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Researcher/Scientist_Lab-Large Molecule

  • 台北市南港區
  • 3年以上
  • 大學

The Researcher is responsible for the conduct of analysis related works according to GCP, GLP, CAP, Standard Operating Procedures (SOP), applicable Study Specific Procedures (SSP), and local regulatory requirements. Manage the operation of MT and aid physicians in the diagnosis, treatment, and prevention of diseases by testing patient specimens, correlating data, and reporting results in a timely manner to effect quality patient care. Responsibilities: Perform analysis work according to SOPs and guidance. Prepare, review, and approve various documents, including SOPs, protocols, reports, and analytical methods. Manage lab logistics, including purchasing, inventory control, and payment processing. Maintain instruments and ensure cleanliness and maintenance of the workspace. Take on the role of system owner for computerized systems, performing tasks such as validation tests, periodic reviews, and reporting. Attend training courses related to CAP/GCP/GLP/regulatory requirements. Study Based Responsibility (if needed) Analytical Study Director in Study Work as the Study Director, responsible for the overall conduct and final report of the study. Approve the study plan and any amendments by signature, and ensure Quality Assurance personnel receive timely copies. Make study plans, amendments, and SOPs available to study personnel. Ensure procedures in the study plan are followed and document deviations and take corrective action if necessary. Document and record all generated raw data. Validate computerized systems used in the study, sign and date the final report to indicate acceptance of responsibility for data validity, and ensure study materials are archived after completion. Study Personnel in Study Ensure personnel are knowledgeable in relevant Principles of Good Laboratory Practice. Provide study personnel with access to study plans and SOPs applicable to their involvement, with a responsibility to follow instructions and document any deviations. Emphasize the responsibility of all study personnel to promptly and accurately record raw data, comply with Good Laboratory Practice principles, and exercise health precautions to safeguard the integrity of the study.

待遇面議 員工2000人 距捷運南港軟體園區站約430公尺
0~5人應徵

5/10 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

5/10 工研院產科國際所_實證醫學與臨床試驗組研究員(A0100衛福部團隊)

  • 台北市南港區
  • 經歷不拘
  • 碩士

工業技術研究院 國際級的應用研究機構，擁有六千位研發尖兵，以科技研發，帶動產業發展，創造經濟價值，增進社會福祉為任務。 工研院產業科技國際策略發展所(簡稱:產科國際所) 是政府與產業均仰賴的智庫，結合產業研究與國際業務推動能量，以協助台灣產業布局全球市場為己任，以『促進台灣產業科技創新與價值提升』為願景。 旗下經營的IEK產業情報網已超過15年歷史，是國內產業情報資料庫的領導品牌。 IEK產業情報網：http://ieknet.iek.org.tw/ 工作內容: 因應醫療AI產業發展之產品驗證與保險給付之所需，負責擬定臨床實證醫學AI相關指南，協助建立台灣醫療AI發展基礎。 工作地點:台北生技園區(115台北市南港區忠孝東路七段508號) 歡迎您加入團隊，成為未來智慧醫療產業儲備領袖人才！

待遇面議 員工6000人 遠端工作 距捷運南港站約270公尺
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6~10人應徵

5/10 臨床法規助理 Clinical Trial

  • 台北市大安區
  • 1年以上
  • 大學

[工作職責] - 臨床試驗計畫書設計及報告撰寫 - 臨床評價報告撰寫(clinical evaluation report, CER) - 文獻搜尋&閱讀 - 臨床試驗/文獻數據 整理&分析 - 各國不良事件資料庫搜尋及整理 - 各國醫療器材法規整理 - 完成主管交辦的工作 - 視需要需短期出差 [任職要求] - 醫學相關背景(包含公衛學系)尤佳 - 有臨床試驗相關經驗者優先 - 需具有文獻搜尋經驗 - 需具有基本統計概念 - 熟練運用Word、Excel、PowerPoint等文書處理軟體 - 積極進取，有責任感 - 能獨立作業也可配合團隊合作 - 需外出出差 (當天來回)

待遇面議 員工100人 距捷運忠孝新生站約180公尺
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0~5人應徵

