IQVIA

Regulatory & Start-Up Specialist IQVIA Biotech UKHomebasedIQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience we offer agile therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to

Regulatory & Start-Up Specialist IQVIA Biotech UKHomebasedIQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience we offer agile therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to

Our MedTech Device Field Collection Associate experiences a unique opportunity for collecting reprocessed medical equipment in a hospital. You will be working with surgical non-invasive and vascular equipment within areas of the hospital such as Operating Rooms and Sterile Processing

Our MedTech Device Field Collection Associate experiences a unique opportunity for collecting reprocessed medical equipment in a hospital. You will be working with surgical non-invasive and vascular equipment within areas of the hospital such as Operating Rooms and Sterile Processing

Job OverviewReview structured clinical patient data output without direct access to medical charts to ensure medical plausibility and determine adherence to protocol and overall completeness and readiness of the supplied patient information for next level of review.Essential Functions

Job OverviewReview structured clinical patient data output without direct access to medical charts to ensure medical plausibility and determine adherence to protocol and overall completeness and readiness of the supplied patient information for next level of review.Essential Functions

Join a team where your ideas fuel smarter solutions faster innovation and better outcomes for patients. As a Senior Business Analyst at IQVIA you will play a key role in modernizing patient support programs by translating business needs into scalable forwardthinking digital experience

Join a team where your ideas fuel smarter solutions faster innovation and better outcomes for patients. As a Senior Business Analyst at IQVIA you will play a key role in modernizing patient support programs by translating business needs into scalable forwardthinking digital experience

Principle Accountabilities: Delivering reports datasets dashboards and presentations using Sales/Rx/Patient data for US Supplier Services Responsible to write new Python / SQL / SAS codes (including using Proc SQL) and modify/enhance existing codes Responsible to develop and run scrip

Principle Accountabilities: Delivering reports datasets dashboards and presentations using Sales/Rx/Patient data for US Supplier Services Responsible to write new Python / SQL / SAS codes (including using Proc SQL) and modify/enhance existing codes Responsible to develop and run scrip

Job OverviewProvide support and guidance to less experienced members of the HR team in their day-to-day operational roles. Support the continuous improvement of the HR function through development and implementation for all HR programs in an assigned geography or assigned business lin

Job OverviewProvide support and guidance to less experienced members of the HR team in their day-to-day operational roles. Support the continuous improvement of the HR function through development and implementation for all HR programs in an assigned geography or assigned business lin

Associate Director Relational Database Services(Managed Services & Consolidation)OverviewIQVIA is seeking an Associate Director Relational Database Services to lead the transformation and operation of our global enterprise database platforms. This leader will drive a strategic shift t

Associate Director Relational Database Services(Managed Services & Consolidation)OverviewIQVIA is seeking an Associate Director Relational Database Services to lead the transformation and operation of our global enterprise database platforms. This leader will drive a strategic shift t

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 OverviewJoin our team as a Clinical Research Site Manager where youll play a crucial role in ensuring our study sites operate seamlessly and adhere to all protocols regulations and sponsor requirements.Essential FunctionsSite Monitoring:Conduct selection initiation monitoring and

Job OverviewJoin our team as a Clinical Research Site Manager where youll play a crucial role in ensuring our study sites operate seamlessly and adhere to all protocols regulations and sponsor requirements.Essential FunctionsSite Monitoring:Conduct selection initiation monitoring and

Job OverviewStudy Lead are an integral part of clinical trial delivery leading and working alongside clinical teams to improve patients lives by bringing new drugs to the market faster. The Senior Clinical Lead is a member of the core project team responsible for clinical delivery of

Job OverviewStudy Lead are an integral part of clinical trial delivery leading and working alongside clinical teams to improve patients lives by bringing new drugs to the market faster. The Senior Clinical Lead is a member of the core project team responsible for clinical delivery of

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 OverviewAssist with coordination and prioritization of department workload liaising with Project Management and Investigator Services groups (comes out). Ensure accuracy of shipments of laboratory test kits and ancillary supplies. Provide leadership to team in absence of superviso

Job OverviewAssist with coordination and prioritization of department workload liaising with Project Management and Investigator Services groups (comes out). Ensure accuracy of shipments of laboratory test kits and ancillary supplies. Provide leadership to team in absence of superviso

IQVIA Biotech is seeking a Clinical Project Manager with at least 2 years experience in project management in Immuno-oncology and Cell & Gene Therapy.IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and

IQVIA Biotech is seeking a Clinical Project Manager with at least 2 years experience in project management in Immuno-oncology and Cell & Gene Therapy.IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and

Job OverviewWith applicable guidance responsible for remote site monitoring and study delivery activities to ensure sites are conducting the study(ies) and reporting study data as required by the study protocol applicable regulations and guidelines and sponsor requirements. May monito

Job OverviewWith applicable guidance responsible for remote site monitoring and study delivery activities to ensure sites are conducting the study(ies) and reporting study data as required by the study protocol applicable regulations and guidelines and sponsor requirements. May monito

As a global leader in commercial solutions IQVIA is uniquely positioned to deliver results both nationally and internationally. Our teams partner with biopharma companies to bring essential medicines to the people who need them most. We empower our clients with insights and access to

As a global leader in commercial solutions IQVIA is uniquely positioned to deliver results both nationally and internationally. Our teams partner with biopharma companies to bring essential medicines to the people who need them most. We empower our clients with insights and access to

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience we offer agile therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.We are seeking a strategic and experienced

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience we offer agile therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.We are seeking a strategic and experienced

Under moderate supervision the Sr. Site Activation Specialist 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

Under moderate supervision the Sr. Site Activation Specialist 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

Job OverviewUnder general supervision perform tasks at a country level associated with site activation activities in accordance withapplicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines.The Cont

Job OverviewUnder general supervision perform tasks at a country level associated with site activation activities in accordance withapplicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines.The Cont

Internal Job DescriptionUnder moderate supervision the Site Activation Specialist 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 manage

Internal Job DescriptionUnder moderate supervision the Site Activation Specialist 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 manage

Job OverviewResponsible for the endtoend execution and management of incentive compensation and Commercial Operations activities within the Global Commercial Solutions (CS) organization. This role owns global Commercial Operations KPIs partners with country and global teams to drive p

Job OverviewResponsible for the endtoend execution and management of incentive compensation and Commercial Operations activities within the Global Commercial Solutions (CS) organization. This role owns global Commercial Operations KPIs partners with country and global teams to drive p