IQVIA

MCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and diagnostics industry. Together we support innovation from concept to commercialization offering expertise in regulatory strateg

MCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and diagnostics industry. Together we support innovation from concept to commercialization offering expertise in regulatory strateg

We are seeking Scientific Advisor Director to join IQVIA Laboratories at Austin TX (Remote).We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose join us as we transform and acce

We are seeking Scientific Advisor Director to join IQVIA Laboratories at Austin TX (Remote).We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose join us as we transform and acce

We are seeking Clinical Trial Material Manager (2nd Shift) to join IQVIA Laboratories at Marietta GA.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose join us as we transform

We are seeking Clinical Trial Material Manager (2nd Shift) to join IQVIA Laboratories at Marietta GA.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose join us as we transform

Account Manager Small PharmaAbout the RoleIQVIA is a global leader in advanced analytics technology solutions and clinical research for the life sciences industry.We are currently seeking an Account Manager to support our Small Pharma Segment managing a portfolio of approximately 2030

Account Manager Small PharmaAbout the RoleIQVIA is a global leader in advanced analytics technology solutions and clinical research for the life sciences industry.We are currently seeking an Account Manager to support our Small Pharma Segment managing a portfolio of approximately 2030

IQVIA is hiring to expand our dedicated Real-World Evidence (RWE) FSP team working fully within the environment of a prominent pharmaceutical company. This senior data analyst role sits within our Data Science Analytics and Technology Solutions (DATS) team and will be responsible for

IQVIA is hiring to expand our dedicated Real-World Evidence (RWE) FSP team working fully within the environment of a prominent pharmaceutical company. This senior data analyst role sits within our Data Science Analytics and Technology Solutions (DATS) team and will be responsible for

IQVIA is hiring to expand our dedicated Real-World Evidence (RWE) FSP team working fully within the environment of a prominent pharmaceutical company. This senior data analyst role sits within our Data Science Analytics and Technology Solutions (DATS) team and will be responsible for

IQVIA is hiring to expand our dedicated Real-World Evidence (RWE) FSP team working fully within the environment of a prominent pharmaceutical company. This senior data analyst role sits within our Data Science Analytics and Technology Solutions (DATS) team and will be responsible for

About IQVIA:IQVIA is a fast-growing and highly successful business delivering data-driven insights and measurable impact for clients across the global life sciences ecosystem. Leveraging access to some of the worlds most comprehensive healthcare data advanced analytics and research ca

About IQVIA:IQVIA is a fast-growing and highly successful business delivering data-driven insights and measurable impact for clients across the global life sciences ecosystem. Leveraging access to some of the worlds most comprehensive healthcare data advanced analytics and research ca

We are seeking a highly motivated pharmacovigilance professional to join our Safety Aggregate Report & Analytics (SARA) team. This is an exciting opportunity to take a leading role in safety reporting signal management and benefit-risk evaluation activities supporting both marketed an

We are seeking a highly motivated pharmacovigilance professional to join our Safety Aggregate Report & Analytics (SARA) team. This is an exciting opportunity to take a leading role in safety reporting signal management and benefit-risk evaluation activities supporting both marketed an

Provides high quality timely development and on-time input to client solutions for the pharmaceutical and related industries. Assignments range in complexity from basic analysis and problem solving to assisting in the development of more complex solutions to leading small teams.Essent

Provides high quality timely development and on-time input to client solutions for the pharmaceutical and related industries. Assignments range in complexity from basic analysis and problem solving to assisting in the development of more complex solutions to leading small teams.Essent

Provides high quality timely development and on-time input to client solutions for the pharmaceutical and related industries. Assignments range in complexity from basic analysis and problem solving to assisting in the development of more complex solutions to leading small teams.Essent

Provides high quality timely development and on-time input to client solutions for the pharmaceutical and related industries. Assignments range in complexity from basic analysis and problem solving to assisting in the development of more complex solutions to leading small teams.Essent

Job Overview 根据国内外药物警戒相关法规及公司内部的药品安全信息管理的相关规定管理收集本公司和其他公司同类产品必要时的临床试验及上市后安全信息 对安全报告处理及递交进行质量审核包括安全性报告在数据库中的处理以及药品安全性信息报告过程中的翻译等 在规定时限内将药品安全信息报告给监管机构以及其他相关方并对相关文件进行维护和归档 根据需要撰写并更新具体实施过程中的相关文件如临床试验中安全管理计划SMP培训材料等项目相关材料 审阅临床试验项目及上市后项目的相关文件如临床试验方案研究者手册IB等 支持或撰写药物警戒汇总性报告如研发期间药物安全性更新报告DSUR定

