Fortrea

Job Overview:Collaborate with peers across the organization to achieve client-centric delivery in a matrix organization. Collaboration across all stakeholders within Site Readiness. Oversight and accountability of Regulatory Authority (RA) Independent Review Board (IRB)/Ethics Committ

Job Overview:Collaborate with peers across the organization to achieve client-centric delivery in a matrix organization. Collaboration across all stakeholders within Site Readiness. Oversight and accountability of Regulatory Authority (RA) Independent Review Board (IRB)/Ethics Committ

Job Overview:In the role you will collaborate with key stakeholders across the organization and at times be client facing to achieve client-centric delivery in a matrix organization. Oversight and accountability of Regulatory Authority (RA) Independent Review Board (IRB)/Ethics Commit

Job Overview:In the role you will collaborate with key stakeholders across the organization and at times be client facing to achieve client-centric delivery in a matrix organization. Oversight and accountability of Regulatory Authority (RA) Independent Review Board (IRB)/Ethics Commit

Job Overview:The Medical Writer supports client engagements and internal requests projects and business development efforts by doing the necessary research data collection analysis and interpretation; development of value messages dossiers reports and other written deliverables modeli

Job Overview:The Medical Writer supports client engagements and internal requests projects and business development efforts by doing the necessary research data collection analysis and interpretation; development of value messages dossiers reports and other written deliverables modeli

Job Overview:It is the responsibility of the post holder to provide all clients both internal and external with the appropriate quality of service in a safe and cost-effective manner. The individual will be expected to comply with the legal requirements of the Health and Safety at Wor

Job Overview:It is the responsibility of the post holder to provide all clients both internal and external with the appropriate quality of service in a safe and cost-effective manner. The individual will be expected to comply with the legal requirements of the Health and Safety at Wor

Job Overview:Assist in the development and implementation of solutions to DM service issues and concerns regarding Medidata RAVE Oracle Inform CRF Design and Data Capture or imaging activities including proactive prevention strategies. Develop and maintain programs for creation of dat

Job Overview:Assist in the development and implementation of solutions to DM service issues and concerns regarding Medidata RAVE Oracle Inform CRF Design and Data Capture or imaging activities including proactive prevention strategies. Develop and maintain programs for creation of dat

Be the connection between science and solutions.In this CRA position youll help transform complex clinical protocols into real-world results working alongside a team that values precision integrity and progress. This role will offer you the opportunity to directly influence the succes

Be the connection between science and solutions.In this CRA position youll help transform complex clinical protocols into real-world results working alongside a team that values precision integrity and progress. This role will offer you the opportunity to directly influence the succes

Job Overview:The Clinical and Ancillary Supplies Services (CASS) Specialist II: Independently support the delivery of the Clinical and Ancillary supplies component of assigned studies within a region or for a simple global study. Act as contact with study team during clinical and anci

Job Overview:The Clinical and Ancillary Supplies Services (CASS) Specialist II: Independently support the delivery of the Clinical and Ancillary supplies component of assigned studies within a region or for a simple global study. Act as contact with study team during clinical and anci

Job Overview:Senior 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

Job Overview:Senior 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

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 settings (i.e. unsolicited reports). Manage and process ex

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 settings (i.e. unsolicited reports). Manage and process ex

We are looking to hire a Clinical Team Lead (Local Trial Manager) in France. In this position you will be fully dedicated to a single sponsor. This position is open for full-time candidates.Responsibilities/Provide end-to-end operational oversight for the assigned study(ies) including

We are looking to hire a Clinical Team Lead (Local Trial Manager) in France. In this position you will be fully dedicated to a single sponsor. This position is open for full-time candidates.Responsibilities/Provide end-to-end operational oversight for the assigned study(ies) including

Our FSO team is seeking an Cell & Gene Therapy Sr. Clinical Project Manager or Project Manager II to join our growing team. This role requires 3-5 years of global project management experience with mandatory experience in cell & gene. Candidates must be based in the United States. Jo

