As a Senior or Principal Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit you will be central to the successful delivery of complex global oncology clinical trials (Phases IIII) for some of the worlds most renowned and innovative pharmaceutical companie

As a Senior or Principal Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit you will be central to the successful delivery of complex global oncology clinical trials (Phases IIII) for some of the worlds most renowned and innovative pharmaceutical companie

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Full Time

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 Research Nurse (RNs LPNs) 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 Research Nurse (RNs LPNs) to interact directly with our healthy volunteer participants while learning to read clinical resear

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Full Time

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 you know when the role officially opens so we can reconfirm your interest

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 you know when the role officially opens so we can reconfirm your interest

Apply Now
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

Launch Your Career with FortreaAt Fortrea we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an internshipits a launchpad for your future.As an Internyoull join a global team where curiosity motivation and fresh ideas are celebrated. Youll w

Launch Your Career with FortreaAt Fortrea we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an internshipits a launchpad for your future.As an Internyoull join a global team where curiosity motivation and fresh ideas are celebrated. Youll w

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Join Our Team and Shape the Future of Clinical Research!At Fortrea we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget Specialist you will play a critical role in the clinical trials budgeting process. Your work will help

Join Our Team and Shape the Future of Clinical Research!At Fortrea we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget Specialist you will play a critical role in the clinical trials budgeting process. Your work will help

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Are you ready to take your expertise in clinical contracts and budgeting to the next level AtFortrea we are looking for a detail-oriented and strategic professional to join our FSP team as aSite Contract Lead. In this role you will be at the forefront of clinical trial execution ensur

Are you ready to take your expertise in clinical contracts and budgeting to the next level AtFortrea we are looking for a detail-oriented and strategic professional to join our FSP team as aSite Contract Lead. In this role you will be at the forefront of clinical trial execution ensur

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Are you ready to make a meaningful impact in clinical research Join our team as a Clinical Research Associate II (CRA II) in France where youll play a key role in advancing observational and registry studies. Be part of a new dynamic model with a global Project Management hub supporti

Are you ready to make a meaningful impact in clinical research Join our team as a Clinical Research Associate II (CRA II) in France where youll play a key role in advancing observational and registry studies. Be part of a new dynamic model with a global Project Management hub supporti

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We are currently seeking Experienced Sr. CRAs fluent in Spanish residing in the Mid West US! Also open to hub airports with direct flights to Puerto Rico. This FSP aligned role works with IVD clinical trials. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgemen

We are currently seeking Experienced Sr. CRAs fluent in Spanish residing in the Mid West US! Also open to hub airports with direct flights to Puerto Rico. This FSP aligned role works with IVD clinical trials. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgemen

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Full Time

Job Overview:Assist in the development and implementation of solutions to global technical service issues and concerns regarding EDC or SAS or other proprietary software including proactive prevention strategies. Develop/validate Custom/Complex SDTM/SAS datasets/Listings/reports. Effi

Job Overview:Assist in the development and implementation of solutions to global technical service issues and concerns regarding EDC or SAS or other proprietary software including proactive prevention strategies. Develop/validate Custom/Complex SDTM/SAS datasets/Listings/reports. Effi

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Summary of Responsibilities:Follow applicable departmental Standard Operating Procedures and Work Instructions.Complete required trainings according to required timelines.Administer controlled documents ensuring availability to the end user.Track and report metrics as determined by ma

Summary of Responsibilities:Follow applicable departmental Standard Operating Procedures and Work Instructions.Complete required trainings according to required timelines.Administer controlled documents ensuring availability to the end user.Track and report metrics as determined by ma

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We are currently seeking Experienced Sr. CRAs fluent in Spanish residing in the Mid West US! Also open to hub airports with direct flights to Puerto Rico. This FSP aligned role works with IVD clinical trials. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgemen

We are currently seeking Experienced Sr. CRAs fluent in Spanish residing in the Mid West US! Also open to hub airports with direct flights to Puerto Rico. This FSP aligned role works with IVD clinical trials. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgemen

Apply Now
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

Apply Now
Full Time

Job Overview:Assist in the development and implementation of solutions to global technical service issues and concerns regarding EDC or SAS or other proprietary software including proactive prevention strategies. Develop/validate Custom/Complex SDTM/SAS datasets/Listings/reports. Effi

Job Overview:Assist in the development and implementation of solutions to global technical service issues and concerns regarding EDC or SAS or other proprietary software including proactive prevention strategies. Develop/validate Custom/Complex SDTM/SAS datasets/Listings/reports. Effi

Apply Now

We are currently seeking Experienced Oncology CRAs residing on the East Coast to join our FSP team! Various openings including Regional North East & South East roles as well as more Nationwide Travel roles seeking candidates on the East Coast & Central US. WHAT YOU WILL DOYou will uti

We are currently seeking Experienced Oncology CRAs residing on the East Coast to join our FSP team! Various openings including Regional North East & South East roles as well as more Nationwide Travel roles seeking candidates on the East Coast & Central US. WHAT YOU WILL DOYou will uti

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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:Senior manager data integration connects their technical passion and skills for integration solutions with communication and organizational management. They have a great understanding of integration concepts technology and processes for data movement across and between or

Job Overview:Senior manager data integration connects their technical passion and skills for integration solutions with communication and organizational management. They have a great understanding of integration concepts technology and processes for data movement across and between or

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Full Time

Job Overview:Perform various project management and regulatory affairs activities for Fortrea clients. Manage team including performance reviews human resource issues and assist Senior Management in assigning resources to projects as required. Manage coordinate and oversee the overall

Job Overview:Perform various project management and regulatory affairs activities for Fortrea clients. Manage team including performance reviews human resource issues and assist Senior Management in assigning resources to projects as required. Manage coordinate and oversee the overall

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Full Time

The mission of our Project Coordinator Academy is to identify early talent and develop you to become Fortrea s leaders of the future. The PC Academy prepares entry-level Project Coordinators to take on critical client-facing tasks as co-pilots to PMs enabling them to build client trus

The mission of our Project Coordinator Academy is to identify early talent and develop you to become Fortrea s leaders of the future. The PC Academy prepares entry-level Project Coordinators to take on critical client-facing tasks as co-pilots to PMs enabling them to build client trus

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At Fortrea we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an internship its a launchpad for your future.As an Intern youll join a global team where curiosity motivation and fresh ideas are celebrated. Youll work on meaningful projects l

At Fortrea we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an internship its a launchpad for your future.As an Intern youll join a global team where curiosity motivation and fresh ideas are celebrated. Youll work on meaningful projects l

Apply Now