As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience Fortrea provides pharmaceutical biotechnology and medical device customers a wide range of clinical development patient access and technology sol

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience Fortrea provides pharmaceutical biotechnology and medical device customers a wide range of clinical development patient access and technology sol

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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

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Full Time

As aProposal Manager IIwithin Fortreas Enterprise Client Solutions team youll play a pivotal role in driving the proposal process for opportunities including RFIs and RFPs. This position is ideal for someone who thrives in a fast-paced matrixed environment and enjoys collaborating acr

As aProposal Manager IIwithin Fortreas Enterprise Client Solutions team youll play a pivotal role in driving the proposal process for opportunities including RFIs and RFPs. This position is ideal for someone who thrives in a fast-paced matrixed environment and enjoys collaborating acr

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Are you detail-oriented and passionate about supporting clinical research operations Join our team in Paris as Project Assistant with Budget and Contract skills where youll play a key role in enabling regulatory or financial workflows across clinical studies. This is a sponsor-dedicat

Are you detail-oriented and passionate about supporting clinical research operations Join our team in Paris as Project Assistant with Budget and Contract skills where youll play a key role in enabling regulatory or financial workflows across clinical studies. This is a sponsor-dedicat

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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 seeking a Clinical Research Pharmacist II who will play a critical role in supporting clinical trials by ensuring the safe and compliant preparat

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 seeking a Clinical Research Pharmacist II who will play a critical role in supporting clinical trials by ensuring the safe and compliant preparat

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Job Overview:Primary contact with investigative sites during study maintenance and -when assigned- site startup activities with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions ar

Job Overview:Primary contact with investigative sites during study maintenance and -when assigned- site startup activities with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions ar

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***Must have at least 1 year of experience working within a clinical research role***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 Study Coordinator II to interact direct

***Must have at least 1 year of experience working within a clinical research role***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 Study Coordinator II to interact direct

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Full Time

Assists Proposal Managers with all aspects of the appropriate proposal process (text quote budget and/or response to Requests for Information RFIs) (i.e. collating data following up with other departments meeting minutes etc.).Responsible for managing opportunities of low complexity w

Assists Proposal Managers with all aspects of the appropriate proposal process (text quote budget and/or response to Requests for Information RFIs) (i.e. collating data following up with other departments meeting minutes etc.).Responsible for managing opportunities of low complexity w

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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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Full Time

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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Join Our Product Management Team at Fortrea! Were seeking a Product Manager with deep industry expertise and proven experience in Risk-Based Quality Management (RBQM) to lead the development of data-driven solutions that drive innovation in life sciences.In this role youll define str

Join Our Product Management Team at Fortrea! Were seeking a Product Manager with deep industry expertise and proven experience in Risk-Based Quality Management (RBQM) to lead the development of data-driven solutions that drive innovation in life sciences.In this role youll define str

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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

Apply Now
Full Time

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

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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

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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

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Full Time

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

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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

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Full Time

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

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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

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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

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