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Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include m
This unique role within IQVIA lends itself to a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication and organisation skills. Having experience with SAS programming is necessary. This role is part of a sponsor dedicated project wher
Job Overview Lead and support effective corrective and preventive action (CAPA) management for significant quality issues (QIs) and audit and inspection responses including the assessment and review of investigations, appropriate root cause analysis and corrective and preventati
Associate Principal / Manager, Data & Analytics Consulting •製薬企業の組織体制および業務設計の現状評価と戦略的改善策のシナリオを設定し、ファイナンシャルモデルを用いて営業活動効率の最適化プラン検討します •製薬企業の営業拠点毎の市場性やMR活動量に応じた、最適なMR配置計画をします •医療に関わる様々なステークホルダーに対し、医療圏毎の薬物治療介入の実態の分析などを通じて、医療課題の解決に繋がる提言も行っています ・在宅勤務制度:あり ・福利厚生:法定内&#x
requests and studies, including oversight of technical processes and procedures insofar as they impact pathology interpretations. Perform microscopic analyses of laboratory assays and monitor digitization of slides. Correlate clinical information with pathology findings. Release
Job Overview Responsible for performing a variety of technical procedures and experimental execution in support of sample analysis and validation. Responsible for root cause analysis, troubleshooting, and supporting process improvements. Essential Functions • Responsible for per
Job Overview Support the purchasing processes in accordance with policy and procedures. Ensure adherence to the IQVIA Transnational corporate purchasing policy which encourages vendor competition. • Extract spend data from accounts payable or other databases and create spend re
Job Summary: This position is responsible for the development of the end-to-end design of client standards and study specifications that align to the CDISC standards and regulatory agency guidance’s. Support clients and IQVIA as an authority in the use of CDISC Standards throug
Job Overview Senior .Net Software Engineerwrites well-designed, testable, and efficient codes as part of the development team and will work under the supervision of managers of Population Health. - - Provide technical guidance in planning and executing assigned projects - -
- 工作职责 - 协助主管处理药品不良反应安全数据,包括:收集和跟踪传入的不良事件(AE)/终点信息、确定传入事件的初始/更新状态、跟踪事件处理完成的时间表等工作。 协助主管管理项目工作流程,包括数据库录入、质量控制活动和药品安全数据报告的生成,准备药品安全提交档案等工作。 其他主管指派的协助任务等。 - 任职要求 - 实习地点 - *接受远程和线下实习相结合的方式 - 顺利通过实习期考核即可优先得到正式offer。
• 作为研究团队成员,遵照法规要求、商定的工作范围、适用的SOP、工作授权和试验方案,在 研究中心进行工作。 • 协助研究者完成可行性调查问卷和回收问卷。 • 推动研究中心启动工作:协助研究中心筛选访视,协助及时提交文件到伦理委员会进行审批 和试验用药品的发放,协助研究中心启动访视。 • 协助研究者进行受试者筛选和入组研究。 • 得到研究者授权后,根据法规和GCP的要求,协助研究者顺利完成方案要求的随访和步骤:如 制定计划、清点核对药品
Job Summary The Research Laboratory Technician is responsible for performing routine analysis and laboratory testing procedures. Essential and other important responsibilities and duties may include but are not limited to the following: - Label, receive, and process samples (b
Help shape the future of ILD care. We are looking for a strategic and collaborative ILD Transformation Advisor to support the assessment, design, and potential expansion of an international healthcare program focused on Interstitial Lung Disease (ILD). In this role, you will wo
IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundhei
Job Overview Provide project related support; assist with designing, loading, and validation of Lab databases using Clinical Trials Management System(s); ensure work is conducted in line with standard operating procedures, policies and good practice. Accountability and ownership
“Ce message est publié en prévision d'un rôle futur." Niveau : Biostatisticien principal FSP pour la recherche en données probantes en vie réelle Lieu : Télétravail aux États-Unis ou au Canada Solutions d'entretien des sciences des données (DSSS), une entité d'IQVIA, met à la
We are seeking an experienced PK/PD Statistical Programmer with strong experience in R programming, PK/PD datasets, and NONMEM dataset creation. This role supports Pharmacometrics by producing high‑quality, compliant datasets for modeling and analysis, ensuring accuracy from earl
This position will put you at the forefront of Patient Safety. As a MI/PV agent (dual role) you will have daily direct contact with Health Care Professionals (HCPs) and patients (the very people we are working to help), this is a highly visible and important role within IQVIA and
- Develop basic market research skills / competencies via on-the-job learnings and class-room trainings. - Support project team on overall execution of market research project to ensure timely delivery and assist in proposal preparation. - Assist in drafting research materia
Job Description Summary Responsible for study build & design, edit specifications, system configurations and is accountable for associated study design components. This role will collaborate with various stakeholders- DTL, Programmer, Validation Team, vendors, statisticians, and
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