「Senior SAS Programmer」的相似工作

1. Reads and analyzes protocol, statistical analysis plan, CRF and other trial design documents and discusses with other team members such with as biostatisticians and data managers. 2. Develops and debugs simple to complex SAS program in a timely manner 3. Implements statistical analysis plan, data preparation, and data manipulation into SAS programs and macros 4. Create analysis datasets, statistical tables, figures, and listing for clinical trial data. 5. Create CDISC standard datasets (SDTM and ADaM) 6. Participates in the validation of SAS programs and analysis datasets 7. Maintains documentation for SAS programs and validation results 8. Leads and coordinates the programming work for projects involving SAS programming if necessary 9. Coordinates timelines in orders to fulfill the needs of other departments

1. Develop and review the case report form (CRF). 2. Develop and review the database specification. 3. Develop and review the database structure on the database builder. 4. Develop and review the data validation specification. 5. Conduct the database validations including the user acceptance testing. 6. Develop and maintain the CRF library. 7. Develop and maintain the edit checks (ECS) library. 8. Develop and conduct the data review process and dummy data generation. 9. Oversee and coordinate clinical data integration activities as a DMPM. 10. Develop and update the templates of related processes. 11. Develop and manage the working process and standard operating procedures (SOPs). 12. Act as a mentor for the Associate Clinical Data Scientist I 13. Complete other tasks or assignments requested by the Supervisor.

1.依據單位需求，提供數據資料與分析報告。 2.各式專案數據分析，提供決策數據，提升團隊決策品質。 3.多維度指標體系的梳理和建設，並能完成數據資料採集、管理、分析與應用。 4.商業問題和檢視業務流程，從各種角度找到優化機會，並整合多種數據維度來佐證，提出有邏輯的分析脈絡與具體建議，進一步完成業務指標的落地。 5.其他主管交辦事項。

1. SAS programming for tables, figures and listing. 2. Protocol and synopsis design with statistical methodologies. 3. Project support / Statistical analysis. 4. Sample size estimation and power analysis. 5. Statistical analysis report/plan writing. 6. Communicate with client regarding to statistical issues.

▌Position Description: We are seeking a skilled and motivated R Programmer to join our dynamic team focused on clinical trials. The successful candidate will play a key role in the development, validation, and analysis of R codes and packages tailored for clinical trial data. This position requires a strong background in statistical programming, data manipulation, and a proactive approach to problem-solving. ▌Key Responsibilities: 1. Actively participate in the development of R codes and packages specifically designed for clinical trials. 2. Perform thorough validation of codes and analyses to ensure accuracy, reliability, and compliance with regulatory standards. 3. Independently design, develop, and debug R programs ranging from simple to complex within defined project timelines. 4. Independently implement statistical analysis, data preparation, and data manipulation using R programs and packages. 5. Independently create statistical tables, figures, and listings in R for clinical trial data, contributing to the production of high-quality reports. 6. Create and maintain comprehensive documentation for R programs, validation procedures, and results to facilitate transparency and reproducibility. 7. Collaborate with cross-functional teams, providing programming support and expertise as needed. 8. Assist in the preparation of clinical/RWE study reports, manuscripts, and other scientific documents under the guidance of senior team members. 9. Perform additional tasks as assigned, demonstrating flexibility and a proactive approach to evolving project needs. ▌Qualificaions: • Advanced knowledge of R programming • Strong understanding of biostatistical principles • Highly detail oriented, results driven • Good organizational, interpersonal, leadership and communication skills • Ability to independently manage multiple tasks and projects • Minimum BS (MS preferred) in Data Sciences, Statistics, Mathematics, Computer Sciences or related field. • 1+ years of experience in data sciences or research or drug industry using R. • Experiences in R-shiny, SAS, Python, clinical trials are plus. • Good documentation, communication and organization skills.

1. Design CRF based on study protocol and prepare the CRF completion guideline. 2. Generate data management plan and data validation plan. 3. Clinical Data Management / Clinical data management status report. 4. Provide training to the site personnel and reporting agencies on proper data collection processes. 5. Coordinate with clinical monitoring activities to help provide prompt feedback to sites on data quality. 6. Establish data quality standards and works with reporting agencies to ensure standards are met. 7. Generate and close queries or apply self evident corrections to the data according to the relevant guidelines.

