Fortrea

The Senior AI Trainer drives enterprise AI literacy and adoption through handson enablement and disciplined Organizational Change Management. This role designs and delivers rolebased training that enables employees to use approved AI tools safely and effectively with an initial focus

The Senior AI Trainer drives enterprise AI literacy and adoption through handson enablement and disciplined Organizational Change Management. This role designs and delivers rolebased training that enables employees to use approved AI tools safely and effectively with an initial focus

Here in Fortrea we are looking for an experienced CRA to join our miltisponsor team.Responsibilities:Conduct site monitoring visits (initiation routine close-out) in line with SOPs ICH-GCP and study requirementsEnsure patient safety and protocol compliance including informed consent a

Here in Fortrea we are looking for an experienced CRA to join our miltisponsor team.Responsibilities:Conduct site monitoring visits (initiation routine close-out) in line with SOPs ICH-GCP and study requirementsEnsure patient safety and protocol compliance including informed consent a

Prepare compile & review product quality (CMC) & other regulatory documents to support product development or submissions to various countries across the world for product registrations or post approval life cycle maintenance.Create and/or revise raw material and packaging specificati

Prepare compile & review product quality (CMC) & other regulatory documents to support product development or submissions to various countries across the world for product registrations or post approval life cycle maintenance.Create and/or revise raw material and packaging specificati

Job Overview:Data Management leadership on studies and take responsibility for the development of the project documentation system set-up data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all DM activities (from study star

Job Overview:Data Management leadership on studies and take responsibility for the development of the project documentation system set-up data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all DM activities (from study star

Join our international HR Service Delivery team in a fully homebased role anywhere in Poland supporting the DACH region with a primary focus on Germany. This role requires fluent German and English as you will handle a written HR-related queries and documentation for German-speaking e

Join our international HR Service Delivery team in a fully homebased role anywhere in Poland supporting the DACH region with a primary focus on Germany. This role requires fluent German and English as you will handle a written HR-related queries and documentation for German-speaking e

Summary of Responsibilities:Draft review negotiate and finalize Clinical Trial Agreements (CTAs) confidentiality agreements amendments and related site contract documentation.Coordinate with sponsors legal teams clinical operations and study teams to facilitate timely contract executi

Summary of Responsibilities:Draft review negotiate and finalize Clinical Trial Agreements (CTAs) confidentiality agreements amendments and related site contract documentation.Coordinate with sponsors legal teams clinical operations and study teams to facilitate timely contract executi

Fortreas Full Service Team is hiring a Assoc Mgr/Manager Site Readiness! This role is remote based in the US.Job Overview:The Manager Start-up Operations is accountable for delivering on-time high quality study start-up and maintenance activities within a country or country cluster as

Fortreas Full Service Team is hiring a Assoc Mgr/Manager Site Readiness! This role is remote based in the US.Job Overview:The Manager Start-up Operations is accountable for delivering on-time high quality study start-up and maintenance activities within a country or country cluster as

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibi

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibi

Join a sponsor-dedicated model supporting cutting-edge clinical trials in Germany. As a Clinical Research Associate I or Clinical Research Associate II you will contribute to high-quality clinical research delivery while gaining strong exposure to unblinded study activities in a colla

Join a sponsor-dedicated model supporting cutting-edge clinical trials in Germany. As a Clinical Research Associate I or Clinical Research Associate II you will contribute to high-quality clinical research delivery while gaining strong exposure to unblinded study activities in a colla

This role is open across Latvia Lithuania or Estonia and focuses on managing Site Navigator activities across all three Baltic countries. Candidates must have prior submissions experience within each of these countries ensuring strong local regulatory knowledge. Job Overview:Senior Si

This role is open across Latvia Lithuania or Estonia and focuses on managing Site Navigator activities across all three Baltic countries. Candidates must have prior submissions experience within each of these countries ensuring strong local regulatory knowledge. Job Overview:Senior Si

Our Phase I team is currently seeking a Clinical Research Associate with 1 years of experience. Ideal candidates would have phase I experience and reside in the Midwest preferably Dallas Texas. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a

Our Phase I team is currently seeking a Clinical Research Associate with 1 years of experience. Ideal candidates would have phase I experience and reside in the Midwest preferably Dallas Texas. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a

Job Overview:Responsible for assisting with overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e. unsolicited reports). Manage

Job Overview:Responsible for assisting with overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e. unsolicited reports). Manage

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking an Clinical Research Coordinator to interact directly with our healthy volunteer participants while learning to read clinical r

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking an Clinical Research Coordinator to interact directly with our healthy volunteer participants while learning to read clinical r

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibi

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibi

Summary of Responsibilities:Contributes to generation of global QA policies on interpretation or application.Provides subject matter GxP expertise and influences the ED/CS/CDS organization by providing guidance and client/authority facing support on specific regulatory topics and Qual

Summary of Responsibilities:Contributes to generation of global QA policies on interpretation or application.Provides subject matter GxP expertise and influences the ED/CS/CDS organization by providing guidance and client/authority facing support on specific regulatory topics and Qual

Job Overview:The Principal Consultant Senior Director within Fortrea Consulting is an experienced consultant and researcher focused on strategizing and building client relationships across a broad spectrum of consulting areas (e.g. clinical development realworld evidence (RWE) health

Job Overview:The Principal Consultant Senior Director within Fortrea Consulting is an experienced consultant and researcher focused on strategizing and building client relationships across a broad spectrum of consulting areas (e.g. clinical development realworld evidence (RWE) health

*** Experience working in a management/leadership role within a CRO (Clinical Research Organization) and understanding of GCP (Good Clinical Practices) is strongly preferred ***As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Researc

*** Experience working in a management/leadership role within a CRO (Clinical Research Organization) and understanding of GCP (Good Clinical Practices) is strongly preferred ***As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Researc

***Experience in the following areas required: Phlebotomy taking vital signs and extreme attention to detail.***As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US. Each site does provide 24/7 rotating co

***Experience in the following areas required: Phlebotomy taking vital signs and extreme attention to detail.***As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US. Each site does provide 24/7 rotating co

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all asp

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all asp

Job DescriptionOur FSP team is currently seeking an Oncology Sr. CRA 2 with 5 years of monitoring residing in the Midwest (ILINIAKSMIMNMONDSDWI OH) area.WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in

Job DescriptionOur FSP team is currently seeking an Oncology Sr. CRA 2 with 5 years of monitoring residing in the Midwest (ILINIAKSMIMNMONDSDWI OH) area.WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in