Fortrea

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

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

At 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 meaningful projects l

At 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 meaningful projects l

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

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

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

Fortrea is looking for an experienced clinical operations professional to join our team as Senior Site Navigator (remote) with a strong focus on clinical trial start-up activities and advanced in-house CRA responsibilities. This role is ideal for someone with strong start-up expertise

Fortrea is looking for an experienced clinical operations professional to join our team as Senior Site Navigator (remote) with a strong focus on clinical trial start-up activities and advanced in-house CRA responsibilities. This role is ideal for someone with strong start-up expertise

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

Senior Clinical Data Manager FSP / oncology experienceThe Senior Clinical Data Manager role is a great opportunity to work within our sponsor dedicated department and have this unique relationship with a sponsor. You will be responsible for the full cycle of Clinical Data Management

Senior Clinical Data Manager FSP / oncology experienceThe Senior Clinical Data Manager role is a great opportunity to work within our sponsor dedicated department and have this unique relationship with a sponsor. You will be responsible for the full cycle of Clinical Data Management

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

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

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

Reports directly to the FSP CRO Line Manager.Receives study-specific requests and operational guidance from the Site Engagement Leads Head of Site Engagement and Clinical Project Manager.Serve as the face of the to develop/strengthen relationships with new/current clinical trial inves

Reports directly to the FSP CRO Line Manager.Receives study-specific requests and operational guidance from the Site Engagement Leads Head of Site Engagement and Clinical Project Manager.Serve as the face of the to develop/strengthen relationships with new/current clinical trial inves

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

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

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 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

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

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

Job Overview:Data Management leadership on studies and take responsibility for the development of the project documentation system set-up data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all DM activities (from study star

Job Overview:Data Management leadership on studies and take responsibility for the development of the project documentation system set-up data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all DM activities (from study star