Fortrea

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 FortreaJob 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 p

This role is for upcoming future opportunities that may arise at FortreaJob 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 p

Job Overview:Are you ready to shape the future of clinical research through strategic product leadershipWere looking for aProduct Managerwith deep industry expertise especially inData Management / Safety Systems /Risk based Quality / TMF / Resource Management platforms and toolsthat s

Job Overview:Are you ready to shape the future of clinical research through strategic product leadershipWere looking for aProduct Managerwith deep industry expertise especially inData Management / Safety Systems /Risk based Quality / TMF / Resource Management platforms and toolsthat s

Location: London (Hybrid) - 23 days/week on-siteWere looking for an experienced Clinical Research Manager to lead country-level clinical trial operations. Youll ensure performance quality and compliance across assigned protocols manage vendors and sites and collaborate with internal t

Location: London (Hybrid) - 23 days/week on-siteWere looking for an experienced Clinical Research Manager to lead country-level clinical trial operations. Youll ensure performance quality and compliance across assigned protocols manage vendors and sites and collaborate with internal t

Fortrea 2026 University Internship ProgramClinical Costing DepartmentLocation: UK remoteFull-time 12-monthStart Date: July 2026KICKSTART YOUR CAREER IN LIFE SCIENCESAt Fortrea we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an internshipi

Fortrea 2026 University Internship ProgramClinical Costing DepartmentLocation: UK remoteFull-time 12-monthStart Date: July 2026KICKSTART YOUR CAREER IN LIFE SCIENCESAt Fortrea we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an internshipi

We are currently seeking Experienced Sr. CRAs residing in Chicago & on the West Coast to join our FSP team!WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situ

We are currently seeking Experienced Sr. CRAs residing in Chicago & on the West Coast to join our FSP team!WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situ

12-month University Student Internship Global Proposals Leeds - Start Date July 2026At 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 a Global Proposals Intern youll join a glo

12-month University Student Internship Global Proposals Leeds - Start Date July 2026At 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 a Global Proposals Intern youll join a glo

*** Must have previous administrative as well as customer client or patient facing experience ***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 Receptionist I to interact

*** Must have previous administrative as well as customer client or patient facing experience ***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 Receptionist I to interact

Summary of Responsibilities:Supports or manages all aspects of the appropriate proposal process (text quote budget and/or response to Requests for Information RFIs) for opportunities as assigned.Responsible for managing opportunities of low to medium complexity.Shadow and/or assist mo

Summary of Responsibilities:Supports or manages all aspects of the appropriate proposal process (text quote budget and/or response to Requests for Information RFIs) for opportunities as assigned.Responsible for managing opportunities of low to medium complexity.Shadow and/or assist mo

We are seeking a skilled QA Engineer with expertise in automation testing to join our dynamic team.We are looking for a QA Engineer with a minimum of 3-5 years of experience in automation testing using Playwright and Rest Assured. The ideal candidate will also have experience with Azu

We are seeking a skilled QA Engineer with expertise in automation testing to join our dynamic team.We are looking for a QA Engineer with a minimum of 3-5 years of experience in automation testing using Playwright and Rest Assured. The ideal candidate will also have experience with Azu

Remote Work locations:East Coast USUKWestern EUJob Overview:This leader will report into the Chief Quality Regulatory and Sustainability Officer along with the leaders of the Clinical Pharmacology Services QA team the Head of the Global Quality Office and the ESG Leader. Collectively

Remote Work locations:East Coast USUKWestern EUJob Overview:This leader will report into the Chief Quality Regulatory and Sustainability Officer along with the leaders of the Clinical Pharmacology Services QA team the Head of the Global Quality Office and the ESG Leader. Collectively

We are currently seeking an experienced Medical Device CRA II residing in the Midwest or West Coast Job Overview:The CRA 2 is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and

We are currently seeking an experienced Medical Device CRA II residing in the Midwest or West Coast Job Overview:The CRA 2 is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and

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

We are seeking a skilled QA Engineer with expertise in automation testing to join our dynamic team.We are looking for a QA Engineer with a minimum of 4-6 years of experience in automation testing using Playwright and Rest Assured. The ideal candidate will also have experience with Azu

We are seeking a skilled QA Engineer with expertise in automation testing to join our dynamic team.We are looking for a QA Engineer with a minimum of 4-6 years of experience in automation testing using Playwright and Rest Assured. The ideal candidate will also have experience with Azu

Summary of Responsibilities:Perform Lead Biostatistician role on simple studies providing statistical oversight and attending relevant project meetings.Maintain awareness of project budgets and tasks and effectively communicate their status to line management and the project manager a

Summary of Responsibilities:Perform Lead Biostatistician role on simple studies providing statistical oversight and attending relevant project meetings.Maintain awareness of project budgets and tasks and effectively communicate their status to line management and the project manager a

We are currently seeking Experienced Oncology CRAs residing in the North Central (ILMNMOIAKA) or West Coast (CAAZ)!WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emerge

We are currently seeking Experienced Oncology CRAs residing in the North Central (ILMNMOIAKA) or West Coast (CAAZ)!WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emerge

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 setting (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 setting (i.e. unsolicited reports). Manage and process ex

We are currently seeking experienced Oncology CRAs residing in the Florida to join our FSP team.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 a

We are currently seeking experienced Oncology CRAs residing in the Florida to join our FSP team.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 a

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 role will offer you the opportunity todirectly influence the success of global cli

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 role will offer you the opportunity todirectly influence the success of global cli

Job Overview:The Senior Clinical Trial Administrator (Sr. CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the Sr. CTA shall reflect their experience and level of contribution whi

Job Overview:The Senior Clinical Trial Administrator (Sr. CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the Sr. CTA shall reflect their experience and level of contribution whi