IQVIA

We are seeking Lab Technical Specialist to join IQVIA Laboratories at Buenos Aires Argentina.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose join us as we transform and acc

We are seeking Lab Technical Specialist to join IQVIA Laboratories at Buenos Aires Argentina.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose join us as we transform and acc

JOB SUMMARY:Responsible for medical data review and medical safety case processing and related safety activities. Performs review of medical data to ensure medical/scientific plausibility and to employ medical assessment and knowledge. Also provides medical expertise in assigned trial

JOB SUMMARY:Responsible for medical data review and medical safety case processing and related safety activities. Performs review of medical data to ensure medical/scientific plausibility and to employ medical assessment and knowledge. Also provides medical expertise in assigned trial

Clinical Trial Psych Rater - Portuguese SpeakingLocation: Remote/VirtualHours: Estimated 1016 hours per monthRole: Clinical SpecialistAbout IQVIAIQVIA is a global leader in advanced analytics technology solutions and clinical research services dedicated to driving healthcare forward.

Clinical Trial Psych Rater - Portuguese SpeakingLocation: Remote/VirtualHours: Estimated 1016 hours per monthRole: Clinical SpecialistAbout IQVIAIQVIA is a global leader in advanced analytics technology solutions and clinical research services dedicated to driving healthcare forward.

Job OverviewIQVIA is seeking an experienced and motivated Line Manager to lead and develop a team of clinical research professionals supporting the execution of clinical studies. This role is responsible for ensuring appropriate resource allocation employee development quality oversig

Job OverviewIQVIA is seeking an experienced and motivated Line Manager to lead and develop a team of clinical research professionals supporting the execution of clinical studies. This role is responsible for ensuring appropriate resource allocation employee development quality oversig

Job DescriptionTo fulfill this position you must be a passionate and enthusiastic person to grow the company business in the new technology and digital era. You are going to be responsible for enhancing the companys portfolio serving our clients throughout the Healthcare industry.Acco

Job DescriptionTo fulfill this position you must be a passionate and enthusiastic person to grow the company business in the new technology and digital era. You are going to be responsible for enhancing the companys portfolio serving our clients throughout the Healthcare industry.Acco

Job OverviewThe Senior HR Business Partner (HRBP) is a mature dynamic proactive and solutions-driven professional who plays a critical role in aligning HR strategies with business unit goals. This role bridges the global HR agenda with local business needs within the specified busines

Job OverviewThe Senior HR Business Partner (HRBP) is a mature dynamic proactive and solutions-driven professional who plays a critical role in aligning HR strategies with business unit goals. This role bridges the global HR agenda with local business needs within the specified busines

ResponsibilitiesLead all deliveries from loading bay log QC receipt in store and distribute as requiredManage and maintain stock on shelves in a tidy manner executing stock rotation on appropriate date orderOversee and record all stock movements and stock issues using Inventory contro

ResponsibilitiesLead all deliveries from loading bay log QC receipt in store and distribute as requiredManage and maintain stock on shelves in a tidy manner executing stock rotation on appropriate date orderOversee and record all stock movements and stock issues using Inventory contro

Clinical Trial Rater Borderline Personality Disorder (BPD)Location: Remote based in the USHours: Approximately 5h per weekRole: Clinical SpecialistStart: immediateContract based About IQVIAIQVIA is a global leader in advanced analytics technology solutions and clinical research servi

Clinical Trial Rater Borderline Personality Disorder (BPD)Location: Remote based in the USHours: Approximately 5h per weekRole: Clinical SpecialistStart: immediateContract based About IQVIAIQVIA is a global leader in advanced analytics technology solutions and clinical research servi

Clinical Research Coordinator Union SCWork Set-Up: On-siteSchedule Weekly Hours: 24 hours/weekAbout IQVIAIQVIA is a global leader in advanced analytics technology solutions and clinical research services dedicated to driving healthcare forward. We partner with the worlds leading pha

Clinical Research Coordinator Union SCWork Set-Up: On-siteSchedule Weekly Hours: 24 hours/weekAbout IQVIAIQVIA is a global leader in advanced analytics technology solutions and clinical research services dedicated to driving healthcare forward. We partner with the worlds leading pha

