Home Company Detail
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
Use your scientific and foreign language expertise to join the world’s leading comprehensive pharmaceutical safety services organization at on a fast-...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
Use your scientific and foreign language expertise to join the world’s leading comprehensive pharmaceutical safety services organization at on a fast-...
The Internal Translator is responsible for linguistically and culturally interpreting the written material in a way that maintains or duplicates the s...
Job Purpose The Global CPM (Senior Study Leader) is the leader of the cross-functional clinical trial team (CTT), guides planning and management of th...
Unlock Your Potential with IQVIA Language Solutions At IQVIA Language Solutions, we stand out as the only 100% language solutions provider dedicated t...
Job overview As a Vendor Lead you will be a Single Point of Contact (SPOC) for supplier services at a trial level and be the first point for issue esc...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
Unlock Your Potential with IQVIA Language Solutions At IQVIA Language Solutions, we stand out as the only 100% language solutions provider dedicated t...
Job Purpose The Global CPM (Senior Study Leader) is the leader of the cross-functional clinical trial team (CTT), guides planning and management of th...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
Job Summary The Senior Clinical Operations Lead will be responsible to support the Clinical Trial Manager/operational team in execution of the trial(s...
IQVIA Safety Operations team play an important part in the design, build and execution of end-to-end safety solutions for major pharmaceutical compani...
Through our comprehensive training programme, you will become an expert reviewer, specializing in pharmaceutical industry compliance whilst also expan...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
Use your scientific and foreign language expertise to join the world’s leading comprehensive pharmaceutical safety services organization at on a fast-...
Job Overview Senior Global Trial Managers (SGTMs) are an integral part of clinical trial delivery, leading and working alongside clinical teams to imp...
IQVIA Safety Operations team play an important part in the design, build and execution of end-to-end safety solutions for major pharmaceutical compani...
Responsible for the end-to-end execution of the biospecimen strategy for the Global Clinical Operations supported clinical studies. Key accountabiliti...
- eSOURCE Data Acquisition Expertise. The Data Acquisition Expert performs activities relating to the definition, set-up and ingestion of External Dat...
Job Overview Senior Global Trial Managers (SGTMs) are key contributors to clinical trial delivery, leading and collaborating with clinical teams to im...
As an Associate Safety Project Manager ,* *you will be accountable for management and service delivery excellence of a range of medium to large sized...
- eSOURCE Data Acquisition Expertise. The Data Acquisition Expert performs activities relating to the definition, set-up and ingestion of External Dat...
eSOURCE Data Acquisition Expertise. The Data Acquisition Expert performs activities relating to the definition, set-up and ingestion of External Data...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
Use your scientific and foreign language expertise to join the world’s leading comprehensive pharmaceutical safety services organization at on a fast-...
IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to th...
Director, Agentic Architecture and Development Location: Europe - Home-based / Hybrid At IQVIA , we are redefining clinical development through advanc...
Director, Agentic Architecture and Development Location: Europe - Home-based / Hybrid At IQVIA , we are redefining clinical development through advanc...
Director, Agentic Architecture and Development Location: Europe - Home-based / Hybrid At IQVIA , we are redefining clinical development through advanc...
As one of our most senior engineers, you will lead the design and development of data science applications, aimed at supporting clinical trials busine...
Responsible for the end-to-end execution of the biospecimen strategy for the Global Clinical Operations supported clinical studies. Key accountabiliti...
As an Associate Safety Project Manager, you will be accountable for management and service delivery excellence of a range of medium to large-sized reg...
As an Associate Safety Project Manager, you will be responsible for managing and delivering excellent service across a range of medium to large region...
Job Overview *this role is NOT eligible for UK Visa Sponsorship Manage small to medium size Connected Devices that are stand-alone or full-service in...
Deliver high quality coordination of the centralized support by the document service management group for upload of relevant Clinical Pharmacology & P...
Through our comprehensive training programme, you will become an expert reviewer, specializing in pharmaceutical industry compliance whilst also expan...
