iqvia

Join a global healthcare leader where innovation, purpose, and professional growth come together. At IQVIA, you'll gain exposure to leading pharmaceutical and biotechnology organizations, diverse therapeutic areas, cutting-edge technologies, and meaningful work that helps improve patient outcomes wh

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 preventative actions. Provide s

About the role As a (Senior) Consultant in our Market Access & Health Economics team, you will support pharmaceutical and MedTech clients turn evidence into patient access. You will lead workstreams, write and review reimbursement dossiers, develop and adapt budget impact and cost-effectiveness mode

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. Job Responsibilities: Support clients and IQVIA as an authority in the use of CDISC Standards throug

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 early (unclean) through

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 Gesundheitswesen darin, besse

Job Overview We are looking for a skilled Data Analyst with strong experience in data analysis, querying, reporting, and data validation across cloud and database platforms. The ideal candidate should have hands-on knowledge of Snowflake, Azure platform services, and Oracle databases, with the abili

Job Overview Perform 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 (RS

Role Purpose Ensure the accuracy, completeness, and consistency of data during the production of IQVIA Belgium information assets. Investigate challenges, analyze complex business problems and make recommendations to improve on data quality and procedures whilst applying best practices Support comme

POSITION PURPOSE Drive the strategic workflow activities daily, provide support and expertise in the production of assigned IQVIA data assets Coordinate with other offshore teams to deliver high quality outputs on time Run data quality and integrity steps across the multi production streams, includi

AI Engineer/Scientist Job Overview Develop fit for purpose AIML models/algorithms/processes to address pharma/healthcare applications and innovative products upon completion of prototypes followed by the building of production grade algorithms/automation engines for client deliverables. Test for via

The Local Clinical Project Manager (Sponsor dedicated) will be leading Local Study Teams at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Sponsor Procedural Documents, international guidelines such as ICH-GCP as w

Job Overview IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the product lifecycle. The Patient Centered Solutions (PCS) team leads the industry in generating data to ensure that the patient voice is incorporated into the development a

Job OverviewResponsible for the on-time completion of projects or components of large, complex projects for clients in the life sciences field. Identifies and elevates potential new business opportunities and assists in the sales process.Essential Functions• Participates or leads teams in the design

工作职责1.协助完成实习生招聘全流程，包括简历筛选、面试安排及录用跟进，保障招聘效率。2. 负责招聘系统的简历信息维护与数据更新，确保人才库的准确性与完整性。3. 参与内部推荐活动的物料制作，如设计宣传文案、制作PPT等，提升招聘渠道影响力。4. 整理并制作各类人事表格，完成员工信息归档与数据统计工作。5. 配合部门同事完成其他人力资源相关事务性工作，支持团队日常运营。任职要求1.本科及以上学历，2027届毕业生，人力资源管理、工商管理等相关专业优先。2. 每周可实习3天以上，能连续出勤4个月及以上，保证工作稳定性。3. 熟练使用Excel、PPT等办公软件，具备基础的数据处理与文档制作能力。

工作职责： 1. 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。 2.协助研究者完成可行性调查问卷和回收问卷。 3.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。 4.协助研究者进行受试者筛选和入组研究。 5.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、清点核对药品和其他协调工作。 6.在研究中心协助研究者管理试验用药品、研究物资和实验室样本。 7.在商定的工作范围内，参加研究者会、监查访视、稽查和其他会议。 8.

Job Overview Under general guidance, develops and executes test plans and scripts to confirm the quality and success of various technologies. Manual and automated testing of applications and web resources works as specified; ensures a system performs adequately deployed platform. Essential Functions

Opportunity in a dynamic multi‑sponsor environment - we are looking for experienced CRAs for our Site Management Team in Poland! Responsibilities Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory require

Global Biostatistics Job Level: Statistical Scientist Location: Home-based in the U.S / Canada Join us on our exciting journey! The Global Biostatistics (Data Sciences, Safety & Medical) team at IQVIA are experienced in submissions for all major regions; working together with key groups such as, Glo

Job Overview Independently manage end-to-end delivery of data management services for single/multi-service projects, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide hi