Fortrea

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

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

Job Overview:The Central Monitoring Specialist is responsible for the execution of key Central monitoring (Site subject and study level review as applicable) activities and in assisting the execution of several key activities. The Central Monitoring Specialist collaborates with the st

Job Overview:The Central Monitoring Specialist is responsible for the execution of key Central monitoring (Site subject and study level review as applicable) activities and in assisting the execution of several key activities. The Central Monitoring Specialist collaborates with the st

Job Overview:Responsible for preparation and coordination of complex clinical study protocols and clinical study reports (CSRs) and other documents as needed. Responsible for preparation of submission level documents. Provide review and feedback on documents prepared by the department

Job Overview:Responsible for preparation and coordination of complex clinical study protocols and clinical study reports (CSRs) and other documents as needed. Responsible for preparation of submission level documents. Provide review and feedback on documents prepared by the department

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: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:Manage and develop clinical operations team consisting of Clinical Research Associates. Contribute to and oversee resource planning and assignments. Provide monitoring oversight to ensure all activities are conducted to the highest possible quality and in accordance with

Job Overview:Manage and develop clinical operations team consisting of Clinical Research Associates. Contribute to and oversee resource planning and assignments. Provide monitoring oversight to ensure all activities are conducted to the highest possible quality and in accordance with

Main Responsibilities The 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

Main Responsibilities The 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

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: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