IQVIA

Senior Product Owner (Product Strategy Data & Integration)IQVIA is seeking a Senior Product responsible for driving strategic initiatives that advance IQVIAs technology ecosystem for the scoring and analytics of Clinical Outcome Assessments (COAs) digital measures and composite measur

Senior Product Owner (Product Strategy Data & Integration)IQVIA is seeking a Senior Product responsible for driving strategic initiatives that advance IQVIAs technology ecosystem for the scoring and analytics of Clinical Outcome Assessments (COAs) digital measures and composite measur

Job OverviewDesigns/develops software solutions and business process solutions based on business needs and requirements using specialized domain knowledge and developed business expertise.Focuses on software quality standards for all aspects of work; establishes advanced software test

Job OverviewDesigns/develops software solutions and business process solutions based on business needs and requirements using specialized domain knowledge and developed business expertise.Focuses on software quality standards for all aspects of work; establishes advanced software test

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

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 OverviewThe Medical Director for the Hematology-Oncology Center of Excellence provides strategic medical and scientific subject matter input to IQVIA in this therapeutic area informed by their training experience and expertise. The activity of the medical director includes but is

Job OverviewThe Medical Director for the Hematology-Oncology Center of Excellence provides strategic medical and scientific subject matter input to IQVIA in this therapeutic area informed by their training experience and expertise. The activity of the medical director includes but is

Primary Function:Centralized Monitoring Lead(CML) partners with the Clinical Lead and local country Site Monitors in project execution. Provides centralized support to monitoring visits and site management for a variety of protocols sites and therapeutic areas. Monitors study start-up

Primary Function:Centralized Monitoring Lead(CML) partners with the Clinical Lead and local country Site Monitors in project execution. Provides centralized support to monitoring visits and site management for a variety of protocols sites and therapeutic areas. Monitors study start-up

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

The TeamIQVIA is a fast-growing and highly successful consultancy business focusing on delivering tangible business results to our clients who are key decision-makers and business managers across the international pharmaceutical and healthcare industry. With direct access to the world

The TeamIQVIA is a fast-growing and highly successful consultancy business focusing on delivering tangible business results to our clients who are key decision-makers and business managers across the international pharmaceutical and healthcare industry. With direct access to the world

Job OverviewProvide strategic leadership at customer account level for multiple large projects as assigned by senior management team. Act as Sponsors primary point of contact throughout project duration for local and globally scoped deliverables (programs) with single/multiple Lifecyc

Job OverviewProvide strategic leadership at customer account level for multiple large projects as assigned by senior management team. Act as Sponsors primary point of contact throughout project duration for local and globally scoped deliverables (programs) with single/multiple Lifecyc

IQVIA is The Human Data Science Company focused on using data and science to help healthcare clients find better solutions for their patients. IQVIA offers a broad range of solutions that harness advances in healthcare information technologyanalyticsand human ingenuity to drive health

IQVIA is The Human Data Science Company focused on using data and science to help healthcare clients find better solutions for their patients. IQVIA offers a broad range of solutions that harness advances in healthcare information technologyanalyticsand human ingenuity to drive health

Join Our Team as a Therapeutic Strategy Lead!Are you passionate about creating innovative delivery strategies that meet customer needs Do you thrive in a collaborative environment where you can make a real impact If so we have the perfect opportunity for you!PurposeAs a Therapeutic St

Join Our Team as a Therapeutic Strategy Lead!Are you passionate about creating innovative delivery strategies that meet customer needs Do you thrive in a collaborative environment where you can make a real impact If so we have the perfect opportunity for you!PurposeAs a Therapeutic St

Internal Job DescriptionThis position is not eligible for employment visa sponsorship now or in the future. Applicants must be legally authorized to work in the country of employment without the need for current or future employer sponsorship.Job Profile SummarySupports the delivery o

Internal Job DescriptionThis position is not eligible for employment visa sponsorship now or in the future. Applicants must be legally authorized to work in the country of employment without the need for current or future employer sponsorship.Job Profile SummarySupports the delivery o

Regulatory Affairs IVDR - Contractor (North Africa)Location: Algeria Morocco or Tunisia (Remote/Hybrid as applicable)Contract Type: ContractorAbout the OpportunityWe are seeking an experienced Regulatory Affairs IVDR Contractor to support regulatory activities across the EMEA region w

Regulatory Affairs IVDR - Contractor (North Africa)Location: Algeria Morocco or Tunisia (Remote/Hybrid as applicable)Contract Type: ContractorAbout the OpportunityWe are seeking an experienced Regulatory Affairs IVDR Contractor to support regulatory activities across the EMEA region w

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

Clinical Research Coordinator in YorkWorking Hours: 24 hours per weekStart Date: ImmediatelyDuration: Approximately 6 monthsIQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in York. This part-time position offers a unique oppo

Clinical Research Coordinator in YorkWorking Hours: 24 hours per weekStart Date: ImmediatelyDuration: Approximately 6 monthsIQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in York. This part-time position offers a unique oppo

We are looking for a new team member to join in our Regulatory Offering Management Team the development enhancement and launch of Regulatory Intelligence solutions for the pharmaceutical industry. This role will work closely with cross-functional and international teams to drive offer

We are looking for a new team member to join in our Regulatory Offering Management Team the development enhancement and launch of Regulatory Intelligence solutions for the pharmaceutical industry. This role will work closely with cross-functional and international teams to drive offer

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

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

Job OverviewAs Database Management Analyst your primary responsibilities are:-Read Understand and program Medidata Rave Edit checks and custom function (C# Programming) from Data validation specification which meets Client requirementGood working understanding of EDC. Qualifications B

Job OverviewAs Database Management Analyst your primary responsibilities are:-Read Understand and program Medidata Rave Edit checks and custom function (C# Programming) from Data validation specification which meets Client requirementGood working understanding of EDC. Qualifications B

Join our team as a Site Enrollment and Engagement Lead and play a pivotal role in advancing clinical research. This role collaborates with research staff and stakeholders to drive trial recruitment and deliver study-specific training. Acting as a strategic partner you will optimize si

Join our team as a Site Enrollment and Engagement Lead and play a pivotal role in advancing clinical research. This role collaborates with research staff and stakeholders to drive trial recruitment and deliver study-specific training. Acting as a strategic partner you will optimize si