5/10 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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11~30人應徵

5/10 Medical Science Liaison

  • 台北市信義區
  • 2年以上
  • 大學

POSITION SUMMARY - This position is responsible for marketing biosimilar products (Immunology and Oncology) through strategic planning and effective marketing mix with optimization of communication/engagement. - Build medical Strategy for biosimilar, define the high-level medical communication plan and focus on key operational tactics to address the needs of different external stakeholders. - Work in collaboration with the sales team as key contact for external experts and execute the medical/marketing activities related to area of responsibility with a focus on defining & implementing a multichannel strategy. KEY ROLES AND RESPONSIBILITIES 1. Medical Marketing strategy development & implementation - Propose/implement product strategies by understanding market unmet needs - Construct strong network with key opinion leader - Develop key opinion leaders and closely bidirectional communication - Make congress management plan and collaboration - To work with KOLs to identify topics of interest to the medical community and in alignment with TA identified scientific interests and provide scientific support to the development of TA strategic plans. - To serve as primary Medical Affairs contact with key academic and community-based medical coordinating with sales team to help engage potential key medical leaders. Cross function communication 2. Engagement excellence to optimize brand performance - Develop key message and programs with patient centricity - Communicate product benefits to all the relevant customers (HCP, Patients, Payer, Internal) effectively - To provide scientific support at medical information exhibits at medical conferences and meetings (such as Advisory Board meetings…etc.) to identify and effectively communicate new opportunities/threats that have an impact on the product portfolios - Provide product advocacy through facilitating literature searches, slide creation, and presentations to various external customers. - Present approved scientific data to healthcare providers in both group and one-on-one settings by company policies, applicable laws, regulations, and ethical standards. - Maintain clinical, scientific, and technical expertise in the specific therapeutic area and in-depth and up-to-date knowledge of products across the internal and competitor portfolios. 3. Development of communication and education programs - Analyze available market data & intelligence to monitor brand performance and to define key issues & opportunities - Collaborate with team to develop business plan for each specialty with product franchise - Identify new opportunities consistently to maximize efficacy of KOL engagement and brand communication - Prioritize resource allocations through Segmentation & Targeting

待遇面議 員工40人 距捷運象山站約380公尺
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0~5人應徵

5/10 Senior Clinical Research Associate- FSP Global TOP Pharma

  • 台北市信義區
  • 3年以上
  • 大學

** Very competitive package ** - Primary point of contact between site staff and the company. Acts as ambassador for the company and contributes to making company the preferred partner. - Responsible for taking leadership of site management for the selection and initiation of sites as well as conduct and closing activities of the appointed studies in compliance with local regulations, ICH- GCP, company procedures and protocol requirements to ensure data quality and study subject protection. - Responsible for managing the site to meet patient recruitment rate and target. - Delivers results that have direct impact on the successful completion of the clinical programm. - Coordinates with LTM and RTM and communicates to them progress and critical issues that may impair trial progress.

待遇面議 外商公司 員工300人 遠端工作
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0~5人應徵

