Fortrea

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

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 Clinical Research Nurse or a Paramedic to lead and support our Clinical Pharmacology Start-up team in initiating Early Phase

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 Clinical Research Nurse or a Paramedic to lead and support our Clinical Pharmacology Start-up team in initiating Early Phase

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 Clinical Research Licensed Practical Nurse (LPN) or a Paramedic to lead and support our Clinical Pharmacology Start-up team i

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 Clinical Research Licensed Practical Nurse (LPN) or a Paramedic to lead and support our Clinical Pharmacology Start-up team i

Summary of Responsibilities:For Clinical Pharmacology studies perform role of Lead Biostatistician.For Clinical Pharmacology studies maintain awareness of project budgets and tasks.Assist in the preparation of Statistical Analysis Plans (including mock TFL shells) for studies under th

Summary of Responsibilities:For Clinical Pharmacology studies perform role of Lead Biostatistician.For Clinical Pharmacology studies maintain awareness of project budgets and tasks.Assist in the preparation of Statistical Analysis Plans (including mock TFL shells) for studies under th

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

Our Phase I team is seeking an Clinical Project Manager II to join our growing team. This role requires 2 years of global project management experience with preferred experience in phase I. Candidates must be based in the United States.Job Overview:Project Managers own the operational

Our Phase I team is seeking an Clinical Project Manager II to join our growing team. This role requires 2 years of global project management experience with preferred experience in phase I. Candidates must be based in the United States.Job Overview:Project Managers own the operational

We are looking for a clinical operations professional to join our team as a Site Navigator I with a significant Start-Up experience. This is an excellent role for someone looking to grow their career in clinical research within a global CRO environment.Summary of Responsibilities:Act

We are looking for a clinical operations professional to join our team as a Site Navigator I with a significant Start-Up experience. This is an excellent role for someone looking to grow their career in clinical research within a global CRO environment.Summary of Responsibilities:Act

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

Job Overview:The Solutions Consultant Director is a senior customer-facing commercial professional responsible for supporting revenue growth by accelerating market adoption of Fortrea Intelligent Technology (FIT) solutions across FSO FSP and SaaS clinical trial delivery models. This r

Job Overview:The Solutions Consultant Director is a senior customer-facing commercial professional responsible for supporting revenue growth by accelerating market adoption of Fortrea Intelligent Technology (FIT) solutions across FSO FSP and SaaS clinical trial delivery models. This r

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

We are currently seeking Clinical Quality Operations Manager! This is a full-time role based in the United States or Canada. Job Overview:Responsible for process and performance management related to the delivery of the operational function(s) as assigned. Success in this role will re

We are currently seeking Clinical Quality Operations Manager! This is a full-time role based in the United States or Canada. Job Overview:Responsible for process and performance management related to the delivery of the operational function(s) as assigned. Success in this role will re

Job DescriptionAt Fortrea we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an internship its a launchpad for your future.As an Intern youll join a global team where curiosity motivation and fresh ideas are celebrated. Youll work on meanin

Job DescriptionAt Fortrea we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an internship its a launchpad for your future.As an Intern youll join a global team where curiosity motivation and fresh ideas are celebrated. Youll work on meanin

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:The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Sr CRA II assures the impleme

Job Overview:The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Sr CRA II assures the impleme

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