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5/02 2567 Medical Science Liaison

  • 台北市中山區
  • 2年以上
  • 碩士

OUR COMPANY At Boehringer Ingelheim we develop breakthrough therapies that improve the lives of both humans and animals. Founded in 1885 and family-owned ever since, Boehringer Ingelheim takes a long-term perspective. Now, we are powered by 52,000 employees globally who nurture a diverse, collaborative and inclusive culture. We believe that if we have talented and ambitious people who are passionate about innovation, there is no limit to what we can achieve. THE POSITION Focusing on scientific communication on heart failure, chronic renal disease and diabetes (Cardio-Renal-Metabolism) for BI -related products & new indications. To provide scientific information to SEs/HCPs(scientific expert/ healthcare professionals ), to implement medical programs, and support medical/scientific needs of SEs/HCPs in assigned therapeutic area. To provide scientific information to SEs/HCPs(scientific expert/ healthcare professionals ), to implement medical programs, and support medical/scientific needs of SEs/HCPs in assigned therapeutic area. Tasks & Responsibilities - Effective and scientific communication with SEs to provide the most wanted and up-to-date scientific information of BI products and related therapeutic area including response to external enquiries through credible and clear non-promotional way - Develop and implement KOL management plan, and build up scientific network with KOL - Provide scientific support to medical/marketing activities by facilitating scientific presentations and medical education programs - Execute the plan of data dissemination & publication and works with key scientific experts - Implement medical plan and activities, e.g, advisory board meeting and CME/SEM(continue medical education/scientific expert meeting) - Deliver up-to-date BI products and related therapeutic area information to marketing and sales force and provide training in a regular basis - Coordinate all local clinical trials programs (e.g., Phase IV studies, IIS(investigator initiated studies), NIS(non-investigate study), PMS(post marketing surveillance), registry, CUP (Compassionate Use program)etc. - Identifies opportunities to improve methodology and provide practical solutions to Medical Affairs, and may work with a team to implement these improvements and solutions. Requirements - Master in health science, PharmD, PhD, MD - Minimum 2 years working experience of pharma industry - Good knowledge of clinical study methodology, study design, data review and analysis, publication processes - Summarize the medical information and conduct medical input - Highly medical project management skills to deliver on complex tasks within timeframe and milestones - Good communication skills both in English and Chinese; Ability to communicate clinical and non-clinical technical information effectively - Good presentation skills - Project management ability WHY BOEHRINGER INGELHEIM? With us, you can grow, collaborate, innovate and improve lives. We offer challenging work in a respectful and friendly global working environment surrounded by a world of innovation driven mindsets and practices. In addition, learning and development for all employees is key, because your growth is our growth. Want to learn more? Visit www.boehringer-ingelheim.com READY TO CONTACT US? Please contact our Recruiting Team: Name, TW: +886-225129622; [email protected] POSITION AREA Medical POSITION LOCATION Taiwan , Taipei ORGANIZATION TW – Boehringer Ingelheim Taiwan Ltd SCHEDULE Full time

待遇面議 外商公司 員工300人 距捷運行天宮站約500公尺
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0~5人應徵

5/02 R&D Senior Scientist I / II for pharmacology_PKPD

  • 台北市南港區
  • 2年以上
  • 碩士

• Represent clinical pharmacology for the assigned study team to support clinical study conduct from clinical pharmacology perspectives. • Translate nonclinical data to human efficacious dose projection. • Design experimental PK or PKPD studies in animal or human to better understand the clinical pharmacology of compound in development. • Conduct Non-Compartmental Analysis (NCA) for nonclinical and clinical PK studies and writing the PK reports. • Work with vendor or perform in-house population PK and PKPD analyses. • Responsible for preparation of regulatory submissions such as IND submission, and response to health authority’s questions with respect to clinical pharmacology.

月薪47,000元以上 員工135人 距捷運南港站約270公尺
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0~5人應徵

5/02 臨床試驗案專員

  • 台北市中正區
  • 2年以上
  • 大學

1. 管理並支援臨床試驗中心的臨床護理師收案相關事宜，協助費用報支申請。 2. 控管臨床試驗中心藥品與經費狀況，維持案件持續執行。 3. 控管委外檢驗報告的進度，匯總檢驗數據，申請費用報支。 4. 管理官方文書，匯整更新臨床試驗相關文件。 5. 了解各國臨床法規，並執行公司後續產品臨床收案計畫。 6. 產品臨床法規、標準之蒐集/彙整更新及維護。

月薪36,000~42,000元 員工30人 距捷運台大醫院站約250公尺
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0~5人應徵

