IQVIA

Analyst (Management Consulting)Sydney / Melbourne OnlyIQVIA has an exciting opportunity for an Analyst to be part of the Management Consulting Business Unit within our Sydney or Melbourne office.This role will see you apply every aspect of your experience and qualifications together w

Analyst (Management Consulting)Sydney / Melbourne OnlyIQVIA has an exciting opportunity for an Analyst to be part of the Management Consulting Business Unit within our Sydney or Melbourne office.This role will see you apply every aspect of your experience and qualifications together w

Job OverviewPrimarily acts as back-up Medical Advisor but may serve as Regional Medical Advisor on assigned projects. Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications inclusion/exclusion determinations and

Job OverviewPrimarily acts as back-up Medical Advisor but may serve as Regional Medical Advisor on assigned projects. Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications inclusion/exclusion determinations and

LocationOffice-based in Irving TXJob SummaryThe Regulatory Affairs Coordinator will act as liaison between NEXT Oncology the Institutional Review Board and various Pharmaceutical and Biotech companies (Sponsors) to open clinical trials at NEXT Oncology.Essential Duties and Responsibil

LocationOffice-based in Irving TXJob SummaryThe Regulatory Affairs Coordinator will act as liaison between NEXT Oncology the Institutional Review Board and various Pharmaceutical and Biotech companies (Sponsors) to open clinical trials at NEXT Oncology.Essential Duties and Responsibil

Global Trial Manager Single Sponsor Are you experienced in managing late phase clinical trials at a global levelWe are looking for a Senior Global Trial Manager to join our Single Sponsor Department. Join our global team and take ownership of delivering late-phase clinical trials tha

Global Trial Manager Single Sponsor Are you experienced in managing late phase clinical trials at a global levelWe are looking for a Senior Global Trial Manager to join our Single Sponsor Department. Join our global team and take ownership of delivering late-phase clinical trials tha

The Part Time Clinical Consultant (PTCC) role is an exciting opportunity to join IQVIA. IQVIA/MedTech takes the approach to helping customers drive healthcare forward in this challenging fast-paced environment. We help customers accelerate results improve patient outcomes and unleash

The Part Time Clinical Consultant (PTCC) role is an exciting opportunity to join IQVIA. IQVIA/MedTech takes the approach to helping customers drive healthcare forward in this challenging fast-paced environment. We help customers accelerate results improve patient outcomes and unleash

The Part Time Clinical Consultant (PTCC) role is an exciting opportunity to join IQVIA. IQVIA/MedTech takes the approach to helping customers drive healthcare forward in this challenging fast-paced environment. We help customers accelerate results improve patient outcomes and unleash

The Part Time Clinical Consultant (PTCC) role is an exciting opportunity to join IQVIA. IQVIA/MedTech takes the approach to helping customers drive healthcare forward in this challenging fast-paced environment. We help customers accelerate results improve patient outcomes and unleash

Job Title: Patient Support Program (PSP) ManagerLocation: Gauteng South Africa (supporting projects across English-speaking African markets)Role OverviewWe are seeking an experienced Patient Support Program (PSP) Manager to take ownership of the end-to-end operational quality and comp

Job Title: Patient Support Program (PSP) ManagerLocation: Gauteng South Africa (supporting projects across English-speaking African markets)Role OverviewWe are seeking an experienced Patient Support Program (PSP) Manager to take ownership of the end-to-end operational quality and comp

Study Start Up Clinical Research AssociateIQVIA is looking for talented and motivated team member to join our Sponsor dedicated team as Study Start Up Clinical Research Associate. At this position you would be responsible of site preparation and early identification of real site needs

Study Start Up Clinical Research AssociateIQVIA is looking for talented and motivated team member to join our Sponsor dedicated team as Study Start Up Clinical Research Associate. At this position you would be responsible of site preparation and early identification of real site needs

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

Project Role: Software Development Engineer 3Work Experience: 4 to 7 YearsWork location: ChennaiWork Mode: Hybrid (Working from the Chennai office during the first week of every month)Must Have Skills: AngularJS Job Overview:Under guidance performs activities related to the analysi

