「【Global CRO Company】Clinical Data Manager」的相似工作

1. 臨床試驗的規劃與執行，包括臨床試驗流程監控、Phase 1 臨床數據分析、Phase 1/2 & Phase 2 試驗設計所需之背景資料收集與解讀。 2. 規劃並推進 長效針劑產品 BE study，包含CRO選擇、資源配置與時程管控，確保與整體 研發計畫一致。 3. 進行臨床數據與 藥理/藥代（PK/PD）分析 之審查與解讀，並撰寫醫學與科學報告，以支 持法規申請與內部決策。 4. 協助安全性監測（SAE/AE 評估、signal detection）與真實世界/背景數據分析，確保受 試者保護與醫學合規性。

- Responsible for all aspects of site management and monitoring of clinical trials - Manage interactions with all partners (investigators, site teams, internal company departments, external contractors, etc.) to facilitate successful conduct of clinical projects. - Support clinical research activities as assigned by the supervisor. - Build strong professional relationships with investigators, site staffs and internal/ external service providers. - Conduct initiation visits, monitoring visits and site closure visits in collaboration with the clinical project team. - Maintain the Trial Master File. - Prepare and negotiate site clinical trial agreements and manage clinical site budget and expenses. - Preparation of regulatory and ethics submission dossiers. - Ensure protocol-related safety reporting compliance and address and drive issue resolution. - Monitor site recruitment and establish/discuss action plans in close collaboration with the Clinical Project Manager. - Develop and conduct training for investigators and site staffs in the protocol, product and study-specific procedures. - Coordinate activities to ensure compliance with protocol, GCP, overall clinical objectives as well as company policies and SOP. - Manage trial product inventory, shipment and storage, and ensure accountability and traceability. - Ensure that imaging and/ or laboratory samples are collected, handled and shipped according to protocol requirements. - Ensure that safety reporting of adverse events is completed within required time periods. - Manage external vendor services for assigned clinical sites. - Identify issues which affect clinical trial progress and quality, and develop solutions and/ or take action to resolve/ prevent them. - Deliver projects according to expected targets, budgets and quality standards. - Monitor and report to clinical management teams on clinical trial progress, performance and plan, including subject recruitment and retention, monitoring activities, data completeness and quality, and site compliance. - Assist in the organization and conduct of internal and external stakeholder meetings, as required. - Set up, maintain and update clinical research activities and initiatives in the system.

AIBEDA is a Contract Research Organisation (CRO) specialising in medtech and AI-powered healthtech innovation. The company provides end-to-end services, including regulatory strategy, clinical protocol design, technology assessment, and market entry support, to help clients navigate the global regulatory landscape. With a focus on agility, data-driven insights, and global connectivity, AIBEDA transforms complex regulatory challenges into commercial success. Are you passionate about clinical research and project management? Are you excited about medtech breakthroughs impacting people’s health? If the answers are yes, we want to hear from you.

1. 執行臨床試驗專案計畫 (臨床試驗申請、計畫進度追蹤及管控、聯絡協調、收案結果歸檔與統計分析)。 2. 聯繫臨床試驗法規單位、臨床試驗醫院。 3. 臨床試驗案的預算規劃和成本管理 4. 協助臨床追蹤結果之期刊論文發表。 5. 市場、相關研究文獻、法規資料收集與整理。 6. 與醫院進行IRB各項行政與業務處理維護。 7. 協助制訂和維護臨床操作標準程序。 8. 其他主管交辦事宜。 請參考本公司產品及資訊 http://www.sslab.com.tw/

AIBEDA is a Contract Research Organisation (CRO) specialising in medtech and AI-powered healthtech innovation. The company provides end-to-end services, including regulatory strategy, clinical protocol design, technology assessment, and market entry support, to help clients navigate the global regulatory landscape. With a focus on agility, data-driven insights, and global connectivity, AIBEDA transforms complex regulatory challenges into commercial success. Are you passionate about clinical research? Are you excited about medtech breakthroughs impacting people’s health? If the answers are yes, we want to hear from you.

