Management, IQVIA Jobs in England

IQVIA™ Real-World Evidence (RWE) teams work with clients to help them collect and use real-world data to generate evidence to meet the needs of regulators, payers, providers and patients. Our...

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

IQVIA™ Real-World Evidence (RWE) teams work with clients to help them collect and use real-world data to generate evidence to meet the needs of regulators, payers, providers and patients. Our...

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

Flexible location across EuropeJob OverviewYou will be responsible for overseeing complex project delivery lead by the EMEA PPG Software Development & Support Team to our EMEA Provider, Payer and...

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...

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

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...

Flexible location across EuropeJob OverviewYou will be responsible for overseeing complex project delivery lead by the EMEA PPG Software Development & Support Team to our EMEA Provider, Payer and...

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...

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

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...