5/02 技術專員(技術組)

  • 新北市汐止區
  • 1年以上
  • 大學

1、GLP動物試驗：一般毒性試驗、毒理動力學、安全藥理學、生殖毒理等操作經驗。 2、GLP試驗數據計算及紀錄文件整理。 3、實驗室儀器設備操作與維護。 4、主管交辦事項。 5、須配合例假日值班。

待遇面議 上市上櫃 員工130人
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0~5人應徵

5/02 Medical Science Liaison

  • 台北市內湖區
  • 2年以上
  • 碩士

1. Conduct presentations to clinicians, academia and other potential collaborators about the scientific principles and clinical applications of ACT Genomics’tests 2. KOL identification, prioritization and engagement 3. Identify and provide unbiased medical and scientific information to clinicians 4. Collect insights from the field, feedback to internal stakeholders and implement them into company’s medical affairs strategies 5. Conduct ongoing training for distribution partners, customers, and corporate colleagues including TW, HK, and SEA. 6. Understanding, comprehension and compliance to genetic testing guidelines in the region 7. Collaborate with the marketing and sales teams to develop and update supporting materials. 8. Address inquiries and requests related to clinical applications, leveraging in-depth knowledge of clinical data from conference, publications, and clinical trials. 9. Support organizing scientific and educational events 10. Able to travel 30-50% of time 11. The position may require the flexibility to work on evenings and weekends (field activities)

待遇面議 員工200人
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6~10人應徵

5/02 臨床研究資深專員 Senior Clinical Research Specialist

  • 新北市土城區
  • 5年以上
  • 碩士

在Wellell，身為臨床研究員，您將負責協助公司執行產品臨床評估、臨床試驗、上市後追蹤…等研究計劃，並確保產品遵循醫療法規要求與標準，達到臨床效益並符合公司期待 [工作內容] 1.撰寫公司產品的臨床評估計劃及報告 2.設計臨床試驗計劃，申請IRB臨床許可，與醫院合作執行臨床試驗，完成研究報告的撰寫 3.規劃及執行上市後臨床追蹤活動 4.協同品牌行銷部門規劃及執行臨床行銷活動(如：醫學年會發表) 5.建立及經營醫療院所之專家顧問的關係，並與其合作評估產品的臨床性能 或執行臨床試驗 6.內部分享及教育訓練相關臨床知識 7.定期執行臨床文獻探索，找尋特定適應症相關未滿足需求

待遇面議 上市上櫃 員工650人
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0~5人應徵

5/01 In House CRA (Core Team)

  • 台北市信義區
  • 經歷不拘
  • 大學

In House CRA ICONs Clinical Operations team is actively looking to hire a significant number of In-house CRAs. You will be part of our world class development program which fast tracks your growth into a traveling CRA. If you enjoy travel, are ready for your next step in your clinical research career, and are passionate about ICONs mission to bring life-saving therapies to market, this is your chance to join the team! ICON's award-winning study execution capabilities have led to the approval of 18 of the world's top 20 best-selling drugs. As a global provider of drug development solutions, our work is serious business. But that doesn’t mean you can’t have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry. Are you one of them? Apply Now. The role: • Become familiar with ICON’s SOPs/WPs, ICH GCP guidelines, appropriate regulations, ICON systems and the principles of and assist with investigator recruitment • Maintain timelines and ensure accuracy and completeness of data entered into ICON systems • Serve as the primary in-house contact for sites and investigators participating in studies • Conduct and completes remote site management activities, with support as needed, according to applicable SOPS and the Study Monitoring Plan. • To contact Clinical sites for specific requests (e.g. enrolment updates, missing documentation, data entry timeliness, data query follow-up, CDA finding follow-up, and action Item resolution or other sponsor specific CRA tasks. • Take responsibility for project tasks and sees these tasks through to successful completion, with support. • Maintain a professional interpersonal relationship with study team, sites, and Sponsors • Participate in QA Audits as needed. • Regularly attend and gives to project specific and departmental meetings • Ability and willingness to travel as needed (drive and fly) • Maintain Sponsor and patient confidentiality • Other duties as assigned You will need: • Minimum Bachelor's degree in a life science • At least 12 months of a CTA/Clinical Trial Assistant or similar role experience within the clinical/pharmaceutical industry • Understanding of ICH GCP Compliance • Excellent communication and organizational skills • A phenomenal teammate

月薪50,000~70,000元 外商公司 員工300人 距捷運台北101/世貿站約300公尺
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11~30人應徵

