Fortrea

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

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

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: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

*** 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

Summary of Responsibilities:Lead complex studies such as NDA submissions or complex multi-protocol programs potentially coordinating activities across multiple locations providing statistical oversight and attending relevant project meetings.Perform project management activities for i

Summary of Responsibilities:Lead complex studies such as NDA submissions or complex multi-protocol programs potentially coordinating activities across multiple locations providing statistical oversight and attending relevant project meetings.Perform project management activities for i

Job Overview:Assist with the 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 and process exp

Job Overview:Assist with the 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 and process exp

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 Overview:Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites this r

Job Overview:Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites this r

Job Overview:Assist with the 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 and process exp

Job Overview:Assist with the 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 and process exp

Join Fortrea as a Senior Clinical Research Associate II within a sponsor-dedicated model where you will work exclusively with a leading global biopharmaceutical this role you will support the delivery of high-quality clinical trials across innovative therapies building strong site re

Join Fortrea as a Senior Clinical Research Associate II within a sponsor-dedicated model where you will work exclusively with a leading global biopharmaceutical this role you will support the delivery of high-quality clinical trials across innovative therapies building strong site re

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

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 a Sr. GMP Quality Specialist to lead and support our Clinical Pharmacology Start-up team in initiating Early Phase clinical tri

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 a Sr. GMP Quality Specialist to lead and support our Clinical Pharmacology Start-up team in initiating Early Phase clinical tri

Job Overview:Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites this r

Job Overview:Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites this r

Job Overview:Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites th

Job Overview:Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites th

Job Overview:Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites this r

Job Overview:Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites this r

Fortrea is continuously looking for new talents! We are currently searching for Start-Up Specialist for our Sponsor-dedicated department:Responsibilities (but not only):Serve as primary contact for investigative sites and ensure documents required are collected in a timely manner.May

Fortrea is continuously looking for new talents! We are currently searching for Start-Up Specialist for our Sponsor-dedicated department:Responsibilities (but not only):Serve as primary contact for investigative sites and ensure documents required are collected in a timely manner.May