IQVIA

Clinical Trials Regulatory Officer Maintenance AssociateHome-BasedMake an impact on patient health!The Global Site Activation unit within IQVIA has the vision to be the clear market leader in clinical trial site activation driving best in class employee site and customer experiences

Clinical Trials Regulatory Officer Maintenance AssociateHome-BasedMake an impact on patient health!The Global Site Activation unit within IQVIA has the vision to be the clear market leader in clinical trial site activation driving best in class employee site and customer experiences

Job Description SummaryJob OverviewOversees supervises and manages the operational aspects of ongoing projects and programs ensuring quality deliverables on time and within budget. Will ensure that all project work is completed in accordance with SOPs policies and practices. Manage st

Job Description SummaryJob OverviewOversees supervises and manages the operational aspects of ongoing projects and programs ensuring quality deliverables on time and within budget. Will ensure that all project work is completed in accordance with SOPs policies and practices. Manage st

Role PurposeThe Customer Success Manager plays a key role in ensuring that IQVIAs healthcare clients derive maximum value from our solutions and services. The role focuses 70% on ensuring overall client satisfaction and service excellence and 30% on securing renewals and identifying o

Role PurposeThe Customer Success Manager plays a key role in ensuring that IQVIAs healthcare clients derive maximum value from our solutions and services. The role focuses 70% on ensuring overall client satisfaction and service excellence and 30% on securing renewals and identifying o

Our MedTech RN Clinical Educators experiences a unique opportunity to employ their clinical nursing expertise in a new way outside patient care while continuing to collaborate with healthcare professionals and advocate for the well-being of patients through medical device technology.

Our MedTech RN Clinical Educators experiences a unique opportunity to employ their clinical nursing expertise in a new way outside patient care while continuing to collaborate with healthcare professionals and advocate for the well-being of patients through medical device technology.

This Role is based in Jeddah.Contract Duration - 1 year.Position Overview:We are looking for a highly organized and proactive Event Logistics and Governance Coordinator to handle the planning execution and management of events logistics and governance processes.The ideal candidate wil

This Role is based in Jeddah.Contract Duration - 1 year.Position Overview:We are looking for a highly organized and proactive Event Logistics and Governance Coordinator to handle the planning execution and management of events logistics and governance processes.The ideal candidate wil

Job OverviewIncludes providing education to health care prescribers their staff patients and care givers on the proper use of designated treatments for assigned disease area o r reinforcement of study protocols as related to a clinical trial.Essential Functions Work according to the s

Job OverviewIncludes providing education to health care prescribers their staff patients and care givers on the proper use of designated treatments for assigned disease area o r reinforcement of study protocols as related to a clinical trial.Essential Functions Work according to the s

Internal Medical Translator/In-house Linguist -Spanish (ES) & French into EnglishLocation: Europe - 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

Internal Medical Translator/In-house Linguist -Spanish (ES) & French into EnglishLocation: Europe - 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

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

Join IQVIA as a Clinical Research Associate 1 or Clinical Research Associate 2 / CRA I or CRA II and work home-based throughout Germany in our single sponsor department.You will enjoy the stability and resources of a leading global contract research organization while gaining direct e

Join IQVIA as a Clinical Research Associate 1 or Clinical Research Associate 2 / CRA I or CRA II and work home-based throughout Germany in our single sponsor department.You will enjoy the stability and resources of a leading global contract research organization while gaining direct e

Ready to shape the future of healthcare through data innovation At IQVIA we harness one of the worlds largest healthcare datasets to power transformative digital products and AI-driven solutions. As a Product Manager youll play a pivotal role in building scalable data platforms that e

Ready to shape the future of healthcare through data innovation At IQVIA we harness one of the worlds largest healthcare datasets to power transformative digital products and AI-driven solutions. As a Product Manager youll play a pivotal role in building scalable data platforms that e

As Local Trial Manager you will be responsible for running international/global studies in all therapeutic areas managing the operational aspects of projects to meet contractual requirements. You will act as primary point of contact in CZ Republic to lead manage and co-ordinate the co

As Local Trial Manager you will be responsible for running international/global studies in all therapeutic areas managing the operational aspects of projects to meet contractual requirements. You will act as primary point of contact in CZ Republic to lead manage and co-ordinate the co

Imagine shaping the future of healthcare through data. At IQVIA we harness the power of advanced analytics and cutting-edge technology to improve patient outcomes worldwide. As a Senior Data Engineer youll lead the design of scalable data solutions mentor talented engineers and work o

Imagine shaping the future of healthcare through data. At IQVIA we harness the power of advanced analytics and cutting-edge technology to improve patient outcomes worldwide. As a Senior Data Engineer youll lead the design of scalable data solutions mentor talented engineers and work o

Responsibilities:Provide support to the Project Manager and related team members by performing routine procedures and tasks associated with the day to day running of projects throughout the entire study lifecycle (e.g. start-up maintenance and close-out). Ensure work is conducted in l

Responsibilities:Provide support to the Project Manager and related team members by performing routine procedures and tasks associated with the day to day running of projects throughout the entire study lifecycle (e.g. start-up maintenance and close-out). Ensure work is conducted in l

Job OverviewProject Management Analysts (PMA) are an integral part of clinical trial delivery liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The PMA works in partnership with the Project Leader (PL)/Clinical Project Manager (CPM) pro

Job OverviewProject Management Analysts (PMA) are an integral part of clinical trial delivery liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The PMA works in partnership with the Project Leader (PL)/Clinical Project Manager (CPM) pro

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.Role Location: Belgium Essential Functions Perform site

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.Role Location: Belgium Essential Functions Perform site

As the only global provider of commercial solutions IQVIA understands what it takes to deliver nationally and internationally. Our teams help biopharma get their medicines to the people who need them. We help customers gain insight and access to their markets and ultimately demonstrat

As the only global provider of commercial solutions IQVIA understands what it takes to deliver nationally and internationally. Our teams help biopharma get their medicines to the people who need them. We help customers gain insight and access to their markets and ultimately demonstrat

Job OverviewDirects financial planning and accounting practices including: budgeting costing financial analysis and long-range forecasting for a mid-sized market or regional function(s). Partners with the business providing subject matter expertise and direction for the business/funct

Job OverviewDirects financial planning and accounting practices including: budgeting costing financial analysis and long-range forecasting for a mid-sized market or regional function(s). Partners with the business providing subject matter expertise and direction for the business/funct

Job OverviewWithin a structured program supports Medical Writing deliverables and focuses on specific tasks under senior supervision while gaining experience knowledge and skills in Medical Writing. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SO

Job OverviewWithin a structured program supports Medical Writing deliverables and focuses on specific tasks under senior supervision while gaining experience knowledge and skills in Medical Writing. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SO

Medical Writing is organised as a global group of around approximately 100 Medical Writing staff in US/Brazil India Europe South Africa Ghana Japan China/Taiwan Australia New Zealand.The group mostly prepares study protocols and clinical study reports for Phase I-III interventional c

Medical Writing is organised as a global group of around approximately 100 Medical Writing staff in US/Brazil India Europe South Africa Ghana Japan China/Taiwan Australia New Zealand.The group mostly prepares study protocols and clinical study reports for Phase I-III interventional c

We are seeking an experienced Clinical Research Associate fully sponsor-dedicated with a strong background in oncology trials. This is an excellent opportunity to advance your career within a leading global CRO where youll work in a stable supportive and international environment that

We are seeking an experienced Clinical Research Associate fully sponsor-dedicated with a strong background in oncology trials. This is an excellent opportunity to advance your career within a leading global CRO where youll work in a stable supportive and international environment that