Fortrea

Fortreas Clinical Research Unit in Leeds is where life-saving medicines begin their journey.Youll be part of a team that asks one crucial question: will this new medicine be safe If you enjoy working in a fast-paced environment speaking with people and contributing to meaningful resea

Fortreas Clinical Research Unit in Leeds is where life-saving medicines begin their journey.Youll be part of a team that asks one crucial question: will this new medicine be safe If you enjoy working in a fast-paced environment speaking with people and contributing to meaningful resea

Our FSP team is currently seeking a Sr. CRA 2 with 4 years of monitoring as well as strong Oncology monitoring experience residing in the Toronto Canada area. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participa

Our FSP team is currently seeking a Sr. CRA 2 with 4 years of monitoring as well as strong Oncology monitoring experience residing in the Toronto Canada area. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participa

The Solutions Consultant Digital Health and Innovation Senior Director (FIT) is a senior customer-facing commercial leader responsible for driving revenue growth by accelerating market adoption of Fortrea Intelligent Technology (FIT) solutions across FSO FSP and SaaS clinical trial de

The Solutions Consultant Digital Health and Innovation Senior Director (FIT) is a senior customer-facing commercial leader responsible for driving revenue growth by accelerating market adoption of Fortrea Intelligent Technology (FIT) solutions across FSO FSP and SaaS clinical trial de

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US. Each site does provide 24/7 rotating coverage.We are currently seeking a Screening Receptionist to support the day-to-day administration of medical scr

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US. Each site does provide 24/7 rotating coverage.We are currently seeking a Screening Receptionist to support the day-to-day administration of medical scr

The Solutions Consultant Digital Health and Innovation Senior Director (FIT) is a senior customer-facing commercial leader responsible for driving revenue growth by accelerating market adoption of Fortrea Intelligent Technology (FIT) solutions across FSO FSP and SaaS clinical trial de

The Solutions Consultant Digital Health and Innovation Senior Director (FIT) is a senior customer-facing commercial leader responsible for driving revenue growth by accelerating market adoption of Fortrea Intelligent Technology (FIT) solutions across FSO FSP and SaaS clinical trial de

Summary of Responsibilities:To respond to medical information queries/product quality complaints/general queries that may be received over the telephone call email fax etc.Receive information record and reporting Adverse Drug Reaction in timelines (according to the regulations and to

Summary of Responsibilities:To respond to medical information queries/product quality complaints/general queries that may be received over the telephone call email fax etc.Receive information record and reporting Adverse Drug Reaction in timelines (according to the regulations and to

Here in Fortrea Bulgaria we are looking for an experienced CRA to join our multisponsor team.Responsibilities:Conduct site monitoring visits (initiation routine close-out) in line with SOPs ICH-GCP and study requirementsEnsure patient safety and protocol compliance including informed

Here in Fortrea Bulgaria we are looking for an experienced CRA to join our multisponsor team.Responsibilities:Conduct site monitoring visits (initiation routine close-out) in line with SOPs ICH-GCP and study requirementsEnsure patient safety and protocol compliance including informed

Job Overview:Informatics at Fortrea is a high profile high impact team that focuses on creating innovative data-driven solutions to improve the speed cost and quality of drug development.Summary of Responsibilities:Contribute to architectural vision for Fortreas data architecture data

Job Overview:Informatics at Fortrea is a high profile high impact team that focuses on creating innovative data-driven solutions to improve the speed cost and quality of drug development.Summary of Responsibilities:Contribute to architectural vision for Fortreas data architecture data

Fortreas Full Service Team is hiring a Assoc Mgr/Manager Site Readiness! This role is remote based in the US.Job Overview:The Manager Start-up Operations is accountable for delivering on-time high quality study start-up and maintenance activities within a country or country cluster as

Fortreas Full Service Team is hiring a Assoc Mgr/Manager Site Readiness! This role is remote based in the US.Job Overview:The Manager Start-up Operations is accountable for delivering on-time high quality study start-up and maintenance activities within a country or country cluster as

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:Draft review negotiate and finalize Clinical Trial Agreements (CTAs) confidentiality agreements amendments and related site contract documentation.Coordinate with sponsors legal teams clinical operations and study teams to facilitate timely contract executi

Summary of Responsibilities:Draft review negotiate and finalize Clinical Trial Agreements (CTAs) confidentiality agreements amendments and related site contract documentation.Coordinate with sponsors legal teams clinical operations and study teams to facilitate timely contract executi

The Senior AI Trainer drives enterprise AI literacy and adoption through handson enablement and disciplined Organizational Change Management. This role designs and delivers rolebased training that enables employees to use approved AI tools safely and effectively with an initial focus

The Senior AI Trainer drives enterprise AI literacy and adoption through handson enablement and disciplined Organizational Change Management. This role designs and delivers rolebased training that enables employees to use approved AI tools safely and effectively with an initial focus

Here in Fortrea we are looking for an experienced CRA to join our miltisponsor team.Responsibilities:Conduct site monitoring visits (initiation routine close-out) in line with SOPs ICH-GCP and study requirementsEnsure patient safety and protocol compliance including informed consent a

Here in Fortrea we are looking for an experienced CRA to join our miltisponsor team.Responsibilities:Conduct site monitoring visits (initiation routine close-out) in line with SOPs ICH-GCP and study requirementsEnsure patient safety and protocol compliance including informed consent a

Join a sponsor-dedicated model supporting cutting-edge clinical trials in Germany. As a Clinical Research Associate I or Clinical Research Associate II you will contribute to high-quality clinical research delivery while gaining strong exposure to unblinded study activities in a colla

Join a sponsor-dedicated model supporting cutting-edge clinical trials in Germany. As a Clinical Research Associate I or Clinical Research Associate II you will contribute to high-quality clinical research delivery while gaining strong exposure to unblinded study activities in a colla

Prepare compile & review product quality (CMC) & other regulatory documents to support product development or submissions to various countries across the world for product registrations or post approval life cycle maintenance.Create and/or revise raw material and packaging specificati

Prepare compile & review product quality (CMC) & other regulatory documents to support product development or submissions to various countries across the world for product registrations or post approval life cycle maintenance.Create and/or revise raw material and packaging specificati

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

Join our international HR Service Delivery team in a fully homebased role anywhere in Poland supporting the DACH region with a primary focus on Germany. This role requires fluent German and English as you will handle a written HR-related queries and documentation for German-speaking e

Join our international HR Service Delivery team in a fully homebased role anywhere in Poland supporting the DACH region with a primary focus on Germany. This role requires fluent German and English as you will handle a written HR-related queries and documentation for German-speaking e

Our Phase I team is currently seeking a Clinical Research Associate with 1 years of experience. Ideal candidates would have phase I experience and reside in the Midwest preferably Dallas Texas. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a

Our Phase I team is currently seeking a Clinical Research Associate with 1 years of experience. Ideal candidates would have phase I experience and reside in the Midwest preferably Dallas Texas. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a

This role is open across Latvia Lithuania or Estonia and focuses on managing Site Navigator activities across all three Baltic countries. Candidates must have prior submissions experience within each of these countries ensuring strong local regulatory knowledge. Job Overview:Senior Si

This role is open across Latvia Lithuania or Estonia and focuses on managing Site Navigator activities across all three Baltic countries. Candidates must have prior submissions experience within each of these countries ensuring strong local regulatory knowledge. Job Overview:Senior Si

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 Clinical Research Coordinator to interact directly with our healthy volunteer participants while learning to read clinical r

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 Clinical Research Coordinator to interact directly with our healthy volunteer participants while learning to read clinical r