IQVIA

Intern EMEA Life Sciences Strategy ConsultingIQVIA is The Human Data Science Company combining data technology advanced analytics and human expertise to help healthcare clients improve outcomes for patients. Our solutions support better decision-making across the healthcare ecosystem

Intern EMEA Life Sciences Strategy ConsultingIQVIA is The Human Data Science Company combining data technology advanced analytics and human expertise to help healthcare clients improve outcomes for patients. Our solutions support better decision-making across the healthcare ecosystem

Key Account Manager Primary & Secondary CareLocation: Surrey & HampshireWe are partnering with a leading healthcare organisation to recruit aKey Account Managerto support the launch and growth of afirstinclass nonhormonal therapywithin womens health. This is ahighimpact fieldbased ro

Key Account Manager Primary & Secondary CareLocation: Surrey & HampshireWe are partnering with a leading healthcare organisation to recruit aKey Account Managerto support the launch and growth of afirstinclass nonhormonal therapywithin womens health. This is ahighimpact fieldbased ro

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通过日语N2检定或具备同等程度日语能力并通过大学英语CET4级或以上学历要求为本科及以上日语专业可如具备生物医药相关背景可优先考虑能够保证每周至少出勤24-32小时实习地点大连办公室大连市高新园区腾飞软件园一期西翼10楼*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offe

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通过日语N2检定或具备同等程度日语能力并通过大学英语CET4级或以上学历要求为本科及以上日语专业可如具备生物医药相关背景可优先考虑能够保证每周至少出勤24-32小时实习地点大连办公室大连市高新园区腾飞软件园一期西翼10楼*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offe

Essential Functions Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP) protocol) customer requirements (contract) and internal requirements (policies Standard Operating

Essential Functions Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP) protocol) customer requirements (contract) and internal requirements (policies Standard Operating

Job OverviewIndependently manage end-to-end delivery of dataproducts and platformsfor single/multi-service projects ensuring quality deliverables on time and within budget to customer satisfaction. Provide comprehensive data managementexpertisetoClinicalData Management (CDM) team to p

Job OverviewIndependently manage end-to-end delivery of dataproducts and platformsfor single/multi-service projects ensuring quality deliverables on time and within budget to customer satisfaction. Provide comprehensive data managementexpertisetoClinicalData Management (CDM) team to p

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

Buscamos un delegado de farmacia para realizar funciones de sell out.Tu trabajo consistirá en promocionar varios productos en las farmacias asignadas dentro de tu zona de trabajo contribuyendo así al plan de negocio nacional.El puesto requerirá que adoptes un enfoque amplio del negoci

Buscamos un delegado de farmacia para realizar funciones de sell out.Tu trabajo consistirá en promocionar varios productos en las farmacias asignadas dentro de tu zona de trabajo contribuyendo así al plan de negocio nacional.El puesto requerirá que adoptes un enfoque amplio del negoci

Base level rolePerform comprehensive data management tasks including data review query generation and query resolution. This may also include but is not limited to creation of eCRF completion guidelines entry of test data for eCRF and the Data Review Model testing of data validation r

Base level rolePerform comprehensive data management tasks including data review query generation and query resolution. This may also include but is not limited to creation of eCRF completion guidelines entry of test data for eCRF and the Data Review Model testing of data validation r

Clinical Research Associate Your responsibilities will include:Performing site selection initiation monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements

Clinical Research Associate Your responsibilities will include:Performing site selection initiation monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements

Job OverviewThe Sr Clinical Research Associate (CRA) is responsible for performing highquality monitoring activities and site management to ensure that clinical sites conduct studies in full compliance with the protocol ICHGCP guidelines regulatory requirements and sponsor expectation

Job OverviewThe Sr Clinical Research Associate (CRA) is responsible for performing highquality monitoring activities and site management to ensure that clinical sites conduct studies in full compliance with the protocol ICHGCP guidelines regulatory requirements and sponsor expectation