Job Summary This position is responsible for encoding terms reported as adverse events and medical history as well as prior and concomitant medication...
The Senior Local Lab Handling Coordinator is responsible for defining and continually improving the responsibilities of the Local Lab Handling Coordin...
Global Trial Manager, Late Phase Studies, Single-Sponsor Dedicated (home-based in Europe) Join to apply for the Global Trial Manager, Late Phase Studi...
This service provides global coordination for the execution for unblinded drug management, including the general facilitation of the Independent Drug...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
Deliver high quality coordination of the centralized support by the document service management group for upload of relevant Clinical Pharmacology & P...
Lifecycle Safety Project Management team manages the delivery of lifecycle safety from trial initiation to closeout. Ensures quality deliverables are...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
Global Clinical Project Manager - Vendor Management Expert - Single Sponsor Are you an experienced Vendor Management professional looking to make an i...
Job overview Are you a Clinical (Project) IRT Manager with a passion for vendor excellence and study startup success? We're looking for a Vendor Start...
Job overview Are you a Clinical (Project) IRT Manager with a passion for vendor excellence and study startup success? We're looking for a Vendor Start...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
Job overview Are you a Clinical (Project) IRT Manager with a passion for vendor excellence and study startup success? We're looking for a Vendor Start...
Job Purpose Location: home-based, Slovakia, Poland, Bulgaria The Associate Director Senior Study Lead is the leader of the cross-functional clinical t...
Job Purpose _Location: home-based, Slovakia, Poland, Bulgaria_ The Associate Director Senior Study Lead is the leader of the cross-functional clinical...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
Therapeutic Analytics Lead Single Sponsor Are you a clinical operations professional with a passion for feasibility and strategic planning in global...
Overview Global Trial Manager, Late Phase Studies, Single-Sponsor Dedicated (home-based in Europe) – IQVIA Senior Global Trial Manager – Single Sponso...
IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to th...
Use your scientific and foreign language expertise to join the world’s leading comprehensive pharmaceutical safety services organization at on a fast-...
IQVIA is assembling a world-class team to create large-scale AI solutions, leveraging cutting-edge machine learning architectures. Our mission is to i...
Full-Stack Developer to join our application team. Requirements Seasoned developer: able to translate challenging ideas into code, create abstraction...
Full-Stack Developer to join our application team. Requirements Seasoned developer: able to translate challenging ideas into code, create abstractions...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
The person providing these services is involved in clinical out of pocket (OOP) planning from the concept phase through execution and closeout and is...
The person providing these services is involved in clinical out of pocket (OOP) planning from the concept phase through execution and closeout and is...
This unique role within IQVIA lends itself to a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication an...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
This service provides global coordination for the execution for unblinded drug management, including the general facilitation of the Independent Drug...
Full-Stack Developer to join our application team. Requirements Seasoned developer: able to translate challenging ideas into code, create abstraction...
Barcelona, Spain | Full time | Home-based | R1504643 Job available in additional locations Full-Stack Developer to join our application team. Requirem...
Full-Stack Developer to join our application team. Requirements Seasoned developer: able to translate challenging ideas into code, create abstraction...
Full-Stack Developer to join our application team. Requirements Seasoned developer: able to translate challenging ideas into code, create abstraction...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
This service provides global coordination for the execution for unblinded drug management, including the general facilitation of the Independent Drug...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
Job Overview Plan and conduct independent audits to assess compliance with regulations, guidelines, and operating procedures. Prepare and distribute r...
Job Overview Plan and conduct independent audits to assess compliance with regulations, guidelines, and operating procedures. Prepare and distribute r...
Job Overview Plan and conduct independent audits to assess compliance with regulations, guidelines, and operating procedures. Prepare and distribute r...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
Use your scientific and foreign language expertise to join the world's leading comprehensive pharmaceutical safety services organization at on a fast-...
Job Overview Plan and conduct independent audits to assess compliance with regulations, guidelines, and operating procedures. Prepare and distribute r...
