IQVIA

Join IQVIA as a SrCRA II/III (m/w/d) in our Clinical Site Management department home-based throughout Germany. You will focus on a comprehensive clinical trial management in a variety of indications and learn about the diverse scientific approach of the sponsors. Beside establishing s

Join IQVIA as a SrCRA II/III (m/w/d) in our Clinical Site Management department home-based throughout Germany. You will focus on a comprehensive clinical trial management in a variety of indications and learn about the diverse scientific approach of the sponsors. Beside establishing s

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 adv

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 adv

Job OverviewManage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and meeting project objectives.Essential FunctionsManage staff in accordance with organizations policies and applicable regulatio

Job OverviewManage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and meeting project objectives.Essential FunctionsManage staff in accordance with organizations policies and applicable regulatio

Job OverviewSecure and retain business through professional consultative proactive sales activities directed at decision-makers and decision influencers at existing and new pharmaceutical and healthcare clients.Support the growth of IQVIAs Real World Evidence (RWE) business in LATAM w

Job OverviewSecure and retain business through professional consultative proactive sales activities directed at decision-makers and decision influencers at existing and new pharmaceutical and healthcare clients.Support the growth of IQVIAs Real World Evidence (RWE) business in LATAM w

Job DescriptionProduction of High-Quality Deliverables: Completes and reviews more complex assigned tasks with a focus on accuracy. Conducts all appropriate validation requirements according to Standard Operating Procedures (SOPs) for each task undertaken. Checks programming logs for

Job DescriptionProduction of High-Quality Deliverables: Completes and reviews more complex assigned tasks with a focus on accuracy. Conducts all appropriate validation requirements according to Standard Operating Procedures (SOPs) for each task undertaken. Checks programming logs for

Job OverviewPerform/Assist the Data Manager in managing various data management projects as per sponsor requirements and to provide efficient quality management products. Support coordinate with other departments sites and sponsors as and when necessaryEssential Functions Perform/Assi

Job OverviewPerform/Assist the Data Manager in managing various data management projects as per sponsor requirements and to provide efficient quality management products. Support coordinate with other departments sites and sponsors as and when necessaryEssential Functions Perform/Assi

Provide support to management in the promotion and assessment of compliance with regulations guidelines and operating procedures. Manage the quality assurance oversight of projects assignments training and staff. Conduct independent audits to assess compliance with regulations guideli

Provide support to management in the promotion and assessment of compliance with regulations guidelines and operating procedures. Manage the quality assurance oversight of projects assignments training and staff. Conduct independent audits to assess compliance with regulations guideli

Position SummaryThe Database Operator (DBO) is responsible for maintaining and enhancing IQVIAs healthcare reference databases including Healthcare Professionals (HCPs) Healthcare Organizations (HCOs) and related healthcare entities. The role requires conducting detailed research vali

Position SummaryThe Database Operator (DBO) is responsible for maintaining and enhancing IQVIAs healthcare reference databases including Healthcare Professionals (HCPs) Healthcare Organizations (HCOs) and related healthcare entities. The role requires conducting detailed research vali

根据试验方案合同规定的工作范围SOP和GCP的要求进行研究中心筛选启动监查和关闭访视 可同时负责多个方案研究中心和治疗领域内的研究中心监查工作 对所负责的研究中心进行方案和研究相关的培训与研究中心进行定期沟通以管理项目进行中的要求和问题 评估研究中心工作的质量和完整性确定研究中心是否是按照方案和适用的法规进行研究将质量问题汇报给负责的PM和/或直线经理 通过追踪注册申报和批复招募和入选病例报告表CRF完成和递交以及数据疑问产生和解决的情况管理所负责研究中心的进展创建和维护与研究中心管理监查访视的发现以及行动计划相关的文件递交访视报告和其他所需研究文件 负责相应研究

根据试验方案合同规定的工作范围SOP和GCP的要求进行研究中心筛选启动监查和关闭访视 可同时负责多个方案研究中心和治疗领域内的研究中心监查工作 对所负责的研究中心进行方案和研究相关的培训与研究中心进行定期沟通以管理项目进行中的要求和问题 评估研究中心工作的质量和完整性确定研究中心是否是按照方案和适用的法规进行研究将质量问题汇报给负责的PM和/或直线经理 通过追踪注册申报和批复招募和入选病例报告表CRF完成和递交以及数据疑问产生和解决的情况管理所负责研究中心的进展创建和维护与研究中心管理监查访视的发现以及行动计划相关的文件递交访视报告和其他所需研究文件 负责相应研究

single/multi-service projects with minimal guidance ensuring quality deliverables on time and within budget to customer satisfaction. Provide comprehensive data management expertise to Data Management (DM) team to provide high quality data management products that meet customer needs.

single/multi-service projects with minimal guidance ensuring quality deliverables on time and within budget to customer satisfaction. Provide comprehensive data management expertise to Data Management (DM) team to provide high quality data management products that meet customer needs.

