Fortrea

Job Overview:The IT Internal Communications & Marketing Intern will collaborate with the IT Clinical Platforms Executive Director to support internal communications and technology adoption initiatives for the IT and Clinical Platforms organization. The intern will help design communic

Job Overview:The IT Internal Communications & Marketing Intern will collaborate with the IT Clinical Platforms Executive Director to support internal communications and technology adoption initiatives for the IT and Clinical Platforms organization. The intern will help design communic

Job Overview:Lead the preparation and review of aggregate safety risk management signal detection and benefit-risk evaluation reports. Demonstrate the ability to independently manage the production of safety deliverables including those involving complex data analyses or important saf

Job Overview:Lead the preparation and review of aggregate safety risk management signal detection and benefit-risk evaluation reports. Demonstrate the ability to independently manage the production of safety deliverables including those involving complex data analyses or important saf

Job Overview:Provide medical safety expertise directly and indirectly to Sponsors of drugs devices and combination products in the post marketing period.Summary of Responsibilities:Undertake primary medical review of cases including medical assessment of the case for seriousness liste

Job Overview:Provide medical safety expertise directly and indirectly to Sponsors of drugs devices and combination products in the post marketing period.Summary of Responsibilities:Undertake primary medical review of cases including medical assessment of the case for seriousness liste

Job Overview:The IT Clinical Configuration Operations & Management EDC/CTMS Intern will support the Clinical Technical Configuration Team by generating operational metrics consolidating data from multiple systems and preparing monthly team performance reviews. The intern will work wit

Job Overview:The IT Clinical Configuration Operations & Management EDC/CTMS Intern will support the Clinical Technical Configuration Team by generating operational metrics consolidating data from multiple systems and preparing monthly team performance reviews. The intern will work wit

Job Overview:Provide medical safety expertise directly and indirectly to Sponsors of drugs devices and combination products in the post marketing period.Summary of Responsibilities:Undertake primary medical review of cases including medical assessment of the case for seriousness liste

Job Overview:Provide medical safety expertise directly and indirectly to Sponsors of drugs devices and combination products in the post marketing period.Summary of Responsibilities:Undertake primary medical review of cases including medical assessment of the case for seriousness liste

Job Overview:The Data Quality Analyst intern will assist with regulatory compliance risk management and the implementation of the integral management system within clinical technology systems. Responsibilities include drafting and maintaining controlled documents contacting and follow

Job Overview:The Data Quality Analyst intern will assist with regulatory compliance risk management and the implementation of the integral management system within clinical technology systems. Responsibilities include drafting and maintaining controlled documents contacting and follow

Job Overview:Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e. unsolicited reports). Manage and process ex

Job Overview:Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e. unsolicited reports). Manage and process ex

Job Overview:Lead the development and implementation of solutions to global technical services issues and concerns regarding EDC tool Medidata RAVE. Develop/validate Custom datasets (CF) and efficiently handle external data and reconciliations. Perform any postproduction changes to th

Job Overview:Lead the development and implementation of solutions to global technical services issues and concerns regarding EDC tool Medidata RAVE. Develop/validate Custom datasets (CF) and efficiently handle external data and reconciliations. Perform any postproduction changes to th

Job Overview:We are seeking an experienced Workday Configuration Analyst with deepexpertisein Record-to-Report (R2R) modules. This senior-level individual contributor role willbe responsible fordesigning building testing and deploying Workday solutions that enableaccuratefinancial rep

Job Overview:We are seeking an experienced Workday Configuration Analyst with deepexpertisein Record-to-Report (R2R) modules. This senior-level individual contributor role willbe responsible fordesigning building testing and deploying Workday solutions that enableaccuratefinancial rep

The Apprentice participates in and executes the entry level department functions (Designation of Apprentice) in accordance with Fortrea and/or sponsor Standard Operating Procedures (SOPs). Data entry of safety data onto adverse event tracking systems. Write patient narratives & code a

The Apprentice participates in and executes the entry level department functions (Designation of Apprentice) in accordance with Fortrea and/or sponsor Standard Operating Procedures (SOPs). Data entry of safety data onto adverse event tracking systems. Write patient narratives & code a

Job Overview:Lead the preparation and review of aggregate safety risk management signal detection and benefit-risk evaluation reports. Be responsible for end-to-end report management including planning authoring and managing review approval and submission steps per project scope and r

Job Overview:Lead the preparation and review of aggregate safety risk management signal detection and benefit-risk evaluation reports. Be responsible for end-to-end report management including planning authoring and managing review approval and submission steps per project scope and r

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. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in cl

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. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in cl

Exciting opportunity to be part of the Fortrea India Apprentice Program!As a Fortrea Apprentice you will have the opportunity to support meaningful assignments that compliment an education in STEM Business and Healthcare disciplines and are inspiring and valuable in our mission to imp

Exciting opportunity to be part of the Fortrea India Apprentice Program!As a Fortrea Apprentice you will have the opportunity to support meaningful assignments that compliment an education in STEM Business and Healthcare disciplines and are inspiring and valuable in our mission to imp

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 I (On-Call) to interact directly with our healthy volunteer participants while learning to read clini

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 I (On-Call) to interact directly with our healthy volunteer participants while learning to read clini

Join Fortrea as a Startup Specialist in a sponsor-dedicated role supporting clinical research for one of our key this position you will drive site activation and regulatory submissions ensuring compliance and timely delivery for global studies.This is a full-time remote role based in

Join Fortrea as a Startup Specialist in a sponsor-dedicated role supporting clinical research for one of our key this position you will drive site activation and regulatory submissions ensuring compliance and timely delivery for global studies.This is a full-time remote role based in

Job Overview:Lead writer independently responsible for the preparation of clinical study protocols and clinical study reports (CSRs) and other documents as needed for lower complexity studies. Provides support to more experienced writers with the preparation of clinical study protocol

Job Overview:Lead writer independently responsible for the preparation of clinical study protocols and clinical study reports (CSRs) and other documents as needed for lower complexity studies. Provides support to more experienced writers with the preparation of clinical study protocol

Job Overview:Providing programming and analysis support for Real World Evidence projects for Fortrea clients. Having good understanding of the various sources on Real World Data to be used in the analysis.Summary of Responsibilities:Provide programming support for analysis of real-wor

Job Overview:Providing programming and analysis support for Real World Evidence projects for Fortrea clients. Having good understanding of the various sources on Real World Data to be used in the analysis.Summary of Responsibilities:Provide programming support for analysis of real-wor

Our FSP Team is looking to hire Clinical Trial Admins in the US! Prior clinical research experience required!Job Overview:The Clinical Trial Administrator (CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree o

Our FSP Team is looking to hire Clinical Trial Admins in the US! Prior clinical research experience required!Job Overview:The Clinical Trial Administrator (CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree o

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: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