執行公司內部臨床試驗，您將作為 PMS (project management specialist)，根據專案的時程接觸到 CTA/SSU/CRA/RA相關事務 1. 管理及協調CRO、SMO、中央實驗室及研發團隊，特別針對細胞治療專案，追蹤試驗進度與技術需求，並必要時更新實驗室手冊，確保符合GTP及相關品質標準。 2. 負責臨床試驗計畫書變更之FDA及IRB送審，供應商合約簽署與費用管理。 3. 確保試驗藥品及細胞治療產品的供應與使用，必要時更新藥品手冊，並協助監控細胞治療產品的製備、運送及品質控管。 4. 追蹤試驗偏差與不良事件（AE/SAE），協助制定及執行矯正與預防措施（CAPA）。 5. 整理試驗資料與品質控管，確保數據完整並符合GCP、GTP及法規要求。 6. 與跨部門及試驗中心保持良好溝通協調，支持專案管理及問題解決，並配合細胞治療專案的特殊合規要求。

in-house協助試驗起始活動之準備、試驗合約與經費協調、試驗文件與工具管理、in-house協助試驗監測訪視相關文件準備、參與試驗各式會議、試驗進度追蹤與管理、in-house協助試驗關閉訪視之準備、協助試驗稽核與查核、in-house協助健康受試者的招募等等。

We are seeking a Clinical Operations Coordinator to oversee the planning and execution of clinical studies in compliance with GCP/ICH guidelines and company SOPs. This role serves as the primary contact for clinical trial operations and manages day-to-day activities to ensure successful study completion. 1.. Study Oversight & Compliance - Lead planning, execution, and management of clinical studies. - Ensure compliance with GCP/ICH guidelines, applicable regulations, and company SOPs. - Act as the primary point of contact for all clinical trial operational activities. 2.. Team Leadership & Coordination - Manage day-to-day activities of the clinical operations team. - Provide guidance and oversight to ensure timelines, budgets, resources, and quality standards are met. 3.. Cross-Functional Collaboration - Work closely with clinical project managers, medical monitors, pharmacokinetics, data management, regulatory affairs, and pharmacovigilance teams. - Ensure efficient and effective study conduct through cross-functional alignment. 4.. Stakeholder Communication - Communicate study progress to internal and external stakeholders. - Identify and mitigate study risks and issues proactively. 5.. Site & Vendor Management - Oversee investigational sites and third-party vendors to ensure high-quality execution. 6.. Documentation & Systems - Ensure clinical project-related documents and systems are developed and maintained to high standards.

【公司介紹】 自1970年代末，本公司配合台灣本地的醫療需求，結合國內權威的意見，添加重要電解質「磷」以及Acetate取代Lactate，開發TAITA Injection系列、PAREN AID Injection系列等適合國人的複方電解質輸液，建立臨床營養的領導地位。 PV related: ． Oversee Pharmacovigilance related activities ． PV operation: report AE/SAE cases according to Global SOP and regulation ． Conduct monthly reconciliation and literature search according to SOP ． Training management: conduct the relevant PV training ． Creation, maintenance, and HA submission of local Risk Management Plan (RMPs) and RMP report ． Aggregate Report: Manages and/or conducts oversight submission ． Perform other duties as assigned by management team

1.協助執行臨床試驗專案管理的書面作業及文書處理。 2.與試驗團隊溝通試驗操作事宜，協助解決問題，確保專案順利推進。 3.設計、準備與管理試驗相關文件，確保文件品質符合規範。 4.協助試驗報告的撰寫、遞交與通報審查單位。 5.處理試驗專案的行政庶務工作。 6.完成主管交辦的其他任務。 7.CRA工作經驗二年以上。

