IQVIA

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.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Sta

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.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Sta

On behalf of our Client a global pharmaceutical company IQVIA is looking for a Key Account Manager who can join an exciting working environment in a dynamic atmosphere areas in the therapeutic area of oncology. WORKING AREA:Centre of ItalyMAIN TASKS AND RESPONSABILITIES:Achieve territ

On behalf of our Client a global pharmaceutical company IQVIA is looking for a Key Account Manager who can join an exciting working environment in a dynamic atmosphere areas in the therapeutic area of oncology. WORKING AREA:Centre of ItalyMAIN TASKS AND RESPONSABILITIES:Achieve territ

IQVIA is recruiting for a Sales Specialist DevonIn this role you will be responsible for developing sales in strategic accounts across Devon (Derriford/ Plymouth and Torbay). In this role you will become an integral part of the sales team supported by several clinical specialists in

IQVIA is recruiting for a Sales Specialist DevonIn this role you will be responsible for developing sales in strategic accounts across Devon (Derriford/ Plymouth and Torbay). In this role you will become an integral part of the sales team supported by several clinical specialists in

We are currently looking for an intern to join our Health Economics team in Milan.As an intern with IQVIA you will actively participate in/support the development and delivery of Health Economics studies to help pharmaceutical companies communicate the value of their innovations to st

We are currently looking for an intern to join our Health Economics team in Milan.As an intern with IQVIA you will actively participate in/support the development and delivery of Health Economics studies to help pharmaceutical companies communicate the value of their innovations to st

Clinical Specialist Consultant - HungarianLocation: Remote/virtualHours: Estimated 2-8h/weekRole: Clinical SpecialistJob Description:The Clinical Specialist reviews scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardized manne

Clinical Specialist Consultant - HungarianLocation: Remote/virtualHours: Estimated 2-8h/weekRole: Clinical SpecialistJob Description:The Clinical Specialist reviews scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardized manne

Job Description SummaryWorking with the wider Project Management team the Junior Translation Project Manager is responsible for coordinating and managing the full lifecycle of translation and localization projects to completion whilst ensuring IQVIAs standards are met. Manage multiple

Job Description SummaryWorking with the wider Project Management team the Junior Translation Project Manager is responsible for coordinating and managing the full lifecycle of translation and localization projects to completion whilst ensuring IQVIAs standards are met. Manage multiple

Clinical Specialist Consultant - Indonesian SpeakingLocation: Remote/virtualHours: Estimated 10-16h/monthRole: Clinical SpecialistJob Description:The Clinical Specialist reviews scales administered by raters in a clinical trial to ensure that assessments are being conducted in a stand

Clinical Specialist Consultant - Indonesian SpeakingLocation: Remote/virtualHours: Estimated 10-16h/monthRole: Clinical SpecialistJob Description:The Clinical Specialist reviews scales administered by raters in a clinical trial to ensure that assessments are being conducted in a stand

Are you looking for an opportunity to work with an industry-leading company IQVIA is currently recruiting for a Site Research Assistant to support a site in Gandrup Denmark.This role with an immediate start is for 8 hours per week and is expected to last around seven months.The succes

Are you looking for an opportunity to work with an industry-leading company IQVIA is currently recruiting for a Site Research Assistant to support a site in Gandrup Denmark.This role with an immediate start is for 8 hours per week and is expected to last around seven months.The succes

Clinical Specialist Consultant - Malay SpeakingLocation: Remote/virtualHours: Estimated 10-16h/monthRole: Clinical SpecialistJob Description:The Clinical Specialist reviews scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardiz

Clinical Specialist Consultant - Malay SpeakingLocation: Remote/virtualHours: Estimated 10-16h/monthRole: Clinical SpecialistJob Description:The Clinical Specialist reviews scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardiz

Account Director PurplemoonAbout Us:Purplemoon an IQVIA Company is a leading full-service marketing agency specializing in healthcare and pharmaceutical marketing and training with a specific focus on rare disease. Our Client Services team leads the agency to act as the strategic liai

Account Director PurplemoonAbout Us:Purplemoon an IQVIA Company is a leading full-service marketing agency specializing in healthcare and pharmaceutical marketing and training with a specific focus on rare disease. Our Client Services team leads the agency to act as the strategic liai

Medical Devices Sales SpecialistIQVIA are currently recruiting for a Medical Devices Sales Specialist to join the team in Dublin.In this role you will manage your territory as if it is your own business maintaining key customers and core business. You will be responsible for developin

Medical Devices Sales SpecialistIQVIA are currently recruiting for a Medical Devices Sales Specialist to join the team in Dublin.In this role you will manage your territory as if it is your own business maintaining key customers and core business. You will be responsible for developin

Job OverviewProvide advanced technical expertise to develop and maintain programs to meet internal and external clients needs. Plan and lead the development of project-related solutions to the full scope of statistical programming tasks. Provide technical expertise to the Statistical