Project Role: Software Development Engineer 3Work Experience: 4 to 7 YearsWork location: ChennaiWork Mode: Hybrid (Working from the Chennai office during the first week of every month)Must Have Skills: AngularJS Job Overview:Under guidance performs activities related to the analysi

We are seeking Specimen Receipt & Processing Associate (42633) to join IQVIA Laboratories at Valencia.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 transfor

We are seeking Specimen Receipt & Processing Associate (42633) to join IQVIA Laboratories at Valencia.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 transfor

Study Start-Up - Clinical Research Associate (SSU CRA)Sponsor dedicated less travellingCRA 1- Sr CRA 1 levelOverview:The Study Start-Up CRA is accountable for site selections as well as study-specific start-up activities and deliverables in the country. Proactive site preparation and

Study Start-Up - Clinical Research Associate (SSU CRA)Sponsor dedicated less travellingCRA 1- Sr CRA 1 levelOverview:The Study Start-Up CRA is accountable for site selections as well as study-specific start-up activities and deliverables in the country. Proactive site preparation and

Job Profile SummaryThe Associate Director Commercial Operations Reporting Lead is a senior role within the Global Commercial Solutions organisation responsible for designing governing and continuously improving the end-to-end commercial reporting ecosystem across all RBUs and GBUs. T

Job Profile SummaryThe Associate Director Commercial Operations Reporting Lead is a senior role within the Global Commercial Solutions organisation responsible for designing governing and continuously improving the end-to-end commercial reporting ecosystem across all RBUs and GBUs. T

The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our clients project team in the execution of clinical trials. Joining the team provides the opportunity to manage Early Phase clinical research projects in different therapeuti

The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our clients project team in the execution of clinical trials. Joining the team provides the opportunity to manage Early Phase clinical research projects in different therapeuti

Job OverviewPrimarily acts as back-up Medical Advisor but may serve as Regional Medical Advisor on assigned projects. Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications inclusion/exclusion determinations and

Job OverviewPrimarily acts as back-up Medical Advisor but may serve as Regional Medical Advisor on assigned projects. Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications inclusion/exclusion determinations and

Clinical Research Associate Your responsibilities will include:Performing site selection initiation monitoring and close-out visits after completing training periodSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accorda

Clinical Research Associate Your responsibilities will include:Performing site selection initiation monitoring and close-out visits after completing training periodSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accorda

About the RoleWe are looking for a Market Access / Product Specialist to bridge the gap between business regulation and product development. This is a unique hybrid role combining product thinking with strong analytical and domain expertise in market access pricing or healthcare-relat

About the RoleWe are looking for a Market Access / Product Specialist to bridge the gap between business regulation and product development. This is a unique hybrid role combining product thinking with strong analytical and domain expertise in market access pricing or healthcare-relat

Lead Developer / Engineering Team Lead (Backend Focus)About the RoleWe are looking for a hands-on Lead Developer to guide a small high-performing engineering team while driving the evolution of our product platform. This role combines technical leadership architecture ownership and te

Lead Developer / Engineering Team Lead (Backend Focus)About the RoleWe are looking for a hands-on Lead Developer to guide a small high-performing engineering team while driving the evolution of our product platform. This role combines technical leadership architecture ownership and te

Join a great team of young & smart talents!The purpose of the General Ledger (GL) accountant is to ensure correct accounting information and reporting mainly in the area of inventory and intercompany. You will gather and verify the accuracy of financial data and reconcile accounts. Th

Join a great team of young & smart talents!The purpose of the General Ledger (GL) accountant is to ensure correct accounting information and reporting mainly in the area of inventory and intercompany. You will gather and verify the accuracy of financial data and reconcile accounts. Th

Job OverviewDevelop and prepare budgets and proposals for assigned customers to support the global sales team.;Essential Functions Review Requests For Proposal (RFP). Identify information for proposal text and budget development and work closely with proposal development team to prepa

Job OverviewDevelop and prepare budgets and proposals for assigned customers to support the global sales team.;Essential Functions Review Requests For Proposal (RFP). Identify information for proposal text and budget development and work closely with proposal development team to prepa