Fortrea

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

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: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: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

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

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

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

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

Lead Global Growth Inspire Teams and Shape the Future at FortreaJoin Fortrea as our Global Head of FSP Sales!Are you a visionary leader ready to drive innovation and growth in the life sciences industry Fortrea is seeking an exceptional Vice President to lead our global FSP global sal

Lead Global Growth Inspire Teams and Shape the Future at FortreaJoin Fortrea as our Global Head of FSP Sales!Are you a visionary leader ready to drive innovation and growth in the life sciences industry Fortrea is seeking an exceptional Vice President to lead our global FSP global sal