5/09 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

5/09 Regulatory Start-up Associate

  • 台北市中山區
  • 1年以上
  • 大學

Please do submit English resume to our company website. https://fa-euzi-saasfaprod1.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/requisitions/preview/2468/?mode=location Brief Position Description: The Regulatory Start Up Associate is primarily responsible for planning, preparation, review of country and site level ethics and regulatory authority applications and submissions during project start-up, in compliance with ICH-GCP and local regulatory requirements, to ensure timely clinical trial approval. Core Responsibilities: Serve as the primary point of contact for the Regulatory Start Up Manager (RSM) and/or Project Manager (PM) during start-up on allocated projects. Provide expertise and guidance to RSM and/or PM on country and local regulations and practices, keeping abreast of developments and changes in regulations, guidelines and practices surrounding clinical trial approvals in relevant countries. Work within the scope of the Regulatory Start Up plan or other applicable project plan, relevant SOPs, and ICH-GCP. Provide country and site level information on submission deadlines and timeline metrics for local Regulatory Authority, Ethics Committees, Investigational Review Boards and other local bodies as appropriate. Works within forecasted submission/approval timelines and ensures they are complied with, updating appropriate systems accurately and in a timely manner, including planned and actual dates of submissions/approvals. May serve as a point of contact with investigative sites for Regulatory Authority, Ethics Committees/Review Boards and other local authority related activities. Prepare and submits Central EC/IRB applications, local EC/Governance applications, Regulatory Authority applications, and other local regulatory authorities or site submissions as required. >Ensure submission packages are accurate and complete per local requirements. >Review and follow-up on comments/questions raised by reviewing bodies and advise/contribute to response. Submit response with Client approval within timeframe. >Follow submission, application to approval. May serve as a point of contact for Regulatory Authorities, Ethics Committees/Review Boards and other local authorities. Prepare and submit ongoing amendments, notifications, safety reports and study related materials required by Regulatory Authorities, Ethics Committees/Review Boards and other local authorities as per local requirements. Escalate any issue to the RSM and/or PM and provides rationale for submission/approval delays, and contingency plan to mitigate impact. Perform country and site Informed Consent Form (ICF) customisation in line with local requirements. Initiate translation of submission documents as applicable and review translated documents before submission. Review and approve proposed packaging and labelling for clinical trial material. Prepare and submits import/export license applications and management of licenses and custom clearance thereafter if required. Register project onto an official clinical trial registry as agreed to with Client and update status as required. Submit regulatory and ethics documents and relevant study correspondence to the trial master file and ensures accuracy and completeness of these documents. Serve as an independent essential document reviewer and performs 2nd review of Activation Forms for IP release if required. Where applicable, may act as a Country Lead for projects with no RSM.

待遇面議 員工2000人 遠端工作 距捷運中山站約300公尺
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0~5人應徵

5/09 (Senior) Clinical Research Associate (CRA)

  • 台北市松山區
  • 1年以上
  • 大學

Job Overview: Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions: • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. • Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability. • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. • Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. • Collaborate and liaise with study team members for project execution support as appropriate. • If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. • If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

待遇面議 外商公司 距捷運中山國中站約470公尺
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0~5人應徵

5/09 Lab Project Manager

  • 台北市南港區
  • 3年以上
  • 大學

Please do submit English resume via our company website. https://fa-euzi-saasfaprod1.fa.ocs.oraclecloud.com:443/hcmUI/CandidateExperience/en/job/2281?utm_medium=jobboard Reporting to: Lab PM Head Position description: Responsible for the overall management of laboratory projects to ensure the adherence of the project to applicable quality standards ( GLP, CAP, GCP), approved timeline and budget in the service agreements. Lead the project team, manage internal/external communications, and identify suitable resources to facilitate efficiency improvement for project execution. Responsibilities: Responsible for the overall project planning and execution of the project per agreed timeline, budget, scope, and quality regarding the assigned projects. Ensure accurate and timely communication with customers regarding delivery of work product and project progress. Ensure that project members have the proper materials, systems access and training to complete project job responsibilities. Responsible for project tasks, including but not limited to lab documents development, bio sample import/ export permits application, query management, project status tracking, management and reporting. Identify quality issues within the study to implement appropriate corrective action plans. Escalate findings and action plans to appropriate parties. Participate and contribute to the BD project bidding and marketing activities, and to facilitate the success of business explore and contract award. Take on additional responsibilities that may be assigned by the line manager. Qualifications: Minimum of a Bachelor's degree or equivalent in Science or medical related filed. Three (+) years relevant work experience in the GLP/ clinical laboratory operations or project management is preferred. Skills and Competencies: Familiar with laboratory related activity processes throughout a clinical trial with good knowledge in GLP, CAP and local regulations. Excellent customer management and problem resolving skills. To be proactive, flexible, organized, and aim to mitigate risk, understanding plans and outcomes fluctuate, and be highly communicative during the entire process. Strong communication and interpersonal skills, fluent communication of speaking and writing in English is preferred. Demonstrated ability to deliver results to the appropriate quality and timeline metrics. Strong software and computer skills, including MS Office applications.

