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

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

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 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

This role is for upcoming future opportunities that may arise at Fortrea. It is a full-time position supporting a single sponsor.Role is based in the Oslo area.Key requirement:Minimum 2 years of clinical monitoring experiencePreferably 1 year experience in oncology studiesSummary of R

This role is for upcoming future opportunities that may arise at Fortrea. It is a full-time position supporting a single sponsor.Role is based in the Oslo area.Key requirement:Minimum 2 years of clinical monitoring experiencePreferably 1 year experience in oncology studiesSummary of R

The Manager Business Intelligence leads and develops a team of Commercial analysts responsible for delivering high-quality reporting dashboards and data-driven insights that support business decision-making. This role combines people leadership hands-on analytics project management an

The Manager Business Intelligence leads and develops a team of Commercial analysts responsible for delivering high-quality reporting dashboards and data-driven insights that support business decision-making. This role combines people leadership hands-on analytics project management an

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

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