职位概要 作为研究中心研究者团队的成员在研究中心遵照研究方案商定的工作范围GCP申办者/公 司SOP及其他相关指南和法规的要求来协调和执行所分配的临床试验职责 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和其他协调工作 在

职位概要 作为研究中心研究者团队的成员在研究中心遵照研究方案商定的工作范围GCP申办者/公 司SOP及其他相关指南和法规的要求来协调和执行所分配的临床试验职责 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和其他协调工作 在

Job OverviewProvides high quality timely development and on-time input to solutions for service delivery managed services or implementation oriented client projects. Assignments range in complexity from basic analysis and problem solving to assisting in the development of more complex

Job OverviewProvides high quality timely development and on-time input to solutions for service delivery managed services or implementation oriented client projects. Assignments range in complexity from basic analysis and problem solving to assisting in the development of more complex

Job OverviewPerform 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 (sele

Job OverviewPerform 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 (sele

职责 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和其他协调工作 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 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 协助研究者归档研究资料并提交至伦理委员会或其他权威

职责 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和其他协调工作 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 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 协助研究者归档研究资料并提交至伦理委员会或其他权威

IQVIA The Human Data Science Company is a leading global provider of advanced analytics technology solutions and clinical research services to the life sciences and healthcare industries. Our mission is to create intelligent connections that deliver unique innovations and actionable

IQVIA The Human Data Science Company is a leading global provider of advanced analytics technology solutions and clinical research services to the life sciences and healthcare industries. Our mission is to create intelligent connections that deliver unique innovations and actionable

Solution Specialist Clinical eSource PlatformLocation:Sydney or MelbourneExperience Required:5 yearsWe are seeking a Solution Specialistto serve as a SaaS implementation and support expert for IQVIAs Clinical eSource this role you will partner with early-phase CROs and Sponsors to d

Solution Specialist Clinical eSource PlatformLocation:Sydney or MelbourneExperience Required:5 yearsWe are seeking a Solution Specialistto serve as a SaaS implementation and support expert for IQVIAs Clinical eSource this role you will partner with early-phase CROs and Sponsors to d

Site Enrolment & Engagement Lead12-month fixed term contract. Open to all locations across Australia.About the roleWe are looking for a Site Enrolment & Engagement Leadto support clinical research sites with patient recruitment retention and study-specific education. This is an excell

Site Enrolment & Engagement Lead12-month fixed term contract. Open to all locations across Australia.About the roleWe are looking for a Site Enrolment & Engagement Leadto support clinical research sites with patient recruitment retention and study-specific education. This is an excell

Job OverviewThe Assoc. Medical Director will be the medical expert on the IQVIA team working on a clinical research trial. This involves applying medical and scientific knowledge and expertise in support of the trial. These clinical trials will cover the full range of rheumatologic di

Job OverviewThe Assoc. Medical Director will be the medical expert on the IQVIA team working on a clinical research trial. This involves applying medical and scientific knowledge and expertise in support of the trial. These clinical trials will cover the full range of rheumatologic di

This is a home-based position open to candidates within the EMEA region.This service provides global coordination for the execution for unblinded/unmasked drug management including the general facilitation of the Unmasked Drug Oversight (UDO) process between the local Independent Drug

This is a home-based position open to candidates within the EMEA region.This service provides global coordination for the execution for unblinded/unmasked drug management including the general facilitation of the Unmasked Drug Oversight (UDO) process between the local Independent Drug

Internal Job DescriptionIQVIA is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients.Formed through the merger of IMS Health and Quintiles IQVIA offers a broad range of solutions that harness the pow

Internal Job DescriptionIQVIA is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients.Formed through the merger of IMS Health and Quintiles IQVIA offers a broad range of solutions that harness the pow