待遇面議 員工2000人 遠端工作 距捷運南港軟體園區站約430公尺
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0~5人應徵

5/09 Senior Technical Support Specialist

  • 台北市中山區
  • 經歷不拘
  • 碩士

Responsibilities: 1.Strong technical communication ability,able to cooperate with BD to visit customers,arrange online and offline technical communication according to customer needs,and answer customers' technical questions; 2.Be responsible for the quotation of bioanalysis and Central lab business. Quick response of quote generation within the technical support department for most customer needs; For complex projects,able to effectively coordinate other teams inthe lab to conduct internal communication and evaluation and finalize the plan; 3.Assist the bioanalysis and central lab in project research,data query and competitor analysis of related technology platform construction; 4.Cooperate with the commercial team to prepare the technical bid,answer and explain the technical questions of the bid; 5.Complete other matters temporarily assigned by leaders. Minimum Qualifications & Experience: 1.Master degree or above in pharmacology,biology,biotechnology,bioengineering,immunology,medicine and other related majors; 2.Experience in lab business of clinical CRO company is preferred; 3.Solid professional foundation,strong logic analysis ability,and be able to masterclinical trial related testing knowledge after training; 4.Have a certain understanding of the regulatory requirements and guiding principles of NMPA/FDA and ICH,especially on bioanalysis and central lab related testing;

月薪55,000~70,000元 員工2000人 距捷運中山站約320公尺
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0~5人應徵

5/09 (Associate) Regulatory Operations Manager

  • 台北市中山區
  • 5年以上
  • 大學

Please do submit English resume to our company website. https://fa-euzi-saasfaprod1.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/2487 Brief Position Description: Associate Regulatory Operations Manager provides supervision, leadership, and line management of the Regulatory Start up team. This role will ensure that line reports are trained and managed to regulatory start-up process including regulatory authority (RA) and ethics committee (EC) submissions and approval and site identification according to ICH-GCP guidelines, local regulatory requirements, Novotech / client standard operating procedures (SOPs), and the Project Agreement. Responsibilities: Line Management - Act as line manager for one or more assigned staff; serve as a designated mentor to assigned regulatory start-up operations staff. - Ensure line reports are aware and understand company policies and procedures appropriate to their position. - Meet regularly (in probation weekly or bi-weekly upon LM’s decision, moving to a minimum of monthly) with line reports to review their workload, welfare, and developmental needs. - Ensure management is aware of line report performance progress and informed of any issues arising. Project Execution and Delivery - Work alongside line reports by oversight, planning, preparation, reviewing and approving of EC and RA applications to ensure timely approval of clinical trials. - Review and approve proposed packaging and labelling for investigational products. - Preparation, review, and submission of importation and/or exportation licences and/or permits for investigational products. - Preparation, review, and approval of essential documents such as Participant Information Sheets and Consent Forms. - Review of Regulatory Green Light for Investigational Product Release package - Develop and maintain tracking to ensure status of work and progress towards timelines is clearly documented and available to project teams. Monitor functional performance metrics.

待遇面議 員工2000人 遠端工作 距捷運中山站約320公尺
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0~5人應徵

