Fortrea

Job Overview:Prepares and negotiates and assists in the execution and retention of site agreements confidentiality agreements letters of indemnification and other contracts for Sponsors who contract Fortrea to perform this service. Maintains and contributes to contracts tracking and s

Job Overview:Prepares and negotiates and assists in the execution and retention of site agreements confidentiality agreements letters of indemnification and other contracts for Sponsors who contract Fortrea to perform this service. Maintains and contributes to contracts tracking and s

Are you detail-oriented and passionate about supporting clinical research operations Join our team in Munich as an Administrative Project Coordinator where youll play a key role in enabling regulatory or financial workflows across clinical studies. This is a sponsor-dedicated office-b

Are you detail-oriented and passionate about supporting clinical research operations Join our team in Munich as an Administrative Project Coordinator where youll play a key role in enabling regulatory or financial workflows across clinical studies. This is a sponsor-dedicated office-b

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

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 Technician to lead and support our Clinical Pharmacology Start-up team in initiating Early Phase clinical trials for

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 Technician to lead and support our Clinical Pharmacology Start-up team in initiating Early Phase clinical trials for

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:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans as assigne

Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans as assigne

Science/chemistry graduates who have worked in regulatory affairsTranslate/create/revise raw material chemical and packaging specifications using client global specification systems as requiredTranslate/create and manage global change controls for these revisions to the raw material a

Science/chemistry graduates who have worked in regulatory affairsTranslate/create/revise raw material chemical and packaging specifications using client global specification systems as requiredTranslate/create and manage global change controls for these revisions to the raw material a

Science/chemistry graduates who have worked in regulatory affairs (more than 2 years of experience)Translate/create/revise raw material chemical and packaging specifications using client global specification systems as requiredTranslate/create and manage global change controls for the

Science/chemistry graduates who have worked in regulatory affairs (more than 2 years of experience)Translate/create/revise raw material chemical and packaging specifications using client global specification systems as requiredTranslate/create and manage global change controls for the

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

12-month University Student Placement Clinical Data Management Leeds July 2026At Fortrea we believe early talent is the heartbeat of innovation. Our Early Careers program is more than a year in industry placement: its a launchpad for your future.As a Clinical Data Management Intern

12-month University Student Placement Clinical Data Management Leeds July 2026At Fortrea we believe early talent is the heartbeat of innovation. Our Early Careers program is more than a year in industry placement: its a launchpad for your future.As a Clinical Data Management Intern

Are you a dynamic leader passionate about driving clinical trials to success We are looking for an experienced Clinical Trial Manager responsible for study oversight and delivery management (time budget quality)from start-up to closure in this role youll collaborate with sponsors inv

Are you a dynamic leader passionate about driving clinical trials to success We are looking for an experienced Clinical Trial Manager responsible for study oversight and delivery management (time budget quality)from start-up to closure in this role youll collaborate with sponsors inv

At 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 Intern youll join a global team where curiosity motivation and fresh ideas are celebrated. Youll work on meaningful projects lea

At 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 Intern youll join a global team where curiosity motivation and fresh ideas are celebrated. Youll work on meaningful projects lea

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

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:Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post marketing settings (i.e. unsolicited reports). Manage and process ex

Job Overview:Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post marketing settings (i.e. unsolicited reports). Manage and process ex

Job Overview:Leading projects and project teams for 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. Training and Mentoring the less experien

Job Overview:Leading projects and project teams for 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. Training and Mentoring the less experien

Are you looking to grow your career in clinical researchFortrea is hiring a CRAII to join our client-dedicated team. This role is based in the North West offering an exciting opportunity to work on diverse studies while ensuring compliance with regulatory guidelines and company SOPs.W

Are you looking to grow your career in clinical researchFortrea is hiring a CRAII to join our client-dedicated team. This role is based in the North West offering an exciting opportunity to work on diverse studies while ensuring compliance with regulatory guidelines and company SOPs.W

Looking for a dynamic remote role with a global CRO Become our new Medical Contact Center Assistant!If you have educational background in healthcare speak fluent English and French and are wiling to work 3pm -12pm (CET) then this is the perfect role for you!Summary of Responsibilities

Looking for a dynamic remote role with a global CRO Become our new Medical Contact Center Assistant!If you have educational background in healthcare speak fluent English and French and are wiling to work 3pm -12pm (CET) then this is the perfect role for you!Summary of Responsibilities

Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans as assigne

Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans as assigne

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 le

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 le