Current jobs related to Medical Affairs Clinical Operations Lead - Taipei Taipei City - Roche

  • Clinical Trials Assistant

    6 days ago

    Taipei , Taipei City, Taiwan IQVIA Full time

    Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential Functions• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...

  • Data Team Lead

    2 weeks ago

    Taipei , Taipei City, Taiwan IQVIA Full time

    Job OverviewManage end-to-end delivery of data management services for single/multi-service projects with minimal guidance, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide high quality data management products that meet...

  • 医学事务解决方案实习生Medical Affairs Solutions Intern

    5 days ago

    Taipei, Taipei City, Taiwan IQVIA Full time

    【岗位职责】支持参与医学事务解决方案(医学策略、医学教育活动、组织运营优化等)相关项目,包括:案头研究、数据收集、分析和整理一手调研资料整理&分析,包括访谈纪要整理等,并挖掘insight协助完成报告撰写,包括PPT的内容调整,版式的设计和修订,翻译等其他团队交予的...

  • Project Manager II

    1 week ago

    TWN-Taipei-Hybrid, Taiwan Syneos Health Full time

    Project Manager II / Senior Project Manager (Taiwan-based) (Pre-sourcing)Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.  Our Clinical Development model brings the...

  • Accounting Coordinator 會計助理

    5 days ago

    Taipei, Taipei City, Taiwan IQVIA Full time

    【職責】協助財務部日常作業,包括:每日付款文件整理收集並掃描各部門提交之請款文件發送付款後之通知信件,

  • Analyst/Associate Consultant, HEOR

    1 week ago

    Taipei , Taipei City, Taiwan IQVIA Full time

    Job OverviewProvides high quality, timely development and on-time input to solutions for service delivery, managed services, or implementation oriented client projects. Assignments range in complexity from basic analysis and problem solving to assisting in the development of more complex solutions to leading small teams.  Contributes to meeting client...

  • Accounting Coordinator 會計助理

    2 weeks ago

    Taipei , Taipei City, Taiwan IQVIA Full time

    【職責】協助財務部日常作業,包括:1. 每日付款文件整理2. 收集並掃描各部門提交之請款文件3. 發送付款後之通知信件, 像是提供付款證明及支票之領取4. 檔案管理5. 其他主管交付的工作【職位要求】1. 學術背景:大學畢業,不限科系,商學院優先考慮2.

  • Lead Engineer, Electrical Design

    5 days ago

    Taipei, Taiwan Celestica Full time

    Req ID: Remote Position: NoRegion: Asia Country: Taiwan State/Province: Taiwan City:  Taipei  General Overview Job Title:  Lead Engineer, Electrical DesignFunctional Area:  Engineering (ENG)Career Stream:  Design Engineering Electrical (DEE)Role:  Lead Engineer (LEN)Job Code:  LEN-ENG-DEEJob Band: 08Direct/Indirect Indicator:  Indirect Summary...

  • Medical Representative_RIV

    5 days ago

    Taipei, Taiwan AstraZeneca Full time

    職務說明透過醫院相關通路,提供處方藥品之專業諮詢服務,並執行銷售任務。維繫並持續強化客戶關係,反應客戶及市場需求,以確保達到業績目標 資歷卓越的專家客戶認可的顧問服務與合作夥伴的口碑;卓越的區域內績效目標達成與成長的表現產品趨勢與競爭對手策略分析...

  • Admin Specialist

    5 days ago

    Taipei, Taiwan IQVIA Full time

    【工作內容】辦公室日常行政庶務處理及申請行政部門款項(如物資採買、訂購與管理)合約與內部文件之建檔、掃描、維護與歸檔管理發票、傳票等財務文件之整理、建檔、核對與寄送付款、廠商資料建置之線上系統操作每週 1–2

Medical Affairs Clinical Operations Lead

3 weeks ago

Taipei Taipei City, Taiwan Roche Full time

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.The PositionRole PurposeThe Medical Affairs Clinical Operations Lead (MA COL) is a critical execution role within Medical Affairs, mainly responsible for providing operational support for affiliate-executed medical affairs programs. This role focuses on the execution, coordination, and quality oversight of RWE activities, Investigator-Initiated Studies (IIS), and Post Trial Access (PTA) ensuring all programs are conducted according to Roche quality standards, applicable regulations, timelines, and budget commitments.Core ResponsibilitiesOperational Execution forProvide day-to-day operational support for assigned Medical Affairs evidence-generation programs, with a primary focus on RWE activities and Non-Interventional Studies (NIS)Assist in the execution and tracking of study milestones from study start-up through conduct and close-outSupport the management of study documentation, including the Trial Master File (TMF/eTMF), to ensure completeness and inspection readinessBe responsible for administrative, financial tracking, and logistical tasks for assigned studies and collaborate with internal stakeholders (e.g., Medical Advisors, RWD Scientists, Finance) to ensure coordinated project deliveryFeasibility Assessment Support & Act as a SME in the teamParing with Medical Advisors, in conducting preliminary feasibility assessments for new evidence generation programs to evaluate operational opportunities, site capacity, and overall study implicationSupport the collection and analysis of country and site-level data necessary for informed operational planningBe the consultation in the Medical Affairs team to advise from the operational perspective; be the subject matter expert (SME) to guide and enhance the internal capabilities.Quality Oversight and ComplianceSupport the oversight of assigned study activities, including those managed by Contract Research Organizations (CROs) or other external vendorsAssist in monitoring compliance to study protocols, Roche Standard Operating Procedures (SOPs), and relevant regulations (e.g., ICH-GCP, GPP)Support quality control checks of clinical operations documentation and data, escalating quality issuesHelp maintain effective communication with site personnel to support high-quality study executionRequirementsQualifications:University Degree or equivalent, preferably in a medical, life sciences, or public health-related fieldExperience:Recommended > 1 years of experience in Clinical Research/Development, Clinical Operations, or a related pharmaceutical/healthcare industry setting (or equivalent academic/internship experience)Prior experience or academic exposure to clinical trial processes or medical affairs activities is a plusCompetencies:Comprehensive knowledge in clinical operations.Strong organizational skills and project management, especially exceptional attention to detailAbility to manage multiple tasks and prioritize work efficientlyEffective written and verbal communication skills in EnglishA proactive and collaborative approach to teamwork and problem-solving.Who we areA healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.Let's build a healthier future, together.Roche is an Equal Opportunity Employer.