4/30 Clinical Tech Supporter I

  • 台北市中山區
  • 經歷不拘
  • 大學

▌Position Description: The Clinical Tech Supporter I is a specialized role in the field of clinical research. This role is responsible for providing technical support and expertise for electronic data capture (EDC) systems and related applications utilized in clinical research studies. The Applications Support Engineer plays a crucial role in ensuring the efficient functioning of EDC systems and the accurate collection and management of clinical trial data. ▌Key Responsibilities: 1. Collaboration with Study Teams: ▪ Work closely with study teams, including clinical investigators, project managers, and statisticians, to gain a deep understanding of data collection requirements and study protocols. ▪ Collaborate with stakeholders to define data standards and ensure alignment with study objectives. 2. Design and Configure eCRFs: ▪ Utilize expertise in data management and EDC systems to design and configure electronic case report forms (eCRFs). ▪ Ensure that eCRFs are tailored to specific study requirements, capturing all essential data points necessary for analysis. ▪ Collaborate with study teams to customize eCRFs according to study protocols and objectives. 3. User-Friendly eCRFs: ▪ Pay special attention to user-friendliness when designing eCRFs to facilitate ease of use for clinical site personnel and data entry personnel. ▪ Implement user-friendly features such as clear instructions, data validation checks, and logical data entry flows. ▪ Continuously gather feedback from end-users to improve eCRF design and usability. 4. Utilize Programming Languages and EDC-Specific Tools: ▪ Proficiently use programming languages such as SQL, SAS, R, and EDC-specific tools to develop custom functionalities and edit checks. ▪ Implement these custom functionalities to ensure data accuracy, consistency, and compliance with data standards. 5. Testing and Issue Resolution: ▪ Conduct thorough testing of eCRFs, edit checks, and data capture processes to identify and promptly resolve any issues or discrepancies. ▪ Collaborate with the study team to ensure the reliability and integrity of collected data. 6. Data Collection and Entry: ▪ Develop data collection tools and electronic data capture (EDC) systems. ▪ Oversee and ensure the accurate and timely entry of clinical trial data. ▪ Monitor data collection processes to identify and address discrepancies and issues. 7. Data Validation and Cleaning: ▪ Implement data validation checks and edit checks to identify errors and inconsistencies in collected data. ▪ Collaborate with clinical site personnel to resolve data queries and discrepancies. ▪ Maintain data integrity and quality throughout the trial. ▌Qualificaions: ▪ Bachelor’s degree in biological science or a related field. ▪ Ability to plan, multitask and work in a dynamic team environment. ▪ Strong verbal and written communication skills. ▪ Excellent computer skills, including proficiency in MS Office (Word, Excel, PowerPoint, Office, Project). ▪ Ability to manage and prioritize workload effectively.

待遇面議 距捷運行天宮站約90公尺
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0~5人應徵

4/30 (醫學)學術編輯

  • 台北市大安區
  • 經歷不拘
  • 碩士

【工作內容】 1. Medical Writing： 撰寫醫學研究相關文件或製作物，包括醫學會議紀錄、醫學簡報、診治指引、論文編修等 2. Medical Editing： 提供指引予外部合作編輯，確認外部編輯完成稿件品質(含醫學文件的編輯和校對)，包括作品的呈現方式、內容的正確性、表達的一致性等 3. Medical Communication： 與客戶溝通醫學文件或製作物內容，理解客戶需求並適時提供建議，協助客戶完成相關學術活動(如期刊投稿、共識會議等) 4. Others： 出席會議 【其他需求】 1. 履歷能檢附醫藥相關文字作品尤佳 2. 具備論文編修、期刊投稿經驗 3. 樂意與團隊分享經驗，一同規劃提升醫學編輯技巧的方式 我們可以提供給您： ※彈性之出勤制度 ※加班誤餐費補貼 ※穩定調整的薪資待遇 ※舒適、輕鬆的工作環境，充足的咖啡(研磨及膠囊)、飲料、零食、泡麵 ※寵物友善的空間，歡迎家中寵物來玩

年薪800,000~1,200,000元 距捷運國父紀念館站約270公尺
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0~5人應徵

4/30 醫學編輯(Medical Writer)