1. 行政與文書支援： • 協助整理與管理臨床試驗相關文件，包括會議記錄及其他行政文件。 • 管理文書檔案及資料庫，確保文件有序保存。 •準備、整理與確認臨床試驗文件（如IP文件、IRB文件等）。 •支援臨床研究團隊處理行政事務，如試驗文件寄送、資料追蹤。 2. 報帳與費用管理： • 處理試驗案費用報銷，包括差旅費、試驗相關費用等。 • 核對報帳單據的完整性和正確性。 • 與財務部門協調，確保付款流程順暢。 • 協助部門進行費用追蹤和預算報表製作。 3. 跨部門合作與溝通： • 與試驗中心及內部團隊保持良好溝通。 •協助處理主管交辦之相關任務。

**此職缺需配合11/18半天、11/19 & 11/20 & 11/21 整天** **此為Adecco派遣職缺** **也歡迎您直接將履歷郵寄至amy.chang@adecco.com ,或者直接投遞於 https://reurl.cc/0WdE3A ** 工作內容簡單好上手，為公司夥伴進行短期的櫃台代班，將負責電話接聽以及發卡接待。 Duties & Responsibility: -Receptionist -Inbound calls transfer -In/out postal/courier handling -Visitor management -Admin support (if anything urgent) Qualification & Criteria: -Experienced receptionist/admin -Quick learner who can pick-up and respond quickly for incoming call/transfer. -Pharma experience is a plus. Expected working duration: Nov. 18 13:30-17:30 orientation/handover (4 hours) Nov.19-21 8:30-12:30 /13:30-17:30 Backup receptionist (3 days)

本公司為積極前往國際市場，而擴大徵才，原設臨床研究處，擬擴大編製為三個單位，歡迎專業且富有經驗的臨床人才加入我們的團隊，共同推動多項適應症產品的臨床研究與應用，並在這過程中與公司共同成長、發展國際化的臨床及市場布局。 工作職責: 1.負責2-3個PTS潛力適應症專案之臨床資料收集及整理。 2.臨床試驗研究相關技術文件的制訂與資料分析作業。 3.準備EC、FDA送審文件(Ex: pre-IND, IND)。 4.監控進行中的臨床試驗，審閱臨床試驗報告；臨床試驗相關資訊蒐集與分析整理。 5.支持臨床項目管理活動，例如臨床試驗研究進展和醫學研究中心之可行性評估、病人招募、聯合監測、安全性資料或其它不同階段的研究活動。

• Proactively manage project level operational aspects including management of trial timeline, budget, resources, and vendors. • Provide efficient updates on trial progress to the Clinical Director and/or Senior management team, with respect to vendor selection, project plans, trial budget and timeline management, quality standards and risk mitigation. • Lead sponsor study startup process, including but not limited to conduct of the Trial Kick-off meeting, the set-up of trial master file (TMF), site selection and finalization of site and vendor Clinical Trial Agreements and budgets. • Ensure effective project plans are in place and operational for each trial and work proactively with the internal team/vendors to set priorities in accordance with applicable project plans, company standard operational procedures (SOPs), ICH/GCP guidelines and regulatory requirements. • Ensure potential study risks are escalated to the attention of the Clinical Director when appropriate. • Chair internal working group and vendor status update meetings and ensure meeting minutes are completed, distributed to team members and filed in the Trial Master File (TMF) in a timely manner. • Review and approve site visit reports; ensure tracking, follow up and resolution of site issues have been completed in a timely manner with internal team/CRO. • Monitor the quality of vendor deliverables, address quality issues with the appropriate team member and identify opportunities to improve training, execution and quality control across the clinical team. • Review and approve vendor invoices to ensure payments occur in a timely manner • Review and approve vendor responses to quality assurance audits for appropriateness, timeliness and accordance with company SOPs and regulatory requirements. • Ensure all project level study documentation is filed in the TMF in accordance with company SOPs/all regulatory requirements and provide oversight to the internal team/vendors regarding TMF filing, maintenance and archival procedure • Effectively provide support to CRO/internal team/vendors in the conduct of the trials • Support to development and review of SOPs and workflow

