Clinical Trials, IQVIA Jobs

PROFILEProvide insight which is exercisable across the large part of the organization or by managing a team of managers by influencing outcomes. Oversee & coordinate assigned QA program in support...

SummaryThe Design Analyst defines data needs, conducts design analytics, and develops and delivers reports and structured outputs to support protocol assessments and trial design decision making....

PROFILEProvide insight which is exercisable across the large part of the organization or by managing a team of managers by influencing outcomes. Oversee & coordinate assigned QA program in support...

SummaryThe Design Analyst defines data needs, conducts design analytics, and develops and delivers reports and structured outputs to support protocol assessments and trial design decision making....

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

Summary:The Work we do at IQVIA impacts lives all over the world. At IQVIA, the Largest Human Data Science Company in the world, we accelerate innovation for a healthier world. Come and join us to...

Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File...

PURPOSE Manages complex regulatory projects and programs and supports more junior members of the team.RESPONSIBILITIES Acts as a Clinical Trials Regulatory Manager (CTRM) on complex clinical trial...

Join us in our exciting journey!We currently require a motivated and enthusiastic clinical trials professional to join our rapidly growing international division as a Clinical Trials...

Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File...

CRA - Czech Republic - FSP - Homebased We are looking for experienced CRA to monitor clinical studies (mainly oncology) across de Czech RepublicPerform monitoring and site management work to ensure...

Are you a Registered Nurse interested in Clinical Trial work?IQVIA is looking for qualified Registered Nurses in the NYC area, interested in community and clinical trial work to visit clinical...

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

Summary:The Work we do at IQVIA impacts lives all over the world. At IQVIA, the Largest Human Data Science Company in the world, we accelerate innovation for a healthier world. Come and join us to...

Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File...

PURPOSE Manages complex regulatory projects and programs and supports more junior members of the team.RESPONSIBILITIES Acts as a Clinical Trials Regulatory Manager (CTRM) on complex clinical trial...