Fortrea

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:Informatics at Fortrea is a high profile high impact team that focuses on creating innovative data-driven solutions to improve the speed cost and quality of drug development.Summary of Responsibilities:Contribute to architectural vision for Fortreas data architecture data

Job Overview:Informatics at Fortrea is a high profile high impact team that focuses on creating innovative data-driven solutions to improve the speed cost and quality of drug development.Summary of Responsibilities:Contribute to architectural vision for Fortreas data architecture data

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

This role is for upcoming future opportunities that may arise at Fortrea.Fortrea 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

This role is for upcoming future opportunities that may arise at Fortrea.Fortrea 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

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 to interact directly with our healthy volunteer participants while learning to read clinical resear

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 to interact directly with our healthy volunteer participants while learning to read clinical resear

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

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

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: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: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

We are seeking aSponsor-Dedicated CRA IIwith solid monitoring experience. If you are eager to make an impact this is your chance!This role is to be based inBarcelonaarea.Key Responsibilities:In this role you willMonitor clinical trial sites to ensure compliance with protocols GCP and

We are seeking aSponsor-Dedicated CRA IIwith solid monitoring experience. If you are eager to make an impact this is your chance!This role is to be based inBarcelonaarea.Key Responsibilities:In this role you willMonitor clinical trial sites to ensure compliance with protocols GCP and

Our Clinical Operations department in the UK is seeking a SCRA II to work across a variety of therapeutic areas including Oncology. While you can be based anywhere in the UK previous UK monitoring experience is essential. Experience in Ophthalmology would be considered an asset.The r

Our Clinical Operations department in the UK is seeking a SCRA II to work across a variety of therapeutic areas including Oncology. While you can be based anywhere in the UK previous UK monitoring experience is essential. Experience in Ophthalmology would be considered an asset.The r

Be the connection between science and solutions.In this CRA position youll help transform complex clinical protocols into real-world results working alongside a team that values precision integrity and progress. This role will offer you the opportunity to directly influence the succes

Be the connection between science and solutions.In this CRA position youll help transform complex clinical protocols into real-world results working alongside a team that values precision integrity and progress. This role will offer you the opportunity to directly influence the succes

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:Coordinate and oversee aspects of logistics related to Clinical and Ancillary Supplies services. Support these services to both internal and external clients. Responsible for the set-up and coordination of project activities related to clinical and ancillary supplies. Ind

Job Overview:Coordinate and oversee aspects of logistics related to Clinical and Ancillary Supplies services. Support these services to both internal and external clients. Responsible for the set-up and coordination of project activities related to clinical and ancillary supplies. Ind

Job Overview:Responsible for closely partnering with IT business units to scope services that align to their strategic programs and deliverables. Helps in the leadership of financial and strategic evaluations to achieve operational effectiveness and efficiency through service introduc

Job Overview:Responsible for closely partnering with IT business units to scope services that align to their strategic programs and deliverables. Helps in the leadership of financial and strategic evaluations to achieve operational effectiveness and efficiency through service introduc

The Vice President and Head Market Access & Health Economics and Outcomes Research (HEOR) MA&HEOR role provides leadership of consulting group develops business manages client relationships and represents the business and service lines externally and internally. This individual has de

The Vice President and Head Market Access & Health Economics and Outcomes Research (HEOR) MA&HEOR role provides leadership of consulting group develops business manages client relationships and represents the business and service lines externally and internally. This individual has de

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

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 Technician 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 Clinical Research Technician to interact directly with our healthy volunteer participants while learning to read clinical res