Fortrea

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

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

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

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

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

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 no

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 no

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

Job Overview:Performs routine laboratory sample processingSummary of Responsibilities:Follows the laboratory procedures for specimen handling and processing.Operates laboratory equipment.Recognizes deviations from expected results and follows up appropriately.Processes and ships PK sa

Job Overview:Performs routine laboratory sample processingSummary of Responsibilities:Follows the laboratory procedures for specimen handling and processing.Operates laboratory equipment.Recognizes deviations from expected results and follows up appropriately.Processes and ships PK sa

We are looking for an experienced Centralized Clinical Team Lead I / Centralized Clinical Team Lead II to oversee and drive performance within our Central Monitoring team ensuring high-quality data review and efficient study oversight.Main ResponsibilitiesLead mentor and develop a tea

We are looking for an experienced Centralized Clinical Team Lead I / Centralized Clinical Team Lead II to oversee and drive performance within our Central Monitoring team ensuring high-quality data review and efficient study oversight.Main ResponsibilitiesLead mentor and develop a tea

Summary of Responsibilities:Management of complex projects under the direction of a Project Manager/Director as assigned.Ensure site monitoring responsibility for clinical studies are conducted according to Fortrea Standard Operating Procedures (SOP) ICH Guidelines and GCP.Work closel

Summary of Responsibilities:Management of complex projects under the direction of a Project Manager/Director as assigned.Ensure site monitoring responsibility for clinical studies are conducted according to Fortrea Standard Operating Procedures (SOP) ICH Guidelines and GCP.Work closel

Senior Clinical Data Manager fully home-basedJoining Fortreas Clinical Data Management sponsor dedicated team will offer a rewarding career a chance to work in an energetic & team-oriented workplace and exposure within a world-leading team. With the support of exceptional people from

Senior Clinical Data Manager fully home-basedJoining Fortreas Clinical Data Management sponsor dedicated team will offer a rewarding career a chance to work in an energetic & team-oriented workplace and exposure within a world-leading team. With the support of exceptional people from

Were looking for a Clinical & Ancillary Supplies Services (CASS) Specialist I to support international clinical studies and drive clinical supply operations across Europe. This is a fully remote role open to candidates based in Poland Lithuania Latvia Estonia Hungary Romania or Ukrain

Were looking for a Clinical & Ancillary Supplies Services (CASS) Specialist I to support international clinical studies and drive clinical supply operations across Europe. This is a fully remote role open to candidates based in Poland Lithuania Latvia Estonia Hungary Romania or Ukrain

Join Fortrea as a Clinical Research Associate I and contribute to the delivery of highquality clinical trials that make a real difference in patients lives. This role offers an exciting opportunity to build your monitoring expertise while working in a dynamic global life sciences envi

Join Fortrea as a Clinical Research Associate I and contribute to the delivery of highquality clinical trials that make a real difference in patients lives. This role offers an exciting opportunity to build your monitoring expertise while working in a dynamic global life sciences envi

Role OverviewThe Workday Reporting & Integrations Lead is responsible for driving the design development and governance of Workday integrations and reporting solutions across Fortrea Workday HCM Workday Financials and external systems. This role ensures scalable architecture high-qual

Role OverviewThe Workday Reporting & Integrations Lead is responsible for driving the design development and governance of Workday integrations and reporting solutions across Fortrea Workday HCM Workday Financials and external systems. This role ensures scalable architecture high-qual

Role OverviewThe Workday Security Lead/Senior Manager is responsible for driving the design governance and continuous enhancement of the Workday security framework across the enterprise. This role ensures secure scalable and compliant access to sensitive data by partnering with HR Fin

Role OverviewThe Workday Security Lead/Senior Manager is responsible for driving the design governance and continuous enhancement of the Workday security framework across the enterprise. This role ensures secure scalable and compliant access to sensitive data by partnering with HR Fin

The Solutions Consultant Digital Health and Innovation Senior Director (FIT) is a senior customer-facing commercial leader responsible for driving revenue growth by accelerating market adoption of Fortrea Intelligent Technology (FIT) solutions across FSO FSP and SaaS clinical trial de

The Solutions Consultant Digital Health and Innovation Senior Director (FIT) is a senior customer-facing commercial leader responsible for driving revenue growth by accelerating market adoption of Fortrea Intelligent Technology (FIT) solutions across FSO FSP and SaaS clinical trial de

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: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: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 a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience Fortrea provides pharmaceutical biotechnology and medical device customers a wide range of clinical development patient access and technology sol

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience Fortrea provides pharmaceutical biotechnology and medical device customers a wide range of clinical development patient access and technology sol