5/09 醫事檢驗師 Medical Technologist_Lab-Central Lab

  • 台北市南港區
  • 2年以上
  • 大學

如果你是一位擁有醫檢師執照的專業人才，如果你對臨床試驗的檢驗分析有高度熱情，如果你渴望挑戰自我，我們需要你！ 我們正在尋找一位積極、具有創造力並對於檢驗分析充滿熱情的醫事檢驗師加入我們的團隊。作為我們的醫事檢驗師，你將可以在醫事檢驗所執業登記，並參與到檢驗前、中、後的活動。除了提供良好的工作環境並有免費的零食餵食以外，還有完善的教育訓練制度，我們同時擁有一個已有20多年美國病理學會(CAP)認證歷史的醫學實驗室，並致力於不斷提升自我，為臨床試驗中的受試者提供最好的檢驗服務。 如果你擁有兩年以上的醫事檢驗師資歷，並在流式細胞儀分析、分子生物、病理檢驗染色、手工血清學有檢測或是方法開發經驗，那麼這是一個絕佳的機會，請盡快加入我們的團隊。同時，如果你擁有ISO-15189受訓證書或是有至少參加過一次CAP inspection的經驗，更是加分。 此外，我們歡迎積極、樂觀、勇於接受挑戰的個性的人加入我們的團隊。如果你渴望或是尋求機會可以跨足生技產業的行業展現自我，希望通過不斷學習和提高提升自我，那麼這將是一個絕佳的工作機會。如果你想脫離單調的醫院工作環境，請加入我們的團隊，開始一段全新的職業生涯。放下手中的鍵盤在靠北醫檢師社團的抱怨，期待你的加入！ If you are a licensed medical technologist with a passion for clinical trial testing and a desire to challenge yourself, we need you! We are looking for a proactive, creative and passionate medical technologist to join our team. As our medical technologist, you will be able to register for practice in the medical laboratory and participate in pre-analytical, analytical, and post-analytical activities. In addition to providing a good working environment and free snacks, we have a well-established educational training system and a clinical laboratory that has been certified by the College of American Pathologists (CAP) for more than 20 years. We are committed to continuous improvement and providing the best testing services for clinical trial subjects. If you have more than two years of medical technologist experience and have method development or analysis experience in flow cytometry analysis, molecular biology, pathology staining, and manual serology testing, this is an excellent opportunity to join our team. Furthermore, if you have an ISO-15189 training certificate or have participated in at least one CAP inspection, that's a plus. In addition, we welcome individuals with positive, optimistic, and challenge-accepting personalities to join our team. If you are eager or seeking opportunities to step into the biotech industry and show your talents through continuous learning and improvement, then this will be an excellent job opportunity. If you want to break away from the monotony of hospital work environments, join our team and start a new career.

待遇面議 員工2000人 距捷運南港軟體園區站約430公尺
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0~5人應徵

5/09 (Senior) Scientist_Lab-Small Molecular

  • 台北市南港區
  • 1年以上
  • 大學

Please do submit English resume via our company website. https://fa-euzi-saasfaprod1.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/2284?utm_medium=jobboard Reporting to: Lab Director, or Lab Manager Position Description: The Researcher is responsible for the conduct of analysis related works according to GCP, GLP, CAP, Standard Operating Procedures (SOP), applicable Study Specific Procedures (SSP), and local regulatory requirements. The report writer/QC is responsible for writing correspond study report/method according to study plan and Standard Operating Procedures (SOP). And to perform the quality control works. Responsibilities: General Responsibilities • Conduct analysis work following related SOPs and guidance. • Draft/check/review/approve documents, such as SOP, protocol, analytical result, report and method. • Involve in lab logistics (general affair) management, such as purchasing, inventory controlling, payment applying. • Responsible for instrument maintenances, workspace cleaning/maintenance. • Delegated /assigned as the system owner for computerized system, do the corresponding work for system, such as validation test, periodic review, report, etc. • Participate in CAP/GCP/GLP/ regulatory related training courses. • Provide temporary supporting assigned by line manager. • Refer to additional Study Based Responsibilities while being assigned in analytical project. • Involve in sample collection kit/label preparation. • Involve in analytical study project management. • Other tasks assigned by line manager. Study Based Responsibility (if needed) Study Personnel in Study • All personnel involved in the conduct of the study must be knowledgeable in those parts of the Principles of Good Laboratory Practice which are applicable to their involvement in the study. • Study personnel will have access to the study plan and appropriate Standard Operating Procedures applicable to their involvement in the study. It is their responsibility to comply with the instructions given in these documents. Any deviation from these instructions should be documented and communicated directly to the Study Director, and/or if appropriate, the Principal Investigator(s). • All study personnel are responsible for recording raw data promptly and accurately and in compliance with these Principles of Good Laboratory Practice, and are responsible for the quality of their data. • Study personnel should exercise health precautions to minimize risk to themselves and to ensure the integrity of the study. They should communicate to the appropriate person any relevant known health or medical condition in order that they can be excluded from operations that may affect the study. Report Writer/Quality Control • As QC person, check and review the study data, document, report. • Involve in reference compound management, such as planning, shipping, receiving, using, storing, and disposing. And as the backup of sample manager. Qualifications: Education and Experience: • Secondary Technical school, Junior colleague, BS (Bachelor of Science) degree in Biochemistry, Biotechnology and Laboratory Science, Chemistry, or a related field. Advanced degree is a plus for Associate Researcher/ Senior Researcher. • License of Medical Technician is required for Associate Researcher/ Senior Researcher in Central Lab. Skills and Competencies: • Familiar with all lab operation activities. • Good working knowledge of CAP/GCP/GLP, applicable law (local and country) and regulatory requirements. • Good communication skills. • Good verbal and written English or other second language skills. • Good problem-solving skills. • Effective time management and prioritization skills.