Our FSO team is seeking an Cell & Gene Therapy Sr. Clinical Project Manager or Project Manager II to join our growing team. This role requires 3-5 years of global project management experience with mandatory experience in cell & gene. Candidates must be based in the United States. Jo

Our FSO team is seeking an Ophthalmology Senior Clinical Project Manager or Clinical Project Manager II to join our growing team. This role requires 3 years of global project management experience with mandatory experience in ophthalmology. Candidates must be based in the United State

Our FSO team is seeking an Ophthalmology Senior Clinical Project Manager or Clinical Project Manager II to join our growing team. This role requires 3 years of global project management experience with mandatory experience in ophthalmology. Candidates must be based in the United State

Job Overview:The Scientist supports client engagements by contributing to the collection and analysis of primary and secondary data andassistingin the development of client deliverables. This role focuses on executing project-specific tasks applying analytical methods and supporting p

Job Overview:The Scientist supports client engagements by contributing to the collection and analysis of primary and secondary data andassistingin the development of client deliverables. This role focuses on executing project-specific tasks applying analytical methods and supporting p

Job Overview:The Inside Sales Associate role within Fortrea Consulting is responsible for generating business opportunity leads that achieve quarterly and annual goals managing inbound client interactions and supporting business development efforts across Fortreas Consulting organizat

Job Overview:The Inside Sales Associate role within Fortrea Consulting is responsible for generating business opportunity leads that achieve quarterly and annual goals managing inbound client interactions and supporting business development efforts across Fortreas Consulting organizat

Job Overview:Manages ARC review and are responsible for performing TMF review of electronic Trial Master Files (eTMF) Trial Country and Site artifacts for clinical studies in support of sponsors services contracts and internal business needs.Summary of Responsibilities:Position provid

Job Overview:Manages ARC review and are responsible for performing TMF review of electronic Trial Master Files (eTMF) Trial Country and Site artifacts for clinical studies in support of sponsors services contracts and internal business needs.Summary of Responsibilities:Position provid

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

Senior External Data Specialist Clinical Data Management / Vendor DataThe Senior External Data Specialist role is a great opportunity to support Clinical Data Management activities focused on external vendor and laboratory data. You will contribute to ensuring high-quality consistent

Senior External Data Specialist Clinical Data Management / Vendor DataThe Senior External Data Specialist role is a great opportunity to support Clinical Data Management activities focused on external vendor and laboratory data. You will contribute to ensuring high-quality consistent

Sponsor-dedicated. Full time. Remote in the UK Spain South Africa Greece Portugal or Hungary.We are on a mission to deliver solutions that bring life-changing treatments to patients faster.But we cant do it alone. We are seeking an experienced Senior Regulatory Medical Writer to lead

Sponsor-dedicated. Full time. Remote in the UK Spain South Africa Greece Portugal or Hungary.We are on a mission to deliver solutions that bring life-changing treatments to patients faster.But we cant do it alone. We are seeking an experienced Senior Regulatory Medical Writer to lead

Summary of Responsibilities:Perform Lead Biostatistician role on medium complexity studies providing statistical oversight and attending relevant project meetings.Perform project management activities for identified projects including resource planning timelines and milestone manageme

Summary of Responsibilities:Perform Lead Biostatistician role on medium complexity studies providing statistical oversight and attending relevant project meetings.Perform project management activities for identified projects including resource planning timelines and milestone manageme

At Fortrea our world-class Clinical Research Unit in Leeds is where life-changing medicines begin their journey. Located just minutes from the train station our 65000 ft² 100-bed facility is a cornerstone of early clinical development connecting science with real-world impact.Were lo

At Fortrea our world-class Clinical Research Unit in Leeds is where life-changing medicines begin their journey. Located just minutes from the train station our 65000 ft² 100-bed facility is a cornerstone of early clinical development connecting science with real-world impact.Were lo