ICON公司為全球前五大CRO 臨床試驗機構，全球第一大FSP公司，與全球頂尖的藥廠合作，提供專業的臨床研究服務。 提供員工良好且完整的教育訓練，透明的升遷制度，完善的休假制度，周休二日，讓員工能在良好的支援下為世界提供更新、更好的新藥品。 臨床試驗專員 1.藥品臨床試驗計畫啟動至結案過程的觀測及監督。 須具備良好的溝通能力以及敏捷的緊急應變能力，能跟試驗單位進行良好的溝通，並協助案件進行。 2.臨床試驗相關個案報告整理。須具備良好的檔案管理能力。 3.工作型態：需要出差到試驗單位(醫院)，查看臨床試驗的進度，並定期回報給專案經理，確認試驗持續符合計畫案的里程碑。出差天數依據試驗案的進程而定。 4.具備良好的英文讀寫能力，所有公司文件皆以英文撰寫。 5.目前需要具備一年以上的臨床試驗案進行經驗的人才。職級及薪水的核定將以面試來決定。面試有兩關，約在兩周內就會完成。 6. 歡迎持有身心障礙證件者投遞 Responsibilities The Clinical Research Associate is ultimately responsible for the successful management of investigator sites throughout the trial lifecycle. Key responsibilities include: 1. Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out. 2. Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan. 3. Develop effective relationships with investigator site staff to ensure that key clinical metrics are met. 4. Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies, and following up on drug safety issues. 5. Ensuring the integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines 6. Negotiation and ongoing management of clinical trial agreements with investigative sites.

工作指掌： 1. 參與產品開發流程。 2. 專案文獻收集與分析。 3. 實驗結果、數據歸納整理與分析。 4. 以口頭或書面報告形式說明實驗結果。 5. 參與臨床試驗檢體收集、臨床數據資料整理。 6. 實驗室行政庶務。 7. 主管交辦事項。 *專業職能與技術： 1. 生命科學領域相關碩士。 2. 需熟悉細胞培養技術或微生物基礎技術(分離、鑑定、活性分析等)。 3. 熟習分子生物技術(如流式細胞儀、ELISA、qPCR等)。 4. 瞭解Prism/FlowJo或其他類似軟體之技能。 5. 掌控實驗排程，並有效分配時間與資源。

【About Us】 歡迎加入「國泰健康管理」！我們是一個充滿活力、追求創新、以數據和科技驅動健康管理變革的團隊！在這裡，你將與一群熱愛科技、關心健康、充滿創造力的夥伴並肩作戰，共同探索智能健康的無限可能。 無論是伺服器系統管理師、雲端管理師，還是平台工程師，您都將在一個充滿活力的團隊中發揮關鍵作用。 您將參與設計和優化高效的系統架構，確保穩定性和安全性，並推動雲端服務的整合與創新。 您的專業知識將幫助我們提升業務靈活性，並實現可持續的增長。 【 你要做什麼呢 ？】 1.依照系統分析師（SA）開立之需求規格書，了解開發內容，並與SA討論內容，及確定開發方向及後續驗證方式。 2.以Java為開發語言，依訂立之開發規範，設計出符合需求之程式。 3.經過Code Review及單元測試完成後交付成品。 4.持續關注新技術，進行討論評估與導入應用。

1. 根據不同議題、資料來源，設計資料模型，並以視覺化報表的形式呈現分析結果 2. Data Lake / Data Warehouse 發展及數據梳理 3. 依照需求將分析結果製作成分析報告或報表 4. 主管交辦事項 ● 具備能力： 1. 擅長Excel、Word、PowerPoint 2. 熟悉SQL且會應用 3. 清晰的邏輯、良好的溝通與解決問題的能力 ● 其他條件： 1. 具備Tableau、Superset、Power BI應用經驗者尤佳 2. 具零售相關經驗者尤佳 3. 曾開發自然語言/文字探勘模型、研發數據標籤與應用者尤佳