100% remote roleJob OverviewThe Medical Information Case Processor responsibilities include receiving and documenting incoming telephone calls or emails from investigative sites or other sources reporting Lifecycle Safety Data.This is a trilingual role requiring fluency in English Spa

100% remote roleJob OverviewThe Medical Information Case Processor responsibilities include receiving and documenting incoming telephone calls or emails from investigative sites or other sources reporting Lifecycle Safety Data.This is a trilingual role requiring fluency in English Spa

Job OverviewReview assess and process safety data and information across service lines received from various sources. Distribute reports/data to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and internal guidelines under

Job OverviewReview assess and process safety data and information across service lines received from various sources. Distribute reports/data to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and internal guidelines under

Clinical Trials Regulatory OfficerJob SummaryThe Clinical Trials Regulatory Officer prepares reviews and manages regulatory documentation to support clinical trial submissions in compliance with applicable regulatory requirements. The role provides regulatory support across clinical t

Clinical Trials Regulatory OfficerJob SummaryThe Clinical Trials Regulatory Officer prepares reviews and manages regulatory documentation to support clinical trial submissions in compliance with applicable regulatory requirements. The role provides regulatory support across clinical t

Associate Consultant and Statistician Statistics & Psychometrics Patient Centered SolutionsOverviewIQVIA provides scientific services spanning clinical trials real world evidence and consulting in all areas of the product lifecycle. The Patient Centered Solutions (PCS) team specializ

Associate Consultant and Statistician Statistics & Psychometrics Patient Centered SolutionsOverviewIQVIA provides scientific services spanning clinical trials real world evidence and consulting in all areas of the product lifecycle. The Patient Centered Solutions (PCS) team specializ

IQVIA is a world leader in providing actionable solutions that enable life sciences companies to innovate with confidence maximize their opportunities and ultimately drive human health outcomes forward.We at IQVIA translate healthcare data into transformative technology revolutionizin

IQVIA is a world leader in providing actionable solutions that enable life sciences companies to innovate with confidence maximize their opportunities and ultimately drive human health outcomes forward.We at IQVIA translate healthcare data into transformative technology revolutionizin

You will be involved in analyzing longitudinal patient datasets & will help our clients in making fact-based decisions. You will be working in close collaboration with different stakeholders and RWA teams across the globe. Your day-to-day activity will include working on regular stand

You will be involved in analyzing longitudinal patient datasets & will help our clients in making fact-based decisions. You will be working in close collaboration with different stakeholders and RWA teams across the globe. Your day-to-day activity will include working on regular stand

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. IQVIA offers a broad range of solutions that harness advances in healthcare information technology analytics a

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. IQVIA offers a broad range of solutions that harness advances in healthcare information technology analytics a

Research Assistant in Le CoudrayWorking Hours: Part-time 16h per weekStart Date: ImmediatelyDuration: Approximately 6 monthIQVIA is currently recruiting a dedicated Research Assistant to support a clinical research site in Le Coudray. This part-time position offers a unique opportunit

Research Assistant in Le CoudrayWorking Hours: Part-time 16h per weekStart Date: ImmediatelyDuration: Approximately 6 monthIQVIA is currently recruiting a dedicated Research Assistant to support a clinical research site in Le Coudray. This part-time position offers a unique opportunit

Country Associate Submissions Representative (Regulatory & Start-Up Specialist)HomebasedFranceIQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure collaborative culture

Country Associate Submissions Representative (Regulatory & Start-Up Specialist)HomebasedFranceIQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure collaborative culture

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 FunctionsAssist Clinical Research Associates (CRAs) and Regulatory and Star

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 FunctionsAssist Clinical Research Associates (CRAs) and Regulatory and Star

Job OverviewUnder moderate supervision executes the feasibility site identificationregulatory start-up and maintenance activities in accordance withregulations SOPs and project requirements at the regional or country level.Prepares and manages site documentation; reviews and negotiate

Job OverviewUnder moderate supervision executes the feasibility site identificationregulatory start-up and maintenance activities in accordance withregulations SOPs and project requirements at the regional or country level.Prepares and manages site documentation; reviews and negotiate