Full-Stack Developer to join our application team. Requirements Seasoned developer: able to translate challenging ideas into code, create abstraction...
Full-Stack Developer to join our application team. Requirements Seasoned developer: able to translate challenging ideas into code, create abstraction...
Full-Stack Developer to join our application team. Requirements Seasoned developer: able to translate challenging ideas into code, create abstraction...
Manage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and me...
IQVIA Clinical Functional Service Partnerships (Clinical FSP) department is providing highly skilled professionals to our client's project team to set...
Full-Stack Developer to join our application team. Requirements Seasoned developer: able to translate challenging ideas into code, create abstractions...
Job Summary: We are seeking a highly skilled Data Acquisition Expert (eSource Specialist) to join our team. The ideal candidate will be responsible fo...
The Global Studies / Global Projects Lead is responsible for leading the operational delivery of one or more Phase Ib-IV clinical studies. This role o...
This is a home-based position open to candidates within the EMEA region. This service provides global coordination for the execution for unblinded dru...
This is a home-based position open to candidates within the EMEA region. This service provides global coordination for the execution for unblinded dru...
Join us on an exciting journey! If interested, PLEASE SUBMIT YOUR CV IN ENGLISH. THIS ROLE IS NOT OPEN TO VISA SPONSORSHIP THEREFORE, APPLICANTS MUST...
Join us on an exciting journey! If interested, PLEASE SUBMIT YOUR CV IN ENGLISH. THIS ROLE IS NOT OPEN TO VISA SPONSORSHIP THEREFORE, APPLICANTS MUST...
This unique role within IQVIA lends itself to a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication an...
Job overview As a Vendor Lead you will be a Single Point of Contact (SPOC) for supplier services at a trial level and be the first point for issue esc...
This unique role within IQVIA lends itself to a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication an...
This unique role within IQVIA lends itself to a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication an...
Your Mission Be the biospecimen champion in global clinical trials! Drive strategy, ensure flawless sample collection and analysis, and guarantee data...
Senior eCOA Designer Location: UK, home-based Job Overview Provides technical and domain expertise in developing, delivering and supporting eCOA busin...
Step into a role where strategy meets impact. As a Clinical Supply Chain Manager , you will shape and drive the end-to-end supply strategy for new cli...
Global Trial Manager – Single Sponsor Are you experienced in managing late phase clinical trials at a global level? We are looking for a Senior Global...
Senior Consultant and Statistician, Patient-Centered Research Overview At IQVIA, the Patient Centered Solutions team helps clients generate robust evi...
Global Trial Manager - Single Sponsor Are you experienced in managing late phase clinical trials at a global level? We are looking for a Senior Global...
Global Clinical Project Manager - Vendor Management Expert - Single Sponsor Are you an experienced Vendor Management professional looking to make an i...
External Job Description IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions f...
Job Purpose The Associate Director Senior Study Lead is the leader of the cross-functional clinical trial team (CTT), who guides planning and manageme...
We are seeking an experienced Compliance Clinical Trials Assistant to join our cFSP (sponsor-dedicated) team in EMEA. Candidates are required to have...
External Job Description IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions...
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 s...
This is a home-based position open to candidates within the EMEA region. This service provides global coordination for the execution for unblinded/unm...
Job Purpose The Associate Director Senior Study Lead is the leader of the cross-functional clinical trial team (CTT), who guides planning and manageme...
The IQVIA Clinical Functional Service Partnerships (Clinical FSP) department is providing highly skilled professionals to our client's project team to...
The person providing these services is involved in clinical out of pocket (OOP) planning from the concept phase through execution and closeout and is...
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 solu...
Global Trial Manager – Single Sponsor Are you experienced in managing late phase clinical trials at a global level? We are looking for a Senior Global...
Global Trial Manager - Single Sponsor Are you experienced in managing late phase clinical trials at a global level? We are looking for a Senior Global...
Job Overview: As a Principal Statistical Programmer you will provide advanced technical expertise to develop process methodology for the department to...
