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Provide medical expertise on pharmacovigilance services to divisions as requested. The Associate Medical Safety Director participates in all aspects of Medical Safetys involvement on assigned trials and stand alone safety projects with appropriate oversight from management or more sen

Provide medical expertise on pharmacovigilance services to divisions as requested. The Associate Medical Safety Director participates in all aspects of Medical Safetys involvement on assigned trials and stand alone safety projects with appropriate oversight from management or more sen

IQVIA is currently recruiting for an Associate Consultant within the Primary Intelligence team. The successful candidate will have the opportunity to work with experienced healthcare consultants on integrated research solutioning to deliver comprehensive market insights to our clients

IQVIA is currently recruiting for an Associate Consultant within the Primary Intelligence team. The successful candidate will have the opportunity to work with experienced healthcare consultants on integrated research solutioning to deliver comprehensive market insights to our clients

Job OverviewThis is a senior role on our Global Business Operations team. It will be responsible for providing strategy input for proposals & budgets for one of IQVIAs specialist areas.This is a fully remote role although we do have offices in South Africa Bulgaria Romania Slovakia an

Job OverviewThis is a senior role on our Global Business Operations team. It will be responsible for providing strategy input for proposals & budgets for one of IQVIAs specialist areas.This is a fully remote role although we do have offices in South Africa Bulgaria Romania Slovakia an

Job Description SummaryJob OverviewPerform analysis and reporting of Phase I-IV clinical pharmacology studies such as dose tolerance dose proportionality mass balance concept testing bioavailability thorough QTc drug-drug interactions and special population (age effects renal disease

Job Description SummaryJob OverviewPerform analysis and reporting of Phase I-IV clinical pharmacology studies such as dose tolerance dose proportionality mass balance concept testing bioavailability thorough QTc drug-drug interactions and special population (age effects renal disease

Internal Medical Translator/In-house Linguist (Korean to English)Location: EMEA - Home-BasedUnlock Your Potential with IQVIA Language Solutions!At IQVIA Language Solutions we stand out as the only 100% language solutions provider dedicated to transforming the way the life sciences ind

Internal Medical Translator/In-house Linguist (Korean to English)Location: EMEA - Home-BasedUnlock Your Potential with IQVIA Language Solutions!At IQVIA Language Solutions we stand out as the only 100% language solutions provider dedicated to transforming the way the life sciences ind

Job OverviewThe Associate Medical Director will provide medical clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned trials. Serve as a medical expert during project delivery lifecycle. Pr

Job OverviewThe Associate Medical Director will provide medical clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned trials. Serve as a medical expert during project delivery lifecycle. Pr

IQVIA is a leading global provider of advanced analytics technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a health

IQVIA is a leading global provider of advanced analytics technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a health

The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall pharmacovigilance process and determine the medical and scientific relevance of serious adverse event reports within the context of the prod

The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall pharmacovigilance process and determine the medical and scientific relevance of serious adverse event reports within the context of the prod

IQVIA is a leading global provider of advanced analytics technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a health

IQVIA is a leading global provider of advanced analytics technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a health

Job OverviewPerform manage and co-ordinate activities for assigned opportunities/ projects. Perform data mining and analysis formulate recommendations and present to internal and potentially external stakeholders. Train and support new team members / junior staff. Make recommendations

Job OverviewPerform manage and co-ordinate activities for assigned opportunities/ projects. Perform data mining and analysis formulate recommendations and present to internal and potentially external stakeholders. Train and support new team members / junior staff. Make recommendations

Q2 Solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure enterprise-wide biospecimen and consent management solutions. With a relentless focus on quality and innovation Q2 Solutions uses its global experience and scientif

Q2 Solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure enterprise-wide biospecimen and consent management solutions. With a relentless focus on quality and innovation Q2 Solutions uses its global experience and scientif

Job Overview.Direct and manage the execution of the strategic operational and financial delivery of required Site Activation activities including but not limited to Site ID and Selection Ethics and Regulatory processes and Site Contracting for assigned studies as determined by Company

Job Overview.Direct and manage the execution of the strategic operational and financial delivery of required Site Activation activities including but not limited to Site ID and Selection Ethics and Regulatory processes and Site Contracting for assigned studies as determined by Company

The IQVIA Sponsor-Dedicated Clinical Trials Assistant Team issupporting the project teams in the execution of clinical the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas. You will be involved i

The IQVIA Sponsor-Dedicated Clinical Trials Assistant Team issupporting the project teams in the execution of clinical the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas. You will be involved i

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

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

Senior HR Business Partner (Grade)Job OverviewThe Senior HR Business Partner is a strategic role responsible for implementing and executing HR policies and processes for assigned business units. This role requires a deep understanding of both technical and business aspects to effectiv

Senior HR Business Partner (Grade)Job OverviewThe Senior HR Business Partner is a strategic role responsible for implementing and executing HR policies and processes for assigned business units. This role requires a deep understanding of both technical and business aspects to effectiv

Job OverviewProvide oversight and leadership to Senior Global Trial managers (SGTMs) for project productivity delivery and quality resulting in strong financial performance and customer satisfaction. Work with Clinical teams to focus on leveraging deep therapeutic expertise and IQVIA

Job OverviewProvide oversight and leadership to Senior Global Trial managers (SGTMs) for project productivity delivery and quality resulting in strong financial performance and customer satisfaction. Work with Clinical teams to focus on leveraging deep therapeutic expertise and IQVIA

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 Functions Manage staff in accordance with organizations policies and applicable regulati

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 Functions Manage staff in accordance with organizations policies and applicable regulati

Every 30 minutes a stroke patient who could have been saved either dies or is permanently disabled because they were treated in the wrong hospital.Our mission is clear: to increase the number of patients treated in stroke-ready hospitals and to optimize the quality of treatment in all

Every 30 minutes a stroke patient who could have been saved either dies or is permanently disabled because they were treated in the wrong hospital.Our mission is clear: to increase the number of patients treated in stroke-ready hospitals and to optimize the quality of treatment in all

Job OverviewReview assess and process Safety data and information across service lines received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and internal guide

Job OverviewReview assess and process Safety data and information across service lines received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and internal guide