Fortrea

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: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

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

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

Job Overview:Performs independent programming activities (using Medidata Rave) on multiple projects concurrently with less or no support from Senior Programmers. Development and implementation of solutions to global technical service issues and concerns regarding EDC tools like Medida

Job Overview:Performs independent programming activities (using Medidata Rave) on multiple projects concurrently with less or no support from Senior Programmers. Development and implementation of solutions to global technical service issues and concerns regarding EDC tools like Medida

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

We are currently seeking Experienced CRAs to lead and support our Full Service Outsourcing team supporting various sponsors. Oncology or Ophthalmology desired seeking candidates on the East and West Coast of Canada. French Speaking candidates also desired. Will conduct 8-10 DOS per mo

We are currently seeking Experienced CRAs to lead and support our Full Service Outsourcing team supporting various sponsors. Oncology or Ophthalmology desired seeking candidates on the East and West Coast of Canada. French Speaking candidates also desired. Will conduct 8-10 DOS per mo

Our FSP team is currently seeking a Sr. CRA 2 with 4 years of monitoring as well as strong Oncology monitoring experience residing on the West Coast (California Arizona Colorado Oregon Washington Nevada Utah Idaho New Mexico Wyoming). WHAT YOU WILL DOYou will utilize your skills knowl

Our FSP team is currently seeking a Sr. CRA 2 with 4 years of monitoring as well as strong Oncology monitoring experience residing on the West Coast (California Arizona Colorado Oregon Washington Nevada Utah Idaho New Mexico Wyoming). WHAT YOU WILL DOYou will utilize your skills knowl

Lead Teams. Elevate Operations. Drive StartUp Excellence.Were looking for an inspiring Clinical Operations Manager to lead a team of 20 professionals across clinical operations ensuring excellence in performance quality compliance and delivery.In addition to core Clinical Operations

Lead Teams. Elevate Operations. Drive StartUp Excellence.Were looking for an inspiring Clinical Operations Manager to lead a team of 20 professionals across clinical operations ensuring excellence in performance quality compliance and delivery.In addition to core Clinical Operations

Job Overview:Support site(s) by providing guidance and EHS knowledge to help minimize employee illness and injuries. Assist in ensuring compliance with regulatory requirements and relevant industry standards and help identify and lower EHS-related risks such as fires and environmental

Job Overview:Support site(s) by providing guidance and EHS knowledge to help minimize employee illness and injuries. Assist in ensuring compliance with regulatory requirements and relevant industry standards and help identify and lower EHS-related risks such as fires and environmental

Job Overview:Minimum 23-year experience in a similar job in pharmaceutical companies international CRO or providers of clinical digital servicesReports directly to the FSP Fortrea Line Manager.Receives projects-specific requests and strategic-operational guidance from the Head of Clin

Job Overview:Minimum 23-year experience in a similar job in pharmaceutical companies international CRO or providers of clinical digital servicesReports directly to the FSP Fortrea Line Manager.Receives projects-specific requests and strategic-operational guidance from the Head of Clin