Management, IQVIA Jobs

Role & ResponsibilitiesThe IQVIA Patient Centered Solutions group has an opportunity for a Managerto join the team to support COA Management activities. In this role you will be responsible for...

JOB OVERVIEWThe Specimen Receipt and Processing Associate is responsible for assisting with a variety of routine activities associated with receipt of clinical specimens.RESPONSIBILITIES...

Role & ResponsibilitiesThe IQVIA Patient Centered Solutions group has an opportunity for a Managerto join the team to support COA Management activities. In this role you will be responsible for...

JOB OVERVIEWThe Specimen Receipt and Processing Associate is responsible for assisting with a variety of routine activities associated with receipt of clinical specimens.RESPONSIBILITIES...

The Associate Director - Regulatory Submissions is responsible to lead a worldwide Regulatory Submissions delivery team within IQVIA Translations.This team is in charge of the development and...

External Job DescriptionJoin our Global team as a Director of Data Management!Reports to: Vice President, Data Operations or DesigneeJob Overview:Provide management and leadership for the Data...

The IQVIA Research and Development Solutions team is focused on helping our healthcare customers to find innovative treatments solutions for patients with the common, large or rarest illnesses. As...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programsRESPONSIBILITIES Acts as a Clinical...

Working with the wider Project Management team, the Team Lead is responsible for leading a team of Senior Project Managers, Project Managers and Junior Project Managers and for ensuring translation...

This is an exciting opportunity for TMF Specialist role with Informed Consent Form management experience within one of our Sponsor-dedicated Teams. Job OverviewUnder the guidance of the Global...

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...

Job OverviewProvides high quality, on-time input to client projects in the life sciences field. Assignments range in complexity from basic analysis and problem solving to assisting in the...

The Associate Director - Regulatory Submissions is responsible to lead a worldwide Regulatory Submissions delivery team within IQVIA Translations.This team is in charge of the development and...

External Job DescriptionJoin our Global team as a Director of Data Management!Reports to: Vice President, Data Operations or DesigneeJob Overview:Provide management and leadership for the Data...

The IQVIA Research and Development Solutions team is focused on helping our healthcare customers to find innovative treatments solutions for patients with the common, large or rarest illnesses. As...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programsRESPONSIBILITIES Acts as a Clinical...