Fortrea

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 Paramedic III to interact directly with our healthy volunteer participants while learning to read clinical research protocols a

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 Paramedic III to interact directly with our healthy volunteer participants while learning to read clinical research protocols a

The Marketing Senior Manager for the Therapy Area Marketing supports the development and execution of therapyspecific marketing strategies that advance business priorities and customer engagement. This role works closely with scientific clinical and commercial stakeholders to translat

The Marketing Senior Manager for the Therapy Area Marketing supports the development and execution of therapyspecific marketing strategies that advance business priorities and customer engagement. This role works closely with scientific clinical and commercial stakeholders to translat

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

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

We are seeking a motivated Junior Developer Intern to join our pharmaceutical IT team focusing on automating business processes using modern platforms. Youll gain hands-on experience designing and deploying automation solutions that support clinical regulatory and enterprise workflows

We are seeking a motivated Junior Developer Intern to join our pharmaceutical IT team focusing on automating business processes using modern platforms. Youll gain hands-on experience designing and deploying automation solutions that support clinical regulatory and enterprise workflows

We are currently seeking Experienced Oncology CRA 2s to lead and support our Full Service Outsourcing team. CAR-T desired. Open to major hub locations on the East & West Coast. 60-70% travel 8-10 DOS per month. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgem

We are currently seeking Experienced Oncology CRA 2s to lead and support our Full Service Outsourcing team. CAR-T desired. Open to major hub locations on the East & West Coast. 60-70% travel 8-10 DOS per month. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgem

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:TheCentralized Study Specialist IIis a pivotal member of a Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to theCentralized Study Specialist IIshall reflect their experience and level of contribution which the

Job Overview:TheCentralized Study Specialist IIis a pivotal member of a Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to theCentralized Study Specialist IIshall reflect their experience and level of contribution which the

Job Overview:Perform various project management and regulatory affairs activities for Fortrea team including performance reviews human resource issues and assist Senior Management in assigning resources to projects as required. Manage coordinate and oversee the overall Regulatory Ope

Job Overview:Perform various project management and regulatory affairs activities for Fortrea team including performance reviews human resource issues and assist Senior Management in assigning resources to projects as required. Manage coordinate and oversee the overall Regulatory Ope

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

Join Our Team and Shape the Future of Clinical Research!At Fortrea we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist you will play a critical role in negotiating and managing site agreements confide

Join Our Team and Shape the Future of Clinical Research!At Fortrea we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist you will play a critical role in negotiating and managing site agreements confide

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

Summary of Responsibilities:Coordinates and oversees Regulatory Authority Ethics Committee/Institutional Review Board Third Body submissions for all study types across multiple countries globally including EU CTR through CTIS platform.Develops submission strategies timelines and progr

Summary of Responsibilities:Coordinates and oversees Regulatory Authority Ethics Committee/Institutional Review Board Third Body submissions for all study types across multiple countries globally including EU CTR through CTIS platform.Develops submission strategies timelines and progr

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: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: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

Love writing. Thrive on deadlines. Interested in clinical researchWere hiring an RFI Associate to support global business development opportunities in a fastpaced CRO environment. Youll help manage RFIs endtoend reviewing requirements pulling inputs from SMEs drafting and QCing conte

Love writing. Thrive on deadlines. Interested in clinical researchWere hiring an RFI Associate to support global business development opportunities in a fastpaced CRO environment. Youll help manage RFIs endtoend reviewing requirements pulling inputs from SMEs drafting and QCing conte

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

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

This role supports CPS. We are looking for candidates who have contract management experience in particular the generation of change orders and work orders.Summary of Responsibilities:Develop and review contracts for low to medium complexity projects and see through to execution (incl

This role supports CPS. We are looking for candidates who have contract management experience in particular the generation of change orders and work orders.Summary of Responsibilities:Develop and review contracts for low to medium complexity projects and see through to execution (incl

Fortrea is currently seeking a US remote based Clinical Data Strategy & Delivery Lead FSP to drive and support process development.This is an (exempt) full-time home-based position in the USA that will require willingness to work flexible hours as needed to meet business needs.WHAT YO

Fortrea is currently seeking a US remote based Clinical Data Strategy & Delivery Lead FSP to drive and support process development.This is an (exempt) full-time home-based position in the USA that will require willingness to work flexible hours as needed to meet business needs.WHAT YO