Fortrea

Are you passionate about clinical trial budgeting financial strategy and delivering accurate competitive study cost estimatesJoin Fortrea as an Investigator Grants Manager / Clinical Trial Costing Managerand play a critical role in shaping successful clinical research proposals and st

Are you passionate about clinical trial budgeting financial strategy and delivering accurate competitive study cost estimatesJoin Fortrea as an Investigator Grants Manager / Clinical Trial Costing Managerand play a critical role in shaping successful clinical research proposals and st

Are you passionate about clinical trial budgeting financial strategy and delivering accurate competitive study cost estimatesJoin Fortrea as an Investigator Grants Manager / Clinical Trial Costing Managerand play a critical role in shaping successful clinical research proposals and st

Are you passionate about clinical trial budgeting financial strategy and delivering accurate competitive study cost estimatesJoin Fortrea as an Investigator Grants Manager / Clinical Trial Costing Managerand play a critical role in shaping successful clinical research proposals and st

Job Overview:Manage Client or Project specific PSS 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) for specified projects. Manage and

Job Overview:Manage Client or Project specific PSS 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) for specified projects. Manage and

Our FSP team is currently seeking Sr. CRA 2s with 4 years of monitoring residing in the East Coast Midwest & West Coast US!WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clinical trials and respond t

Our FSP team is currently seeking Sr. CRA 2s with 4 years of monitoring residing in the East Coast Midwest & West Coast US!WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clinical trials and respond t

Job Overview:The Senior Director Commercial and Marketing Technology Platforms plays a pivotal role in shaping and delivering Fortreas commercial and marketing technology ecosystem. This leader is responsible for the strategy management and continuous evolution of platforms that enabl

Job Overview:The Senior Director Commercial and Marketing Technology Platforms plays a pivotal role in shaping and delivering Fortreas commercial and marketing technology ecosystem. This leader is responsible for the strategy management and continuous evolution of platforms that enabl

Risk Based Quality Management (RBQM) DirectorLocations: US Canada LATAM EMEA or IndiaApplication process closes: Friday July 17th Important: To be considered for this role all applicants must upload an up-to-date resume. A cover letter alone will not meet the application requirements.

Risk Based Quality Management (RBQM) DirectorLocations: US Canada LATAM EMEA or IndiaApplication process closes: Friday July 17th Important: To be considered for this role all applicants must upload an up-to-date resume. A cover letter alone will not meet the application requirements.

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 CRF Specialist to be responsible for transcribing and managing study data ensuring accuracy and collaborating with various st

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 CRF Specialist to be responsible for transcribing and managing study data ensuring accuracy and collaborating with various st

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

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

Job Overview:The Global Corporate Compliance & Privacy Counsel supports the design implementation and continuous improvement of Fortreas global compliance and privacy programmes. Working within a collaborative team-based counsel model the role helps maintain a consistent regulator-rea

Job Overview:The Global Corporate Compliance & Privacy Counsel supports the design implementation and continuous improvement of Fortreas global compliance and privacy programmes. Working within a collaborative team-based counsel model the role helps maintain a consistent regulator-rea

Financial Clinical Trial Assistant (CTA) Hybrid WarsawWe are looking for a dynamic and detail-oriented Financial CTA to join our client-dedicated (FSP) team in Warsaw.This role offers the opportunity to work in a fast-paced environment where youll be involved in multiple systems an

Financial Clinical Trial Assistant (CTA) Hybrid WarsawWe are looking for a dynamic and detail-oriented Financial CTA to join our client-dedicated (FSP) team in Warsaw.This role offers the opportunity to work in a fast-paced environment where youll be involved in multiple systems an

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:The Clinical Research Associate I MEA (CRA I MEA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the CRA I MEA shall reflect their experience and level of contribution w

Job Overview:The Clinical Research Associate I MEA (CRA I MEA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the CRA I MEA shall reflect their experience and level of contribution w

Job Overview:The Senior Director Strategic Accounts will serve as a strategic business partner responsible for leading complex sales efforts and developing expanding and deepening new business opportunities within assigned strategic customer accounts. This individual will play a lead

Job Overview:The Senior Director Strategic Accounts will serve as a strategic business partner responsible for leading complex sales efforts and developing expanding and deepening new business opportunities within assigned strategic customer accounts. This individual will play a lead

Job Overview:Serve as a member of the project team with primary responsibility for clinical data review query generation / resolution and reconciliation to support the delivery of clinical data according to client quality and integrity specifications and project timelines and producti

Job Overview:Serve as a member of the project team with primary responsibility for clinical data review query generation / resolution and reconciliation to support the delivery of clinical data according to client quality and integrity specifications and project timelines and producti

Roles and Responsibilities:Support the day-to-day operations of assigned activities within SSU to ensure completionperestablished goals andobjectivesin compliance with applicable GCP/ICH guidelines and other regulatory requirements. This includes effective communication and coordinati

Roles and Responsibilities:Support the day-to-day operations of assigned activities within SSU to ensure completionperestablished goals andobjectivesin compliance with applicable GCP/ICH guidelines and other regulatory requirements. This includes effective communication and coordinati

Job Overview:The CRM is accountable for execution and oversight of local operational clinical trial activities and has ownership oversight and impact on local regulatory and financial compliance at a country operations level at the client in compliance with ICH GCP and country regulat

Job Overview:The CRM is accountable for execution and oversight of local operational clinical trial activities and has ownership oversight and impact on local regulatory and financial compliance at a country operations level at the client in compliance with ICH GCP and country regulat

We are currently seeking a RWE Programmer to join a sponsor-dedicated team supporting a global pharmaceutical partner. This is a fully home-based opportunity.As a RWE Programmer you will serve as a subject matter expert in Real World Data analytics and support the analysis of large he

We are currently seeking a RWE Programmer to join a sponsor-dedicated team supporting a global pharmaceutical partner. This is a fully home-based opportunity.As a RWE Programmer you will serve as a subject matter expert in Real World Data analytics and support the analysis of large he

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

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 an Outpatient Visit (OPV) Research Nurse or a Paramedic to lead and support our Clinical Pharmacology Start-up team in initiati

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 an Outpatient Visit (OPV) Research Nurse or a Paramedic to lead and support our Clinical Pharmacology Start-up team in initiati