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

The RCM Billing Manager will be responsible for all processes and resources related to billing procedures including project / contract setup invoicing processing rebates and processing credits and rebills but not limited to the following:Summary of Responsibilities: Effectively manage

The RCM Billing Manager will be responsible for all processes and resources related to billing procedures including project / contract setup invoicing processing rebates and processing credits and rebills but not limited to the following:Summary of Responsibilities: Effectively manage

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: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

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

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

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

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

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

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: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

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

Key responsibilities:Design and set-up of study database for data collection in clinical trials based on protocol needsSet up of models and performing transformation updates in DMWMapping of metadata and clinical data from source system(s) to DMW (Data Management Workbench) / CDW (Cli

Key responsibilities:Design and set-up of study database for data collection in clinical trials based on protocol needsSet up of models and performing transformation updates in DMWMapping of metadata and clinical data from source system(s) to DMW (Data Management Workbench) / CDW (Cli

Job Overview:Lead the preparation and review of aggregate safety risk management signal detection and benefit-risk evaluation reports. Be responsible for end-to-end report management including planning authoring and managing review approval and submission steps per project scope and r

Job Overview:Lead the preparation and review of aggregate safety risk management signal detection and benefit-risk evaluation reports. Be responsible for end-to-end report management including planning authoring and managing review approval and submission steps per project scope and r

Summary of Responsibilities:Based on forecast models manage the resources to meet or exceed business Service Level Agreements.Supervise Mentor Evaluate and aid in staff development career development people skills and achievement of competency standards.Oversee EDC User account activa

Summary of Responsibilities:Based on forecast models manage the resources to meet or exceed business Service Level Agreements.Supervise Mentor Evaluate and aid in staff development career development people skills and achievement of competency standards.Oversee EDC User account activa

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