Job Overview 根据国内外药物警戒相关法规及公司内部的药品安全信息管理的相关规定管理收集本公司和其他公司同类产品必要时的临床试验及上市后安全信息 对安全报告处理及递交进行质量审核包括安全性报告在数据库中的处理以及药品安全性信息报告过程中的翻译等 在规定时限内将药品安全信息报告给监管机构以及其他相关方并对相关文件进行维护和归档 根据需要撰写并更新具体实施过程中的相关文件如临床试验中安全管理计划SMP培训材料等项目相关材料 审阅临床试验项目及上市后项目的相关文件如临床试验方案研究者手册IB等 支持或撰写药物警戒汇总性报告如研发期间药物安全性更新报告DSUR定

Senior CRA 1 - Sponsor DedicatedGauteng basedJob OverviewAs a Sponsor-Dedicated Senior Clinical Research Associate I (Sr CRA I) you will be responsible for monitoring and managing clinical trial sites for a dedicated sponsor ensuring studies are conducted in compliance with protocol r

Senior CRA 1 - Sponsor DedicatedGauteng basedJob OverviewAs a Sponsor-Dedicated Senior Clinical Research Associate I (Sr CRA I) you will be responsible for monitoring and managing clinical trial sites for a dedicated sponsor ensuring studies are conducted in compliance with protocol r

IQVIA Digital powers exceptional brand experiences delivering innovative solutions based on a customer-first insights-driven and integrated omnichannel provide authenticated privacy-enhanced data and analytics innovative fit-for-purpose healthcare technology and the expertise to enab

IQVIA Digital powers exceptional brand experiences delivering innovative solutions based on a customer-first insights-driven and integrated omnichannel provide authenticated privacy-enhanced data and analytics innovative fit-for-purpose healthcare technology and the expertise to enab

OverviewCustomer dedicated Clinical Project Management Director taking an Indication Director role to provide operational delivery oversight for select indication(s). Provides strategic and operational leadership for indication-level delivery translating strategy into effective execut

OverviewCustomer dedicated Clinical Project Management Director taking an Indication Director role to provide operational delivery oversight for select indication(s). Provides strategic and operational leadership for indication-level delivery translating strategy into effective execut

Senior Consultant Tech IQVIA Inc. Wayne PA. Must telecommute from anywhere in the US and report electronically to the Wayne PA office. Work with business users to elicit functional and technical requirements on assigned health and life science industry projects. Lead the overall desig

Senior Consultant Tech IQVIA Inc. Wayne PA. Must telecommute from anywhere in the US and report electronically to the Wayne PA office. Work with business users to elicit functional and technical requirements on assigned health and life science industry projects. Lead the overall desig

We are seeking experienced laboratory professionals to join the Project Services team at IQVIA Laboratories.This role is 100% remote (Eastern Time business hours). We are hiring at multiple levels candidates are aligned to the appropriate level based on experience.We hire passionate

We are seeking experienced laboratory professionals to join the Project Services team at IQVIA Laboratories.This role is 100% remote (Eastern Time business hours). We are hiring at multiple levels candidates are aligned to the appropriate level based on experience.We hire passionate

Title: Attorney 1Overview:IQVIA is seeking a mid-level attorney to join our corporate in-house team. The Attorney 1 will report directly to the Assistant General Counsel Securities and work closely with our Finance Treasury Investor Relations and Sustainability teams to prepare SEC fi

Title: Attorney 1Overview:IQVIA is seeking a mid-level attorney to join our corporate in-house team. The Attorney 1 will report directly to the Assistant General Counsel Securities and work closely with our Finance Treasury Investor Relations and Sustainability teams to prepare SEC fi

Job OverviewIQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure collaborative culture and deep therapeutic expertise allow us to deliver tailored solutions that help b

Job OverviewIQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure collaborative culture and deep therapeutic expertise allow us to deliver tailored solutions that help b

Job OverviewThe TMF Specialist serves as the liaison between Records Management and user departments regarding Trial Master files. Apply Records Management expertise to provide project related assistance across complex and multiple project(s) sites and project teams. Ensure all work i

Job OverviewThe TMF Specialist serves as the liaison between Records Management and user departments regarding Trial Master files. Apply Records Management expertise to provide project related assistance across complex and multiple project(s) sites and project teams. Ensure all work i

Sr. Product ManagerMeasurement Studies Platforms & Data ServicesIQVIA DigitalLocation: RemoteJob Type: Full-timeIQVIA Digital Overview:IQVIA Digital powers exceptional brand experiences delivering innovative solutions based on a customer-first insights-driven and integrated omnichanne

Sr. Product ManagerMeasurement Studies Platforms & Data ServicesIQVIA DigitalLocation: RemoteJob Type: Full-timeIQVIA Digital Overview:IQVIA Digital powers exceptional brand experiences delivering innovative solutions based on a customer-first insights-driven and integrated omnichanne