IQVIA

As a Consultant at IQVIA you will be responsible for the development & delivery of consulting projects. You will also be part of the regional consulting group and will have the opportunity to support larger & more complex projects in the Southeast Asia region.Participates in the desig

As a Consultant at IQVIA you will be responsible for the development & delivery of consulting projects. You will also be part of the regional consulting group and will have the opportunity to support larger & more complex projects in the Southeast Asia region.Participates in the desig

Responsibilities: Ensures the contract fulfillment to specifications of basic and routine reports for defined customers. Reviews client data requirements with the appropriate internal resource to ensure that basic product deliverables meet the customers specifications including timel

Responsibilities: Ensures the contract fulfillment to specifications of basic and routine reports for defined customers. Reviews client data requirements with the appropriate internal resource to ensure that basic product deliverables meet the customers specifications including timel

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 tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include maintenanc

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include maintenanc

Job OverviewValidates the project scope plans and schedules for moderately complex projects; adheres to metrics for project success and begins to suggest appropriate metrics; provides input to and applies standards (e.g. delivery process roles and responsibilities operational norms co

Job OverviewValidates the project scope plans and schedules for moderately complex projects; adheres to metrics for project success and begins to suggest appropriate metrics; provides input to and applies standards (e.g. delivery process roles and responsibilities operational norms co

Job OverviewManages a single department or work unit responsible for site activation. Sets goals and objectives for team members for achievement of short-term operational or tactical results. Essential Functions Manages staffs delivery of site activation activities in accordance wit

Job OverviewManages a single department or work unit responsible for site activation. Sets goals and objectives for team members for achievement of short-term operational or tactical results. Essential Functions Manages staffs delivery of site activation activities in accordance wit

Job OverviewThe Associate Stat Programming Director plays a critical role in ensuring the accuracy and integrity of statistical programming across various clinical projects. This position demands proficiency in SAS programming and familiarity with CDISC standards particularly ADaM and

Job OverviewThe Associate Stat Programming Director plays a critical role in ensuring the accuracy and integrity of statistical programming across various clinical projects. This position demands proficiency in SAS programming and familiarity with CDISC standards particularly ADaM and

Clinical Trial Psych Rater - Swedish 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. We

Clinical Trial Psych Rater - Swedish 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. We

HelpDesk Trainer and Quality SpecialistLisbon PortugalHomebased/Remote from PortugalRole Purpose:Responsible for both Help Desk Operational quality: Training and Quality Assurance.As a trainer he/she will be delivering technology application and customer service skills development ini

HelpDesk Trainer and Quality SpecialistLisbon PortugalHomebased/Remote from PortugalRole Purpose:Responsible for both Help Desk Operational quality: Training and Quality Assurance.As a trainer he/she will be delivering technology application and customer service skills development ini

Regulatory & Start Up ManagerPortugal/SpainIQVIA MedtechHomebasedJob 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 wo

Regulatory & Start Up ManagerPortugal/SpainIQVIA MedtechHomebasedJob 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 wo

Job Description SummaryJob OverviewManage end-to-end delivery of data management services for single/multi-service projects with minimal guidance ensuring quality deliverables on time and within budget to customer satisfaction. Provide comprehensive data management expertise to Clinic

Job Description SummaryJob OverviewManage end-to-end delivery of data management services for single/multi-service projects with minimal guidance ensuring quality deliverables on time and within budget to customer satisfaction. Provide comprehensive data management expertise to Clinic

Essential Functions Define and prioritize resource requirements and manage resource assignments across projects. Monitor and manage utilization and productivity of Functional Department. Assess and document competency of staff to satisfy position responsibilities. Regularly set goals

Essential Functions Define and prioritize resource requirements and manage resource assignments across projects. Monitor and manage utilization and productivity of Functional Department. Assess and document competency of staff to satisfy position responsibilities. Regularly set goals

Essential Functions With moderate oversight and supervision werve a Single Point of Contact (SPOC) to perform feasibility site activation and some maintenance activities in assigned studies for investigative sites according to applicable regulations SOPs and work instructions working

Essential Functions With moderate oversight and supervision werve a Single Point of Contact (SPOC) to perform feasibility site activation and some maintenance activities in assigned studies for investigative sites according to applicable regulations SOPs and work instructions working

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. Formed through the merger of IMS Health and Quintiles IQVIA offers a broad range of solutions that harness adv

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. Formed through the merger of IMS Health and Quintiles IQVIA offers a broad range of solutions that harness adv

The Study Physician is a critical global role responsible for assuming medical oversight of clinical trials within Clinical Development & Operations. This position requires a qualified and clinically experienced physician who will provide comprehensive medical expertise throughout all

The Study Physician is a critical global role responsible for assuming medical oversight of clinical trials within Clinical Development & Operations. This position requires a qualified and clinically experienced physician who will provide comprehensive medical expertise throughout all

We are seeking a resilient strategic and self-driven Key Account Manager (Business Access Manager m/f/d) to lead biosimilar product innovations in a client dedicated role.You will be responsible for driving market access and maximizing sales growth across your territory (Baden-Württem

We are seeking a resilient strategic and self-driven Key Account Manager (Business Access Manager m/f/d) to lead biosimilar product innovations in a client dedicated role.You will be responsible for driving market access and maximizing sales growth across your territory (Baden-Württem

Job OverviewPerform tasks in support of the Clinical Trial Submission Coordinator (CTSC) Regulatory CTA SM and GCO country teams to make all clinical trial initial submissions clinical trial amendment submissions and clinical trial notifications in CTIS and track the progress of submi

Job OverviewPerform tasks in support of the Clinical Trial Submission Coordinator (CTSC) Regulatory CTA SM and GCO country teams to make all clinical trial initial submissions clinical trial amendment submissions and clinical trial notifications in CTIS and track the progress of submi

Sr. Site Contracts AssociateIQVIA BiotechBulgaria Serbia Slovakia Czech Republic Slovakia Romania - HomebasedIQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure colla

Sr. Site Contracts AssociateIQVIA BiotechBulgaria Serbia Slovakia Czech Republic Slovakia Romania - HomebasedIQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure colla

Clinical Trial Educators (CTEs) collaborate with research staff and other stakeholders to drive trial recruitment and support study-specific training needs. The CTE acts as a strategic partner to both external and internal stakeholders to optimize the site experience and performance.

Clinical Trial Educators (CTEs) collaborate with research staff and other stakeholders to drive trial recruitment and support study-specific training needs. The CTE acts as a strategic partner to both external and internal stakeholders to optimize the site experience and performance.

IQVIA Biotech is seeking a Project Management Analyst to join our growing team in Argentina. This role will be home-based in Argentina.Job OverviewProject Management Analysts (PMA) are an integral part of clinical trial delivery liaising with clinical teams to improve patients lives b

IQVIA Biotech is seeking a Project Management Analyst to join our growing team in Argentina. This role will be home-based in Argentina.Job OverviewProject Management Analysts (PMA) are an integral part of clinical trial delivery liaising with clinical teams to improve patients lives b