待遇面議 員工2000人 距捷運南港軟體園區站約430公尺
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0~5人應徵

5/09 (Senior) Clinical Project Manager

  • 台北市松山區
  • 6年以上
  • 大學

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward. One of FORTUNE’s ‘Most Admired Companies’, we offer unparalleled scope for a career in world-leading clinical research. Global projects, innovative tools and industry leading customers combine with outstanding support and clear career management which allows you to make a difference and to connect with great opportunities. While projects vary, your typical responsibilities might include: Manage and co-ordinate efforts of cross-functional project teams to support milestone achievement and to manage study issues and obstacles and ensure consistent use of study tools and training materials and compliance with standard processes, policies and procedures. - Develop study management plans, together with team assignments and accountabilities and oversight of database maintenance. - Serve as primary project contact with Sponsor to ensure communication is maintained and reporting schedules are adhered to. - Collect information on team performance against contract, customer expectations, and project baselines. - Lead problem solving and resolution efforts to include management of risk, contingencies and issues. - Identify quality issues within the study to implement appropriate corrective action plans. Escalate findings and action plans to appropriate parties. - Provide input for the development of proposals for new work and manage project budgets. - Provide input to line managers of their project team members’ performance relative to project tasks. - Prepare and present project information at internal and external meetings. - Participate in proposal development and in the bid-defense process with guidance and supervision. - Ensure high performance and efficiency of the clinical team through the scheduling of co-monitoring/accompanied site/visits and ongoing mentoring of CRA team. You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally you will also have some global experience, and a pharmaceutical or CRO background.

待遇面議 外商公司 距捷運中山國中站約470公尺
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0~5人應徵

5/08 【英商醫藥原廠】Market Access Specialist (LLS_834)

  • 台北市大安區
  • 2年以上
  • 大學

【Key Responsibilities】 • Responsible for optimizing introduction of new drugs, assist in department managers to identify market access strategies in cooperation with cross functional teams, ensuring right and effective ways to articulate product value story. • Prepare responsible product reimbursement cases, including but not limited to launch preparation, dossier submission, budget impact analysis, cost-effectiveness analysis (if needed), follow-up negotiations and agreements. • Assist in performing analysis related to price forecast, estimate price cut, validate financial clawback/ rebate, and support department managers for government agency communication and negotiations. • Assist in analyzing market trends of pharmaceutical industries and related healthcare policies. • Assist in driving market access agenda in close collaboration with internal and external key stakeholders. 有興趣者可投遞履歷至 [email protected] 或致電 02-7718-8834 Andy

月薪40,000~65,000元
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0~5人應徵

5/08 研究員(藥理研究)

  • 台北市南港區
  • 3年以上
  • 博士

*因應集團擴編需求，新增具備藥理研究能力之職位 1.          設計實驗、使用免疫學相關技術分析人類及小鼠檢體 2.          設計並執行人類檢體體外培養實驗 3.          開發生物活性分析方法 4.          分析數據及撰寫報告 5.          實驗室行政事務 6.          收集、整理最新學術文獻，定期報告 7.          主管交辦事項   附註: 具免疫學背景尤佳

待遇面議 距捷運南港軟體園區站約420公尺
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0~5人應徵
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