工作內容 1. NGS數據分析與報告產出 2. 協助客製化案件分析

• 工作內容（依照職務分配）： 一、追蹤、管理計畫進度 二、資料處理分析、計畫相關事宜 三、文獻搜尋及整理 • 徵求條件： 大學以上不限科系，具公共衛生、統計及資料處理能力者尤佳。 工作經驗：不拘 語文條件：英文閱讀能力 • 公司福利：在職能力提升培訓課程，如：統計軟體使用、生物統計方法、大數據分析…等課程 • 薪資範圍：比照科技部研究計畫助理人員工作酬金支給基準表。

1.協助臨床試驗專案計畫進度追蹤，包含試驗前準備、臨床收案、受試者追蹤，及試驗資料管理等。 2. 專案計畫相關行政事務(會議記錄、供應商報帳與檔案管理等)。 3. 主管交辦事項與進行專案事項之追蹤管理。

執行試驗起始活動、試驗合約與經費協調、試驗文件與工具管理、試驗監測訪視、參與試驗各式會議、試驗進度追蹤與管理、執行試驗關閉訪視、協助試驗稽核與查核等等。

本項職缺隸屬於本院研究八所，本所主要執行能源署相關委辦研究計畫，擔任智庫幕僚，全力協助推動我國再生能源發展，達成2050淨零排放之發展政策目標。 【職務說明】 ①協助主管機關審查再生能源設置申請案件。 ②協助主管機關處理再生能源統計數據分析及檢誤，並提供參考資料。 ③協助主管機關執行委辦研究計畫、盤整產業議題，並撰寫書面報告。 ④協助舉辦、參與會議與追蹤續處進度，以及辦理其他計畫交辦事項。 【員工福利】 本院常設全院性活動(包含員工旅遊、定期聚餐及歲末尾牙等)和其他員工福利，也積極鼓勵同仁公餘籌組社團，充分聯繫、交流情誼。 此外，本所致力於營造溫暖而富有人性的工作環境，目前配有善解人意的主管、幽默風趣的同事、視主管心情補充的零食櫃；且提供持續學習空間與完整升遷制度，適性安排工作項目。 【工作時間】 週一至週五，工作時數為7.5小時(彈性上下班) ①上班彈性時間為08:30至09:30。 ②下班彈性時間為17:30至18:30。 ③固定午休時間為12:00至13:30。

1. 提供資料倉儲、功能分析處理流程、資料探勘應用的解決方案。 2. 具備清晰的邏輯能力，能快速理解使用者需求，擁有良好溝通及協調能力。 3. 負責 BI專案資料視覺化的設計與維護工作。

招募台灣地區工程師 公司提供簽證的更新以及新規簽證。 可提供高度人才簽證(5年)額外加20分，提早取得永久居留權。 執行案件為一般商業、金融案件居多，會派至委託公司駐點或在宅。 【工作內容】 1.負責軟體之分析、設計以及程式撰寫。 2.規劃執行軟體架構及模組之設計，並控管軟體設計進度。 3.進行軟體之測試與修改。 4.規劃、執行與維護量產的產品。 5.協助研發軟體新技術與新工具。 【工作職缺】Python軟體開發工程師(工作經驗三年以上) 【徵求條件】JAVA,NET,C#C,C++,Python,salesforce,SAP,PHP,IOS,Android,AWS,React.Ruby.C# （其中有一至兩項擅長的項目歡迎詢問） *無日文N1以上(可無檢定證書,但需聽說讀寫流利)請勿投遞履歷，國外遠端工作不可* 【工作地點】日本關東地區 【工作時間】9:00-18:00 中午休息1小時（依客戶現場為主） 【公司制度】1.提供雇用保險、健康保險、年金保險 2.完全週休2日、GW/夏休／年末年始連休 3.工作產生的交通費實報實銷 4.一年一度健康檢查

