Fortrea

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:The Chief Accounting Officer is a senior Finance leader responsible for Fortreas global accounting external reporting internal controls and compliance environment. This role leads the accounting organization including record-to-report and payroll-related accounting proces

Job Overview:The Chief Accounting Officer is a senior Finance leader responsible for Fortreas global accounting external reporting internal controls and compliance environment. This role leads the accounting organization including record-to-report and payroll-related accounting proces

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

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 I / Part-Time to interact directly with our healthy volunteer participants while learning to read clinical res

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 I / Part-Time to interact directly with our healthy volunteer participants while learning to read clinical res

Job Overview:Lead the development and implementation of solutions to global technical services issues and concerns regarding EDC tools like Medidata RAVE or Oracle Inform or Data/Report programming or Visual Analytics tools like Spotfire or Tableau. Develop/validate Custom/Complex SAS

Job Overview:Lead the development and implementation of solutions to global technical services issues and concerns regarding EDC tools like Medidata RAVE or Oracle Inform or Data/Report programming or Visual Analytics tools like Spotfire or Tableau. Develop/validate Custom/Complex SAS

Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study to ensure EC/IRB/Third body/Regulatory Authority and any other local applications

Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study to ensure EC/IRB/Third body/Regulatory Authority and any other local applications

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:Clinical Development Strategy & Business Partner serves as a strategic and operational partner to a Clinical Delivery leader. This role translates business strategy into execution plans monitors performance metrics and drives process improvements within the assigned depar

Job Overview:Clinical Development Strategy & Business Partner serves as a strategic and operational partner to a Clinical Delivery leader. This role translates business strategy into execution plans monitors performance metrics and drives process improvements within the assigned depar

Job Overview:The Senior CRA 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 assure the implementation of project plans as assigned. F

Job Overview:The Senior CRA 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 assure the implementation of project plans as assigned. F

The Proposal Manager is responsible for leading and coordinating the end-to-end proposal development process for low to medium complexity opportunities ensuring the delivery of high-quality compliant and competitive proposals that align with client requirements and Fortreas strategic

The Proposal Manager is responsible for leading and coordinating the end-to-end proposal development process for low to medium complexity opportunities ensuring the delivery of high-quality compliant and competitive proposals that align with client requirements and Fortreas strategic

Your Role at Fortrea:As a Medical Contact Center Assistant I you will be the voice of support for healthcare professionals and patients addressing medical information queries product quality complaints and general inquiries. You will also be responsible for receiving recording and rep

Your Role at Fortrea:As a Medical Contact Center Assistant I you will be the voice of support for healthcare professionals and patients addressing medical information queries product quality complaints and general inquiries. You will also be responsible for receiving recording and rep

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all asp

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all asp

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all asp

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all asp

Are you passionate about developing people driving operational excellence and shaping the future of clinical researchWe are looking for a Manager II Clinical Operations to lead a team of clinical research professionals across the UK/IRE. This is an exciting opportunity to play a key l

Are you passionate about developing people driving operational excellence and shaping the future of clinical researchWe are looking for a Manager II Clinical Operations to lead a team of clinical research professionals across the UK/IRE. This is an exciting opportunity to play a key l

About the TeamThe Inside Sales EU team plays a critical role in identifying new opportunities building connections and creating pipelines for business growth. As part of this team youll support Inside Sales Managers by assisting with prospecting researching potential leads across Euro

About the TeamThe Inside Sales EU team plays a critical role in identifying new opportunities building connections and creating pipelines for business growth. As part of this team youll support Inside Sales Managers by assisting with prospecting researching potential leads across Euro

Fortrea is one of the worlds largest and longest-established early-phase clinical research organizations. From first-in-human to exploratory biomarker or complex ph1b programs our Clinical Pharmacology team generate critical safety tolerability PK and PD data that help new medicines t

Fortrea is one of the worlds largest and longest-established early-phase clinical research organizations. From first-in-human to exploratory biomarker or complex ph1b programs our Clinical Pharmacology team generate critical safety tolerability PK and PD data that help new medicines t

Fortreas Clinical Research Unit in Leeds is where life-saving medicines begin their journey.Job Overview:Responsible for handling all public inquiries pertaining to study participation. Schedules screening appointments for suitable participants.This is a Bank (0-hours) position where

Fortreas Clinical Research Unit in Leeds is where life-saving medicines begin their journey.Job Overview:Responsible for handling all public inquiries pertaining to study participation. Schedules screening appointments for suitable participants.This is a Bank (0-hours) position where

Fortrea is recruiting!Our FSO department in Paris is looking fora Senior Clinical Research Associate I (SCRA I).Key Responsibilities:Monitor Clinical Trials -conduct site visits to ensure compliance with protocols regulatory requirements and Good Clinical Practice (GCP) - National on

Fortrea is recruiting!Our FSO department in Paris is looking fora Senior Clinical Research Associate I (SCRA I).Key Responsibilities:Monitor Clinical Trials -conduct site visits to ensure compliance with protocols regulatory requirements and Good Clinical Practice (GCP) - National on

Join Our Team and Drive Clinical Research Success!AtFortrea we are committed to accelerating clinical trials and ensuring regulatory compliance. As aSite Start-Up Specialist Iyou will play a pivotal role in coordinating site start-up activities managing essential documents and ensurin

Join Our Team and Drive Clinical Research Success!AtFortrea we are committed to accelerating clinical trials and ensuring regulatory compliance. As aSite Start-Up Specialist Iyou will play a pivotal role in coordinating site start-up activities managing essential documents and ensurin

Summary of Responsibilities:Owns all aspects of the appropriate proposal process (text quote budget and/or response to Requests for Information RFIs) for assigned opportunities (inclusive of managing opportunities under general supervision establishing clear timelines meeting client r

Summary of Responsibilities:Owns all aspects of the appropriate proposal process (text quote budget and/or response to Requests for Information RFIs) for assigned opportunities (inclusive of managing opportunities under general supervision establishing clear timelines meeting client r