  • 台北市大安區
  • 經歷不拘
  • 大學

【工作內容】 1. Medical Writing： 撰寫醫藥行銷、病人衛教、醫學研究相關文件或製作物，包括醫學會議紀錄、醫學簡報、醫藥行銷文案、衛教資訊、診治指引等 2. Medical Editing： 醫學文件／製作物的編輯和校對，包括作品的呈現方式、內容的正確性、表達的一致性等 3. Medical Communication： 對外與客戶溝通醫學文件或製作物內容，理解客戶需求並適時提供建議；對內與設計部門合作，討論醫學製作物的最佳呈現方式 4. Others： 出席醫學會議 【其他需求】 1. 履歷能檢附醫藥相關文字作品尤佳 2. 中文文筆精準、柔順 3. 樂意與團隊一同鑽研提升醫學編輯技巧 我們可以提供給您： ※彈性之出勤制度 ※加班誤餐費補貼 ※穩定調整的薪資待遇 ※舒適、輕鬆的工作環境，充足的咖啡(研磨及膠囊)、飲料、零食、泡麵 ※寵物友善的空間，歡迎家中寵物來玩

年薪750,000~1,000,000元 距捷運國父紀念館站約270公尺
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11~30人應徵

4/30 Clinical Project Specialist (臨床專案專員)

  • 台北市信義區
  • 1年以上
  • 大學

General Statement: Provide the overall supports for the implementation and conduct of clinical trials in accordance with prevailing laws and ICH GCP within established timelines and budgets Reports to: Chief Operating Officer Primary Duties and Responsibilities, including mental requirements of position: 1. Work closely with Clinical Project Manager 2. Understand clinical trial protocol and support the communications with clinical sites and vendors on the study conduct 3. Support study budget planning and communicate with the internal stakeholders 4. Manage the contract, purchase order process, and process the invoices of investigator sites and vendors 5. Update and maintain project tracking systems and schedules 6. Coordinate import and export for clinical trial materials 7. Manage and maintain clinical trial related documents 8. Coordinate meetings, prepare meeting slides and meeting minutes

月薪40,000元以上
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11~30人應徵

4/30 研究專員(TRC)

  • 台北市南港區
  • 經歷不拘
  • 碩士

1. 進行藥物篩選、功能驗證 2. 進行新技術之開發 3. 耗材請購 4. 負責儀器之維護管理，含維修連繫、使用規範建立及執行教育訓練 5. 執行其他公司或部門指派任務

待遇面議 員工180人
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6~10人應徵

4/30 助理研究員/副研究員(藥理研究)

  • 台北市南港區
  • 經歷不拘
  • 碩士

1. 操作細胞與動物實驗以評估藥效(熟悉動物試驗相關技術尤佳，如靜脈注射、採血、大小鼠操作…)。 2. 抗體藥物複合體新藥研發(熟悉蛋白質純化技術尤佳)。 3. 分生技術操作(熟悉SDS-PAGE、Western blot、ELISA等技術)。 4. 實驗方法開發與設計。 5. 試驗相關數據紀錄、整理與系統分析。 6. 文獻與研究資料蒐集與整理。 7. 主管交辦事項。

待遇面議
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0~5人應徵

4/30 RD2-1 副研究員/研究員(新藥開發)

  • 新北市汐止區
  • 經歷不拘
  • 碩士

如果您對次世代抗體藥物有高度興趣且熟悉抗體、追求卓越勇於挑戰，我們期待您的加入，一起為癌症新藥開創不一樣的未來! (1) 設計與優化抗體藥物序列(Next-generation mAb) (2) Molecular cloning實驗設計與操作 (3) 抗體結構模擬與分析 (4) Basic molecular biology/cell biology assays，如ELISA, Western blot, Flow cytometry等。 (5) 研發專案管理 (6) 其他主管交辦事項

待遇面議 員工50人
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6~10人應徵

4/30 Cell Associate Scientist (細胞副研究員)

  • 新北市五股區
  • 經歷不拘
  • 碩士

1. Cell culture 2. Membrane-based and Cell-based functional assays 3. Radio-labeled assays and animal tissue extraction 4. New project or assay development, data analysis, literature review and search 5. Assay troubleshooting, optimization and validation 6. Equipment maintenance and SOP document system management 7. Brainstorming for innovative ideas on new assay method or new testing platform setup 8. Team support and other task assigned by supervisor

待遇面議 員工130人
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0~5人應徵

4/30 臨床試驗專員 (Clinical Research Associate, CRA)

  • 台北市內湖區
  • 1年以上
  • 碩士

1. 協助臨床試驗執行，包括試驗之聯繫與回報、行政作業執行。 2. 聯繫合作的CRO公司與醫院臨床試驗團隊，跨部門協調與溝通。 3. 臨床試驗法規申請審查資料準備，與國內外法規相關單位溝通聯繫。 4. 進度報告彙整。 5. 臨床試驗相關資料整理與文件管理撰寫、歸檔 6. 其他主管交辦事項。

月薪38,000~45,000元 距捷運西湖站約500公尺
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6~10人應徵
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