Fortrea

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.Were looking for a Clinical Pharmacist to play a key role in supporting clinical trials and ensuring the safe and compliant handling of investigational

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.Were looking for a Clinical Pharmacist to play a key role in supporting clinical trials and ensuring the safe and compliant handling of investigational

Shape the Future of Data at FortreaAre you a visionary leader in data architecture and integration Fortrea is seeking a Chief Data Officer to drive the strategy and execution of services that will deliver the future state for Fortreas global data platforms.The role will require the de

Shape the Future of Data at FortreaAre you a visionary leader in data architecture and integration Fortrea is seeking a Chief Data Officer to drive the strategy and execution of services that will deliver the future state for Fortreas global data platforms.The role will require the de

The Director of Product Engineering will lead the strategy and development of our Data Management Products. This role is pivotal in shaping innovative solutions that meet the evolving needs of our clients in the life science sector. The successful candidate will bridge the gap between

The Director of Product Engineering will lead the strategy and development of our Data Management Products. This role is pivotal in shaping innovative solutions that meet the evolving needs of our clients in the life science sector. The successful candidate will bridge the gap between

Fortrea is recruiting an experienced Clinical Project Manager with valuable expertise in this role you will ensure the successful execution of clinical studies on a local level while maintaining high-quality standards and regulatory compliance. Please note this role is for upcoming f

Fortrea is recruiting an experienced Clinical Project Manager with valuable expertise in this role you will ensure the successful execution of clinical studies on a local level while maintaining high-quality standards and regulatory compliance. Please note this role is for upcoming f

Summary of Responsibilities:Coordinate and support activities for Data Monitoring Committees (DMCs) including but not limited to timeline generation selection of DMC members coordination and review of DMC contracts charter development travel arrangements meeting organization and prepa

Summary of Responsibilities:Coordinate and support activities for Data Monitoring Committees (DMCs) including but not limited to timeline generation selection of DMC members coordination and review of DMC contracts charter development travel arrangements meeting organization and prepa

Clinical Research Manager (CRM)Location: Client Office (as assigned)Travel: Up to 25% domestic and internationalAbout the RoleAs a Clinical Research Manager youll lead and oversee local clinical trial operations ensuring regulatory and financial compliance while driving performance ac

Clinical Research Manager (CRM)Location: Client Office (as assigned)Travel: Up to 25% domestic and internationalAbout the RoleAs a Clinical Research Manager youll lead and oversee local clinical trial operations ensuring regulatory and financial compliance while driving performance ac

Job Overview:The Associate Medical Data Review Manager is an important member of the Global Medical Review Team with responsibility for execution of key Central Medical Review activities within the Central Monitoring strategy such as: Collaborate within a matrix environment communicat

Job Overview:The Associate Medical Data Review Manager is an important member of the Global Medical Review Team with responsibility for execution of key Central Medical Review activities within the Central Monitoring strategy such as: Collaborate within a matrix environment communicat

The Director of Product Engineering will lead the strategy and development of our Data Management Products. This role is pivotal in shaping innovative solutions that meet the evolving needs of our clients in the life science sector. The successful candidate will bridge the gap between

The Director of Product Engineering will lead the strategy and development of our Data Management Products. This role is pivotal in shaping innovative solutions that meet the evolving needs of our clients in the life science sector. The successful candidate will bridge the gap between

We are currently seeking experienced Cardiology Device or Electrophysiology Sr. CRAs with 5 years of monitoring experience to join our FSP team! Experience in Cardio Device is required for this role. This role will include some nationwide travel. May be open to 2 years of monitoring w

We are currently seeking experienced Cardiology Device or Electrophysiology Sr. CRAs with 5 years of monitoring experience to join our FSP team! Experience in Cardio Device is required for this role. This role will include some nationwide travel. May be open to 2 years of monitoring w

We are currently seeking experienced Oncology CRAs residing in the Central & Mid-West US 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 Operatin

We are currently seeking experienced Oncology CRAs residing in the Central & Mid-West US 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 Operatin

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