Fortrea

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

This role is open to candidates based in Brazil Argentina Chile Peru Colombia Mexico Guatemala and Costa Rica.Are you passionate about turning data into insights that drive better business decisions Were looking for a Senior Metrics Analyst to join our Intelligence & Insights team and

This role is open to candidates based in Brazil Argentina Chile Peru Colombia Mexico Guatemala and Costa Rica.Are you passionate about turning data into insights that drive better business decisions Were looking for a Senior Metrics Analyst to join our Intelligence & Insights team and

Join Our Team and Drive Clinical Research Success!We are looking for German speaking candidates based in one of the following countries: Austria Switzerland UK Poland Hungary Germany Romania Denmark CzechiaAt Fortrea we are committed to accelerating clinical trials and ensuring regula

Join Our Team and Drive Clinical Research Success!We are looking for German speaking candidates based in one of the following countries: Austria Switzerland UK Poland Hungary Germany Romania Denmark CzechiaAt Fortrea we are committed to accelerating clinical trials and ensuring regula

Job Overview:Provides support to the Regional Manager of Compensation including data collection salary surveys job evaluation and report preparation. Assists in global processes such as compensation review cycles and ensures accuracy confidentiality and compliance in compensation-rela

Job Overview:Provides support to the Regional Manager of Compensation including data collection salary surveys job evaluation and report preparation. Assists in global processes such as compensation review cycles and ensures accuracy confidentiality and compliance in compensation-rela

Job Overview: The Head of Global Procurement Service Center reports directly to the Chief Procurement Officer and is responsible for matrix managing the local Bangalore resources that report to procurement leaders that are not local to Bangalore. This team consists of individuals that

Job Overview: The Head of Global Procurement Service Center reports directly to the Chief Procurement Officer and is responsible for matrix managing the local Bangalore resources that report to procurement leaders that are not local to Bangalore. This team consists of individuals that

Job Overview:The Platform Reliability & Observability Lead (SRE) will own and elevate the reliability availability and operational excellence of its hosting and platform services. This is an engineering led role accountable for measurable reliability outcomes across cloud and hybrid e

Job Overview:The Platform Reliability & Observability Lead (SRE) will own and elevate the reliability availability and operational excellence of its hosting and platform services. This is an engineering led role accountable for measurable reliability outcomes across cloud and hybrid e

The CPS organization is seeking a Senior Director or Executive Director Quality Enablement to provide enterprise-level leadership in defining governing and advancing quality oversight across early-phase and pharmacology studies. This role is critical to shaping CPS quality strategy an

The CPS organization is seeking a Senior Director or Executive Director Quality Enablement to provide enterprise-level leadership in defining governing and advancing quality oversight across early-phase and pharmacology studies. This role is critical to shaping CPS quality strategy an

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

Fortrea is looking for an experienced Clinical Trial Assistant to support global clinical studies within an FSP model for a leading pharmaceutical sponsor.What youll do:Support clinical trials endtoend in close collaboration with Clinical Project Managers and CROsManage study document

Fortrea is looking for an experienced Clinical Trial Assistant to support global clinical studies within an FSP model for a leading pharmaceutical sponsor.What youll do:Support clinical trials endtoend in close collaboration with Clinical Project Managers and CROsManage study document

Main ResponsibilitiesThe Central Monitoring Specialist is responsible for the execution of key Central Monitoring (Site subject & study level review as applicable) activities and in assisting the execution of several key activities.The Central Monitoring Specialist collaborates with t

Main ResponsibilitiesThe Central Monitoring Specialist is responsible for the execution of key Central Monitoring (Site subject & study level review as applicable) activities and in assisting the execution of several key activities.The Central Monitoring Specialist collaborates with t

Are you looking to grow your career in clinical research Fortrea is hiring CRAs at various seniority levels - CRA II and Senior CRA - to join our dynamic FSP team. We have opportunities across the UK particularly in the South East London and the Midlands offering an exciting chance to

Are you looking to grow your career in clinical research Fortrea is hiring CRAs at various seniority levels - CRA II and Senior CRA - to join our dynamic FSP team. We have opportunities across the UK particularly in the South East London and the Midlands offering an exciting chance to

Are you looking to grow your career in clinical research Fortrea is hiring a CRA II to join our dynamic FSP team. We have opportunities across the UK particularly in London offering an exciting chance to work on diverse studies while ensuring compliance with regulatory guidelines and

Are you looking to grow your career in clinical research Fortrea is hiring a CRA II to join our dynamic FSP team. We have opportunities across the UK particularly in London offering an exciting chance to work on diverse studies while ensuring compliance with regulatory guidelines and

Job Overview:The Director Workday Lead is a people leader responsible for guiding the strategic direction governance and operational excellence of the Workday platform across Finance and related enterprise functions. This role oversees a team of Workday specialists and serves as the t

Job Overview:The Director Workday Lead is a people leader responsible for guiding the strategic direction governance and operational excellence of the Workday platform across Finance and related enterprise functions. This role oversees a team of Workday specialists and serves as the t

Job Overview:Responsible for performing practical/administrative activities of clinical trials in Clinical Pharmacology in line with protocol and regulatory requirements.Summary of Responsibilities:Accurately perform blood pressure pulse weights respiratory rate and temperature readin

Job Overview:Responsible for performing practical/administrative activities of clinical trials in Clinical Pharmacology in line with protocol and regulatory requirements.Summary of Responsibilities:Accurately perform blood pressure pulse weights respiratory rate and temperature readin

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. Supervisor to interact directly with our healthy volunteer participants while learning to read clinical research protocol

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. Supervisor to interact directly with our healthy volunteer participants while learning to read clinical research protocol

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

Are you passionate about making a real impact on global healthcare We are seeking an exceptional Sr Biostatistics Manager (RWE) to join our dynamic Consulting team dedicated to advancing Real-World Evidence (RWE) this pivotal role as an individual contributor youll be at the forefron

Are you passionate about making a real impact on global healthcare We are seeking an exceptional Sr Biostatistics Manager (RWE) to join our dynamic Consulting team dedicated to advancing Real-World Evidence (RWE) this pivotal role as an individual contributor youll be at the forefron

Job Overview:Assist with the overall Safety system implementation support configuration and Migration related activities. Responsible for providing this service to clients either as a support function to the client project groups or as stand- alone business. Responsible for providing

Job Overview:Assist with the overall Safety system implementation support configuration and Migration related activities. Responsible for providing this service to clients either as a support function to the client project groups or as stand- alone business. Responsible for providing

Job Overview:Assist with the overall Clinical Safety and/or departmental 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 p

Job Overview:Assist with the overall Clinical Safety and/or departmental 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 p

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