1. 管理與追蹤臨床受託研究機構(CRO/SMO…)公司、醫療機構之專案。 2. 管理與追蹤臨床專案執行品質、文件整理。 3. 落實臨床專案相關文件(計劃書、GCP…等)之設計、審閱與歸檔。 4. 協調臨床試驗相關事宜，加速臨床試驗進程。 5. 協助及配合臨床試驗監測與稽核。 6. 執行主管交辦其他事項。

工作內容 1.Prepare and customize the Informed Consent Form. 2.Organize translation/verification of document required for clinical trial submission. 3.Planning the clinical trial submission timeline. 4.To be responsible for preparation of TFDA/IRB submission, including the comment reply until obtaining TFDA/IRB approval. 5.To be responsible for preparation of Interim report submission and Final report submission, including the comment reply until obtaining TFDA/IRB approval. 6.Apply for IP IL permit, infectious sample export permit, NCC application for 3C device import/export. 7.Good communication with study team, manage TFDA officer and IRB staff to meet the submission timeline, and propose the resolution to the client 8. Planning the clinical contract budget and negotiate with site clinical research center to fast the CTAg execution. 9. Familiar with TFDA/IRB requirements to support the team and answer the regulatory questions from the client. ＊無經驗可，公司會進行工作技能相關訓練課程。 ＊有實際做過TFDA /IRB送審工作，且兩年以上工作經驗者優先錄取，待遇從優。

1. Prepare and Submit Regulatory Documentation: Compile, review, and submit high-quality regulatory applications, such as Investigational New Drug (IND) applications, New Drug Applications (NDA), Abbreviated New Drug Application (ANDA), and Marketing Authorization Applications (MAA), to regulatory authorities. 2. Liaise with Regulatory Authorities: Act as the primary point of contact with regulatory agencies, responding to inquiries, providing additional data, negotiating requirements, and facilitating timely approvals or resolutions. 3. Monitor and Interpret Regulatory Changes: Continuously track updates in pharmaceutical regulations, policies, and industry trends, interpreting their impact and advising internal stakeholders (e.g., R&D, legal, and marketing teams) on necessary adjustments. 4. Ensure Product Compliance: Review and approve product labeling, packaging, advertising, and promotional materials to ensure alignment with regulatory requirements, including safety, efficacy, and legal standards. 5. Manage Regulatory Submissions Timeline: Oversee the preparation and submission process to meet deadlines, ensuring all documentation is accurate, complete, and submitted in accordance with agency specifications. 6. Maintain Regulatory Records: Organize, update, and archive regulatory documentation, correspondence, and approvals in a systematic manner to support audits, inspections, and future submissions. 7. Conduct Regulatory Risk Assessments: Identify potential regulatory risks or roadblocks in product development or marketing, proposing mitigation strategies to ensure compliance and project success. 8. Handle Post-Marketing Changes: Prepare and submit regulatory applications for post-marketing changes, such as updates to manufacturing processes, labeling revisions, or formulation changes, ensuring timely approval and compliance with regulatory standards.

1.臨床試驗專案的主導、規劃、試驗進度追蹤管理、監督、回報及時程掌控。 2.管理臨床試驗相關費用與合約洽談、簽訂、付款、報帳、時程。 3.確保臨床試驗案符合GCP及相關各國法規。 4.領導跨部門團隊，協調與項目成員合作臨床試驗，案件執行管理等相關工作。 5.監督試驗過程與進度，確保所有步驟都符合GCP標準程序。 6.維護及協助臨床試驗相關文件記錄更新及管理，所有試驗文件檔案需整理並歸檔於部門內TMF。 7.其他臨床試驗相關之主管交辦事項。 8.文獻查閱及數據整理。

臨床試驗案件執行管理等相關工作 1.規劃及執行臨床試驗專案計畫. 2.協調參與試驗團隊，管控計畫進度並確保符合GCP試驗標準程序. 3.監督試驗過程與進度，並追蹤審查試驗成效. 4.專案障礙排除與危機管理. 5.合同項目執行規劃與驗收. 6.客戶關係維護. 7.監督試驗文件品質. 8.支援公司業務推廣工作.

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.