are additional articles in the late stage of the review process in Nature and Nature Structural & Molecular Biology. We have extensive collaboration with scientists in Cornell, Harvard, Washington University at St. Louis, Sloan-Kettering, Mount Sinai, University of Michigan - Ann Arbor, and Stanford. The University of Virginia ranked #5 in US public Universities (only after UC Berkeley, UCLA, U Michigan, and UNC) according to the 2023 US News ranking. Charlottesville is a vibrant and expanding city, only 2 hours of driving away from the US capital Washington DC, with easy access to a wide range of cultural and outdoor activities. Applicants should send a cover letter, CV, and a list of three references directly to the PI ([email protected]). The letter should clearly outline the candidate’s qualifications and the motivation to join our lab.
1. 進行細胞量產程序開發，提高生產效率，包括3D系統和高密度培養 2. 建立不朽化細胞株，包括特性分析和長期生長能力鑑定 3. 培養基組成優化 4. 細胞培養肉和保健品認證申請 5. 其他主管交辦事項