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

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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

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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

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Full Time

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

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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

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Cra

Fortrea

Full Time

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

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Job Overview:The Clinical and Ancillary Supplies Services (CASS) Specialist I: Support the delivery of the Clinical and Ancillary supplies component of assigned studies within a country or 1 region. Act as contact with study team during clinical and ancillary start-up activities inclu

Job Overview:The Clinical and Ancillary Supplies Services (CASS) Specialist I: Support the delivery of the Clinical and Ancillary supplies component of assigned studies within a country or 1 region. Act as contact with study team during clinical and ancillary start-up activities inclu

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Full Time

We are currently seeking Sr CRAs with 4 years of monitoring within in United States. Travel is expected to be regional and about 50% overnight. Job Overview:The Senior CRA 2 is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortre

We are currently seeking Sr CRAs with 4 years of monitoring within in United States. Travel is expected to be regional and about 50% overnight. Job Overview:The Senior CRA 2 is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortre

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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

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Full Time

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

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Full Time

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

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Full Time

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

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Full Time

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

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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

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Fortrea

Full Time

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

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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

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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

Apply Now
Full Time

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

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Full Time

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

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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

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