IQVIA

Account ManagerPlatform Success -IQVIA Digital (Remote)To be eligible for this position you mustresidein the same country where the job islocated.IQVIA Digital powers exceptional brand experiences delivering innovative solutions based on a customer-first insights-driven and integrated

Account ManagerPlatform Success -IQVIA Digital (Remote)To be eligible for this position you mustresidein the same country where the job islocated.IQVIA Digital powers exceptional brand experiences delivering innovative solutions based on a customer-first insights-driven and integrated

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

As the only global provider of commercial solutions IQVIA understands what it takes to deliver nationally and internationally. Our teams help biopharma medical device and diagnostic companies get their therapies to the people who need them. We help customers gain insight and access to

As the only global provider of commercial solutions IQVIA understands what it takes to deliver nationally and internationally. Our teams help biopharma medical device and diagnostic companies get their therapies to the people who need them. We help customers gain insight and access to

Personal AssistantIQIVIA Laboratories Hybrid with minimum 1 day a week in our Livingston LabThis role is ideal for an energetic and ambitious PA/EA who is early in their career and looking to take the next step in their professional development. IQVIA Laboratories is a global leader i

Personal AssistantIQIVIA Laboratories Hybrid with minimum 1 day a week in our Livingston LabThis role is ideal for an energetic and ambitious PA/EA who is early in their career and looking to take the next step in their professional development. IQVIA Laboratories is a global leader i

Job Responsibilities: Establish new processes and improve upon existing processes related to project support.Manage the set up and maintenance of all project documentation files and records according to the scope of work and SOPs.Create and coordinate all information and communication

Job Responsibilities: Establish new processes and improve upon existing processes related to project support.Manage the set up and maintenance of all project documentation files and records according to the scope of work and SOPs.Create and coordinate all information and communication

Part-time position (max. 3/4 of full time)Location: PolandJob OverviewUnder close guidance or supervision you will be responsible for creating and maintaining the IQVIA database.What to expect in this roleAssure the accuracy and timeliness of additions and modifications to the common

Part-time position (max. 3/4 of full time)Location: PolandJob OverviewUnder close guidance or supervision you will be responsible for creating and maintaining the IQVIA database.What to expect in this roleAssure the accuracy and timeliness of additions and modifications to the common

Responsibilities Ensure consistent processes and efficient review of critical clinical/safety data Review of patient-level clinical/safety data on an ongoing basis to ensure medical accuracy and completeness coding consistency and generate applicable queries as needed to obtain inform

Responsibilities Ensure consistent processes and efficient review of critical clinical/safety data Review of patient-level clinical/safety data on an ongoing basis to ensure medical accuracy and completeness coding consistency and generate applicable queries as needed to obtain inform

As the only global provider of commercial solutions IQVIA understands what it takes to deliver nationally and internationally. Our teams help biopharma medical device and diagnostic companies deliver meaningful product information to clinicians to improve patient care. We help custome

As the only global provider of commercial solutions IQVIA understands what it takes to deliver nationally and internationally. Our teams help biopharma medical device and diagnostic companies deliver meaningful product information to clinicians to improve patient care. We help custome

Role Responsibilities:Coordinate clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal InvestigatorSafeguard the well-being of subjects act as a volunteer advocate and address subject

Role Responsibilities:Coordinate clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal InvestigatorSafeguard the well-being of subjects act as a volunteer advocate and address subject

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

IQVIA is The Human Data Science Company. We use data technology analytics and human ingenuity to help healthcare clients deliver better solutions for patients and drive healthcare forward.Why this role why IQVIAJoin our Regulatory Affairs and Drug Development Solutions organization wh

IQVIA is The Human Data Science Company. We use data technology analytics and human ingenuity to help healthcare clients deliver better solutions for patients and drive healthcare forward.Why this role why IQVIAJoin our Regulatory Affairs and Drug Development Solutions organization wh

Job OverviewPlan and conduct independent audits to assess compliance with regulations guidelines and operating procedures. Prepare and distribute reports of findings to supervisor operations staff management and customers. Provide consultation in interpretation of regulations guidelin

Job OverviewPlan and conduct independent audits to assess compliance with regulations guidelines and operating procedures. Prepare and distribute reports of findings to supervisor operations staff management and customers. Provide consultation in interpretation of regulations guidelin

Phlebotomists required to cover Aberystwyth Carmarthen Pembrokeshire Llanelli and surrounding areas.Are you an experienced Phlebotomist (or a Healthcare Assistant or Nurse with phlebotomy skills) with 1 years of experience in collecting and processing venous blood samplesWe are lookin

Phlebotomists required to cover Aberystwyth Carmarthen Pembrokeshire Llanelli and surrounding areas.Are you an experienced Phlebotomist (or a Healthcare Assistant or Nurse with phlebotomy skills) with 1 years of experience in collecting and processing venous blood samplesWe are lookin

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

Associate Site Activation Manager Sponsor DedicatedDirect 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 work and resources.You will

Associate Site Activation Manager Sponsor DedicatedDirect 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 work and resources.You will

Acts as Lead Medical Writer on any type of writing project and can advise others on any type of document. Can act in a customer account management capacity and present discuss and answer questions on overall Medical Writing global capabilities to prospective customers. Performs Senior

Acts as Lead Medical Writer on any type of writing project and can advise others on any type of document. Can act in a customer account management capacity and present discuss and answer questions on overall Medical Writing global capabilities to prospective customers. Performs Senior

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

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

Role Responsibilities:Coordinate clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal InvestigatorSafeguard the well-being of subjects act as a volunteer advocate and address subject

Role Responsibilities:Coordinate clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal InvestigatorSafeguard the well-being of subjects act as a volunteer advocate and address subject

We are excited to announce we are looking for a Contact Center Quality Manager to join our team!The Contact Center Quality Manager will manage the Quality and operations functions of our Copay Contact Center programs ensuring that all program initiatives are completed in accordance wi

We are excited to announce we are looking for a Contact Center Quality Manager to join our team!The Contact Center Quality Manager will manage the Quality and operations functions of our Copay Contact Center programs ensuring that all program initiatives are completed in accordance wi

The RoleWe are looking for an experienced innovative and highly motivated engineer who is capable of working independently to design develop and support data engineering solutions. This role requires a considerable focus on understanding our data we deal with as an organization develo

The RoleWe are looking for an experienced innovative and highly motivated engineer who is capable of working independently to design develop and support data engineering solutions. This role requires a considerable focus on understanding our data we deal with as an organization develo