Job OverviewProvide advanced technical expertise to develop and maintain programs to meet internal and external clients needs. Plan and lead the development of project-related solutions to the full scope of statistical programming tasks. Provide technical expertise to the Statistical

Currently seeking Senior Clinical Research Associate for our FSP team Step into a dynamic role where youll drive innovation and excellence in clinical research. As a key player in our team youll ensure that study sites are not just compliant but thriving contributing to groundbreaking

Currently seeking Senior Clinical Research Associate for our FSP team Step into a dynamic role where youll drive innovation and excellence in clinical research. As a key player in our team youll ensure that study sites are not just compliant but thriving contributing to groundbreaking

Job OverviewDirect and manage the delivery of all required site activation maintenance and regulatory activities for selected studies or multi-protocol programs including pre-award activities oversight of the scope of work budget and resources.This role requires a candidate strong in

Job OverviewDirect and manage the delivery of all required site activation maintenance and regulatory activities for selected studies or multi-protocol programs including pre-award activities oversight of the scope of work budget and resources.This role requires a candidate strong in

1. 为研究中心提供实际支持最大限度地提高患者入组率2. 与研究中心合作确定并解决患者招募中存在的困难确定常见的问题并与申办方和利益相关方合作提出有建设性的意见以克服入组障碍3.不定期向研究团队提供有关临床研究中入排除标准的相关培训必要时为新加入的研究人员进行培训4. 为临床研究中心的医疗人员提供资源分享患者识别及防止脱落的最佳做法和策略5. 通过现场确定患者筛选流程及入组途径与相关科室合作提升研究中心对方案的认识以增加患者入组的潜力6. 作为临床研究的联络人高效解决相关问题 (就相应试验事宜向申办方临床研究管理人员及CRO/ ARO提供反馈)7. 向项目管理团队

1. 为研究中心提供实际支持最大限度地提高患者入组率2. 与研究中心合作确定并解决患者招募中存在的困难确定常见的问题并与申办方和利益相关方合作提出有建设性的意见以克服入组障碍3.不定期向研究团队提供有关临床研究中入排除标准的相关培训必要时为新加入的研究人员进行培训4. 为临床研究中心的医疗人员提供资源分享患者识别及防止脱落的最佳做法和策略5. 通过现场确定患者筛选流程及入组途径与相关科室合作提升研究中心对方案的认识以增加患者入组的潜力6. 作为临床研究的联络人高效解决相关问题 (就相应试验事宜向申办方临床研究管理人员及CRO/ ARO提供反馈)7. 向项目管理团队

Only EU Citizens are eligible to apply for this position.Proficiency in PythonJob OverviewWe are seeking a Data Engineer to design build and maintain robust data solutions that enable efficient data processing and analytics. The role involves developing scalable data pipelines integra

Only EU Citizens are eligible to apply for this position.Proficiency in PythonJob OverviewWe are seeking a Data Engineer to design build and maintain robust data solutions that enable efficient data processing and analytics. The role involves developing scalable data pipelines integra

Clinical Specialist / Stroke Rater Kannada SpeakingLocation: RemoteHours: Estimated 212 hours per month flexibleRole OverviewThe Clinical Specialist supports stroke clinical trials by administering standardized assessments and ensuring data quality and consistency. This includes rati

Clinical Specialist / Stroke Rater Kannada SpeakingLocation: RemoteHours: Estimated 212 hours per month flexibleRole OverviewThe Clinical Specialist supports stroke clinical trials by administering standardized assessments and ensuring data quality and consistency. This includes rati

Clinical Specialist / Stroke Rater - Telugu SpeakingLocation: RemoteHours: Estimated 212 hours per month flexibleRole OverviewThe Clinical Specialist supports stroke clinical trials by administering standardized assessments and ensuring data quality and consistency. This includes rati

Clinical Specialist / Stroke Rater - Telugu SpeakingLocation: RemoteHours: Estimated 212 hours per month flexibleRole OverviewThe Clinical Specialist supports stroke clinical trials by administering standardized assessments and ensuring data quality and consistency. This includes rati

The flex resource performing the Program Delivery Management IP services will be responsible for the oversight and the training strategy/delivery of Investigational Product (IP) across relevant GCO roles and sites. Activities include engaging with investigational sites as it relates t

The flex resource performing the Program Delivery Management IP services will be responsible for the oversight and the training strategy/delivery of Investigational Product (IP) across relevant GCO roles and sites. Activities include engaging with investigational sites as it relates t

This role is a 12 months contract role please apply if you are comfortable with the duration.Project Leads are an integral part of clinical trial delivery liaising withclinical teams to improve patients lives by bringing new drugs to the market faster. The Project Lead is an essential

This role is a 12 months contract role please apply if you are comfortable with the duration.Project Leads are an integral part of clinical trial delivery liaising withclinical teams to improve patients lives by bringing new drugs to the market faster. The Project Lead is an essential