[Purpose of Role] The Data Processor is a member of our Project Services team, a multi-disciplinary team managing research projects from A to Z, from initial set-up to preparing client-ready deliverables. Within the team, the Data Processor are responsible for analyses and reporting. The position caters for the project deliverables and manages the project from an analytical point-of view. To do this, the Data Processor processes data(bases) in various ways, from manipulating data in analytical tools, to table reporting and charting. Together with the consultant team, the position digs into the project in search of the most important findings. The role supports senior members of the team in analysing and reporting more complex and technical challenging projects. [Responsibilities and Duties] -Responsible for the technical implementation (incl. technical 4-eye) of surveys through specialized software (e.g. Decipher) -Has a good understanding of all plug-in standard tools that are externally developed, and understand how to integrate them through standardized processes, if needed using other specialized software (e.g. MaxDiff, etc.). -Able to overcome technical difficulties if the implementation goes beyond the standard template. -Able to make basic modifications to the survey look & feel (e.g. change background, change colours & font, etc.) based on a provided design template. -Use technical skills to ensure the set-up is done in the most efficient and effective way. -Make sure that the data collection happens without any mistakes and is optimized for analysis and reporting. -Able to communicate directly with 3rd parties about technical specifications and know how to apply them in order to have them working correctly. [Technical knowledge] -Able to explain the innovations to the team when it comes to technical implications. -Basic knowledge and experience in: -Microsoft Office tools (Excel. Word, Power-Point) -Microsoft Office Outlook -Knowledge of HTML, CSS, XML -Experience with Google Survey, Suvery Monkey, Qualtrics, or any survey platform [Market Research Knowledge] -Understand the impact of applying the method correctly on actions. -Up to date with most of the common solutions Human8 is offering. [Marketing knowledge] Has a basic understanding of key marketing concepts and trends. [Project management knowledge] -Can take draft a (micro-)planning to ensure project execution as efficient and effective possible. -Understand the research goals and business impact before starting a project. -Can manage critical incidence communication. -Independent when it comes to problem solving within the domain and can link solutions between departments. [Language knowledge] Manage English at a professional level (verbal/ writing) and able to have a fluent and accurate conversation.

【About the role】 The Internal Auditor will be responsible for contributing to the design and implementation of audit processes, procedures, and methodologies, developing, and monitoring customized audit program, planning and performing operational audits to ensure compliance with applicable local and national regulations, corporate standards and generally accepted internal audit standards. 【Position Title】 (Sr.) Manager of Internal Audit 【Location】 Taipei, Taiwan. 【Reports to】 Board of Director 【Job Type】 Full-time 【Education /Background】 • Bachelor’s degree in accounting or a related field. • Qualifications for Internal Auditor required by Financial Supervisory Commission, R.O.C.(Taiwan) • More than 5 years of experience in internal auditing is required, and other related fields is a plus. • Experience in a publicly listed company (Biotech/Pharma) is preferred. • Proficient with standard concepts, procedures, protocols, and methodologies within the auditor field • Professional certification of CPA or CIA, or equivalent experience, or working towards a professional certification is required 【Responsibilities include but are not limited to】 • Establish IPO internal control policy and implement finance system. • Perform and control the full audit cycle including risk management and control management over operations’ effectiveness, financial reliability and compliance with all applicable directives and regulations • Determine internal audit scope and develop annual plans • Obtain, analyze, and evaluate accounting documentation, previous reports, data, flowcharts etc. • Prepare and present reports that reflect audit’s results and document process • Act as an objective source of independent advice to ensure validity, legality, and goal achievement • Identify loopholes and recommend risk aversion measures and cost savings • Ability to communicate independently and effectively with management, directors and departments, and to control the focus and progress of audit work • Document process and prepare audit findings memorandum • Conduct follow up audits to monitor management’s interventions 【Position Requirements & Relevant Skills & Experience】 • Advanced computer skills on MS Office, accounting software • Ability to manage large amounts of data and to compile detailed reports • High attention to detail and excellent analytical skills • Sound independent judgments and Ability to complete audit work efficiently • IPO experience is preferred

1.巡邏建築物與周遭環境，留意可疑線索，確保門窗安全。 2.回應警報器並且調查引起警鈴的原因。 3.保護被保全之人或物的安全。 4.由監視器畫面監看出入份子，以確保建築物安全。 5.給予意圖不良人士或入侵者警告，必要時報警處理。 本職位提供穩定的工作機會，有良好的晉升及發展前景。作為企業總部維安人員，你將承擔責任維護場所安全和保護內部資產，讓客戶和員工感到安全和舒適。 如果您對此職位感興趣，請提交您的簡歷和求職信，並期待與您進一步討論。