Fortrea

London 23 days onsite (hybrid)Are you a regulatoryfocused Study StartUp expert who thrives on ownership and compliance Were looking for a Study StartUp PM to lead countrylevel submissions approvals and site readiness for a global clientdedicated program.What youll ownOversight of en

London 23 days onsite (hybrid)Are you a regulatoryfocused Study StartUp expert who thrives on ownership and compliance Were looking for a Study StartUp PM to lead countrylevel submissions approvals and site readiness for a global clientdedicated program.What youll ownOversight of en

The Strategic Deals and Partnerships role will have global responsibility for driving strategic partnerships across biopharma accounts and other key organizations including financial entities supporting clinical trial funding. This position leads cross-functional Deal Teams to design

The Strategic Deals and Partnerships role will have global responsibility for driving strategic partnerships across biopharma accounts and other key organizations including financial entities supporting clinical trial funding. This position leads cross-functional Deal Teams to design

Job Overview:Were seeking a Solutions Architect to design and guide endtoend solutions across our Corporate Systems portfolio (Finance HR Procurement Corporate Systems). Youll partner with business and technology leaders to translate strategy and requirements into secure scalable arch

Job Overview:Were seeking a Solutions Architect to design and guide endtoend solutions across our Corporate Systems portfolio (Finance HR Procurement Corporate Systems). Youll partner with business and technology leaders to translate strategy and requirements into secure scalable arch

Job Overview:Responsible for Medical Writing activities such as appendices collation peer review and QC and publishing for designated projects and to ensure quality and compliance with Fortrea or Sponsors SOPs ICH GCP and regulatory requirements.Summary of Responsibilities:Assist with

Job Overview:Responsible for Medical Writing activities such as appendices collation peer review and QC and publishing for designated projects and to ensure quality and compliance with Fortrea or Sponsors SOPs ICH GCP and regulatory requirements.Summary of Responsibilities:Assist with

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

Job Overview:Responsible for reviewing clinical study reports patient safety narratives appendices informed consent forms clinical protocols and amendments to ensure documents are accurate consistent grammatically correct well written and logical by providing review comments and docum

Job Overview:Responsible for reviewing clinical study reports patient safety narratives appendices informed consent forms clinical protocols and amendments to ensure documents are accurate consistent grammatically correct well written and logical by providing review comments and docum

Job Overview:Assist with the overall Clinical Safety and/or departmental 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). Ensure that

Job Overview:Assist with the overall Clinical Safety and/or departmental 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). Ensure that

India Apprentice Program: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 valua

India Apprentice Program: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 valua

The Senior Director & Head of Enterprise Architecture is Fortreas most senior architecture leadership role accountable for defining and governing the enterprise technology blueprint that enables scale resilience modernization and business growth. This executive leads the Enterprise Ar

The Senior Director & Head of Enterprise Architecture is Fortreas most senior architecture leadership role accountable for defining and governing the enterprise technology blueprint that enables scale resilience modernization and business growth. This executive leads the Enterprise Ar

Job Overview:Were seeking a Solutions Architect to design and guide endtoend solutions across our Corporate Systems portfolio (Finance HR Procurement Corporate Systems). Youll partner with business and technology leaders to translate strategy and requirements into secure scalable arch

Job Overview:Were seeking a Solutions Architect to design and guide endtoend solutions across our Corporate Systems portfolio (Finance HR Procurement Corporate Systems). Youll partner with business and technology leaders to translate strategy and requirements into secure scalable arch

Job Overview:It is the responsibility of the post holder to provide all clients both internal and external with the appropriate quality of service in a safe and cost-effective manner. The individual will be expected to comply with the legal requirements of the Health and Safety at

Job Overview:It is the responsibility of the post holder to provide all clients both internal and external with the appropriate quality of service in a safe and cost-effective manner. The individual will be expected to comply with the legal requirements of the Health and Safety at

Help shape the future of riskbased clinical trial oversight.At Fortrea were transforming how clinical trials are monitoredusing data analytics and expert insight to proactively manage risk and protect patients. Were seeking a Manager or Associate Manager Central Monitoring to lead cen

Help shape the future of riskbased clinical trial oversight.At Fortrea were transforming how clinical trials are monitoredusing data analytics and expert insight to proactively manage risk and protect patients. Were seeking a Manager or Associate Manager Central Monitoring to lead cen

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

Clinical Research Associate (CRA) Drive Impact in Global Clinical TrialsAt Fortrea we are redefining whats possible in clinical research. As a global CRO built on innovation integrity and scientific excellence we empower our teams to make a meaningful impact on the future of healthca

Clinical Research Associate (CRA) Drive Impact in Global Clinical TrialsAt Fortrea we are redefining whats possible in clinical research. As a global CRO built on innovation integrity and scientific excellence we empower our teams to make a meaningful impact on the future of healthca

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

At Fortrea we help bring lifechanging treatments to patients faster. We are seeking an experienced Senior Regulatory Medical Writer to lead the development of highcomplexity clinical regulatory documents in partnership with a leading global pharmaceutical company.What You Will DoAs a

At Fortrea we help bring lifechanging treatments to patients faster. We are seeking an experienced Senior Regulatory Medical Writer to lead the development of highcomplexity clinical regulatory documents in partnership with a leading global pharmaceutical company.What You Will DoAs a

This role is for upcoming future opportunities that may arise at FortreaFortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements well invite you for an interview. If youre pre-selected our recruiter will keep in touch and let y

This role is for upcoming future opportunities that may arise at FortreaFortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements well invite you for an interview. If youre pre-selected our recruiter will keep in touch and let y

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

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