This Role is based in Jeddah.Contract Duration - 1 year.Position Overview:We are looking for a highly organized and proactive Event Logistics and Governance Coordinator to handle the planning execution and management of events logistics and governance processes.The ideal candidate wil

This Role is based in Jeddah.Contract Duration - 1 year.Position Overview:We are looking for a highly organized and proactive Event Logistics and Governance Coordinator to handle the planning execution and management of events logistics and governance processes.The ideal candidate wil

Bio-Rep AssociateIQIVIA Laboratories Office-based and hybrid options availableIQVIA Laboratories is a global leader in drug discovery and development offering comprehensive central and specialty biomarker services. Our expertise includes genomics immunoassays flow cytometry anatomic p

Bio-Rep AssociateIQIVIA Laboratories Office-based and hybrid options availableIQVIA Laboratories is a global leader in drug discovery and development offering comprehensive central and specialty biomarker services. Our expertise includes genomics immunoassays flow cytometry anatomic p

Junior Reporting AnalystChesterfield UKOffice basedWe are looking for a motivated and detailoriented individual to join our Reporting Function as a Junior Reporting Analyst. This is an excellent opportunity for someone early in their career who enjoys working with data and wants to de

Junior Reporting AnalystChesterfield UKOffice basedWe are looking for a motivated and detailoriented individual to join our Reporting Function as a Junior Reporting Analyst. This is an excellent opportunity for someone early in their career who enjoys working with data and wants to de

Territory Area: Leicester / Nottingham / LincolnDo you want to join a company that nurtures its employees and advocates for an employee work-life balance Do you have excellent sales experience and wish to join a company that has led the way in the development manufacture and marketing

Territory Area: Leicester / Nottingham / LincolnDo you want to join a company that nurtures its employees and advocates for an employee work-life balance Do you have excellent sales experience and wish to join a company that has led the way in the development manufacture and marketing

Job OverviewProject Leads are an integral part of clinical trial delivery liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical st

Job OverviewProject Leads are an integral part of clinical trial delivery liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical st

Location:Brazil (Sao Paulo) About Us:Join our team and help shape the future of our organization. We are a leading company committed to excellence and innovation seeking a talented Senior Recruiter to support our growth.Job Overview: Supervises a small team of site activation support

Location:Brazil (Sao Paulo) About Us:Join our team and help shape the future of our organization. We are a leading company committed to excellence and innovation seeking a talented Senior Recruiter to support our growth.Job Overview: Supervises a small team of site activation support

Job OverviewPerform 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.Please note for this role you must be based in the Netherlands. Essential Functions A

Job OverviewPerform 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.Please note for this role you must be based in the Netherlands. Essential Functions A

Essential FunctionsDevelop Coordinate the development of investigator grants and estimates contracting strategies and proposal text to support the proposal development process.Develop contract language payment language and budget templates as required as applicable to the positionUtil

Essential FunctionsDevelop Coordinate the development of investigator grants and estimates contracting strategies and proposal text to support the proposal development process.Develop contract language payment language and budget templates as required as applicable to the positionUtil

Project Role: Data Strategist or Data Acquisition ExpertWork Experience: 5 to10 YearsWork location: Anywhere in IndiaWork Mode: RemoteMust Have Skills: Data Acquistion data transfer handling blinded data quality assessments.Job Overview: Plan and coordinate database design developmen

Project Role: Data Strategist or Data Acquisition ExpertWork Experience: 5 to10 YearsWork location: Anywhere in IndiaWork Mode: RemoteMust Have Skills: Data Acquistion data transfer handling blinded data quality assessments.Job Overview: Plan and coordinate database design developmen

Job OverviewCTEs collaborate with research staff and other stakeholders to drive trial recruitment and to support study specific training needs. The CTE acts as a strategic partner to both external and internal stakeholders to optimise the site experience and performance. Leads the re

Job OverviewCTEs collaborate with research staff and other stakeholders to drive trial recruitment and to support study specific training needs. The CTE acts as a strategic partner to both external and internal stakeholders to optimise the site experience and performance. Leads the re