Fortrea

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 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

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: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

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

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.

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

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 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

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:In this role youll drive revenue growth across strategic and complex accounts through proactive outreach smart networking and sharp commercial execution.Youll be the person who connects the dotscultivating key decision-maker relationships building account plans that actua

Job Overview:In this role youll drive revenue growth across strategic and complex accounts through proactive outreach smart networking and sharp commercial execution.Youll be the person who connects the dotscultivating key decision-maker relationships building account plans that actua

Fortreas Monitoring Excellence Academy is hiring!! We are seeking strong Oncology or Ophthalmology Clinical Research Coordinators or Research Nurses with 2 years of current experience. Must have 2 years of Oncology CAR T or Gen Meds as a CRC or research to various hub locations aroun

Fortreas Monitoring Excellence Academy is hiring!! We are seeking strong Oncology or Ophthalmology Clinical Research Coordinators or Research Nurses with 2 years of current experience. Must have 2 years of Oncology CAR T or Gen Meds as a CRC or research to various hub locations aroun

Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans as assigne

Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans as assigne

Job Overview:Role is primary contact for investigative sites for site payments. Responsible for administering grant and non-grant payments in accordance with the site executed agreement.Summary of Responsibilities:Accountable for the overall payment management of assigned studies whic

Job Overview:Role is primary contact for investigative sites for site payments. Responsible for administering grant and non-grant payments in accordance with the site executed agreement.Summary of Responsibilities:Accountable for the overall payment management of assigned studies whic

Job Overview:Perform and coordinate a variety of tasks to support the company as part of the leadership of the office service team.Summary of Responsibilities:Order office supplies for firm; perform associated administrative tasks including coding and assembling of invoice packages fo

Job Overview:Perform and coordinate a variety of tasks to support the company as part of the leadership of the office service team.Summary of Responsibilities:Order office supplies for firm; perform associated administrative tasks including coding and assembling of invoice packages fo

Summary of Responsibilities:Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs.Produce Define XML/PDFs Analysis Results Metadata (ARM) annotated CRFs and Reviews Guides to support SDTMs and ADaMs.All other duties as needed or assigned.Qualifications (Minimum R

Summary of Responsibilities:Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs.Produce Define XML/PDFs Analysis Results Metadata (ARM) annotated CRFs and Reviews Guides to support SDTMs and ADaMs.All other duties as needed or assigned.Qualifications (Minimum R

Location: Poland (Home-Based)At Fortrea we are advancing clinical trials through innovative risk-based approaches and data-driven oversight. We are looking for an experienced Manager Centralized & Risk-Based Monitoring & Risk-Based Quality Management (RBQM) to be part of a high-perfor

Location: Poland (Home-Based)At Fortrea we are advancing clinical trials through innovative risk-based approaches and data-driven oversight. We are looking for an experienced Manager Centralized & Risk-Based Monitoring & Risk-Based Quality Management (RBQM) to be part of a high-perfor

Fortrea is looking for Principal Biostatisticians to join our sponsor dedicated team!As a Principal Biostatistician at Fortrea you will play a crucial role in the design analysis and interpretation of clinical trials directly impacting the development of innovative therapies and treat

Fortrea is looking for Principal Biostatisticians to join our sponsor dedicated team!As a Principal Biostatistician at Fortrea you will play a crucial role in the design analysis and interpretation of clinical trials directly impacting the development of innovative therapies and treat

Summary of Responsibilities:Works with internal teams to progress quality issues in QMS.Tracks timeliness of cases in QMS.Supports teams in creation of CAPAs.Maintains strong working knowledge of QMS.Interacts with QA Lead Manager and above as required for quality issue case progressi

Summary of Responsibilities:Works with internal teams to progress quality issues in QMS.Tracks timeliness of cases in QMS.Supports teams in creation of CAPAs.Maintains strong working knowledge of QMS.Interacts with QA Lead Manager and above as required for quality issue case progressi

Job Overview:Reviews trip reports proactively identifies risks and communicate any trends outstanding issues safety concerns to the study team.Responsible for the execution of key Central monitoring activities (Site region & study level review as applicable) and collaborates with the

Job Overview:Reviews trip reports proactively identifies risks and communicate any trends outstanding issues safety concerns to the study team.Responsible for the execution of key Central monitoring activities (Site region & study level review as applicable) and collaborates with the