Full Time

Summary of Responsibilities:For Clinical Pharmacology studies perform role of Lead Biostatistician.For Clinical Pharmacology studies maintain awareness of project budgets and tasks.Assist in the preparation of Statistical Analysis Plans (including mock TFL shells) for studies under th

Summary of Responsibilities:For Clinical Pharmacology studies perform role of Lead Biostatistician.For Clinical Pharmacology studies maintain awareness of project budgets and tasks.Assist in the preparation of Statistical Analysis Plans (including mock TFL shells) for studies under th

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Full Time

Job Overview:Data Management leadership on studies and take responsibility for the development of the project documentation system set-up data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all DM activities (from study star

Job Overview:Data Management leadership on studies and take responsibility for the development of the project documentation system set-up data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all DM activities (from study star

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Job DescriptionOur FSP team is currently seeking Unblinded CRAs with 1-3 years of monitoring! Candidates must resided within the United States. 8-10 days on site per month being a mix of onsite and remote. Open to West coast Central and East Coast major hub locations. WHAT YOU WILL DO

Job DescriptionOur FSP team is currently seeking Unblinded CRAs with 1-3 years of monitoring! Candidates must resided within the United States. 8-10 days on site per month being a mix of onsite and remote. Open to West coast Central and East Coast major hub locations. WHAT YOU WILL DO

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Job Overview:This role sits at the center of Fortreas most important client relationshipspartnering closely with the Global VP of Sales & Client Services Business Unit Presidents Scientific Leadership and operational leaders to shape and execute bold global account strategies.Youll ow

Job Overview:This role sits at the center of Fortreas most important client relationshipspartnering closely with the Global VP of Sales & Client Services Business Unit Presidents Scientific Leadership and operational leaders to shape and execute bold global account strategies.Youll ow

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The Executive Director HR and Workday Platform Technology is the primary technology platform leader for Human Resourcesand Facilitiesand the enterprise platform owner for Workday. This role is accountable for the strategic leadership operational stability governance product roadmap an

The Executive Director HR and Workday Platform Technology is the primary technology platform leader for Human Resourcesand Facilitiesand the enterprise platform owner for Workday. This role is accountable for the strategic leadership operational stability governance product roadmap an

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Fortreas is hiring a Director Clinical FSP Delivery.We are seeking a strategic client leader with a proven record of growing key accounts and driving exceptional client outcomes. The ideal candidate brings strong presentation and executive communication skills extensive experience lea

Fortreas is hiring a Director Clinical FSP Delivery.We are seeking a strategic client leader with a proven record of growing key accounts and driving exceptional client outcomes. The ideal candidate brings strong presentation and executive communication skills extensive experience lea

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Sr. Manager Centralized Monitoring Risk-Based Monitoring (RBM) & Risk-Based Quality Management (RBQM) Latin AmericaAt Fortrea we are advancing clinical trials through innovative risk-based approaches and data-driven oversight. We are looking for an experienced Sr. Manager Centralized

Sr. Manager Centralized Monitoring Risk-Based Monitoring (RBM) & Risk-Based Quality Management (RBQM) Latin AmericaAt Fortrea we are advancing clinical trials through innovative risk-based approaches and data-driven oversight. We are looking for an experienced Sr. Manager Centralized

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Are you detail-oriented and passionate about supporting clinical research operationsIf so join our team in Munich as a Project Coordinator (Budget & Finance focus) where youll play a key role in enabling financial workflows across clinical studies. This is a sponsor-dedicated office-b

Are you detail-oriented and passionate about supporting clinical research operationsIf so join our team in Munich as a Project Coordinator (Budget & Finance focus) where youll play a key role in enabling financial workflows across clinical studies. This is a sponsor-dedicated office-b

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Full Time

Join our Proposal Management team as a Proposal Manager I where youll play a key role in bringing new business opportunities to life. Youll manage the end-to-end proposal processworking across teams to develop tailored high-quality responses to client requests including budgets timeli

Join our Proposal Management team as a Proposal Manager I where youll play a key role in bringing new business opportunities to life. Youll manage the end-to-end proposal processworking across teams to develop tailored high-quality responses to client requests including budgets timeli

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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 currently seeking a Paramedic I to interact directly with our healthy volunteer participants while learning to read clinical research protocols a

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 Paramedic I to interact directly with our healthy volunteer participants while learning to read clinical research protocols a

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Fortrea

Part-Time

Job Overview:The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Sr CRA II assures the impleme

Job Overview:The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Sr CRA II assures the impleme

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Full Time

Job Overview:Serve as a member of the project team with primary responsibility for all documentation requirements in support of Global EDC Solutions tasks to include receiving and logging-in and scanning contractual and validation documentation. Assist project teams with validation ta

Job Overview:Serve as a member of the project team with primary responsibility for all documentation requirements in support of Global EDC Solutions tasks to include receiving and logging-in and scanning contractual and validation documentation. Assist project teams with validation ta

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The Executive Director Clinical Platforms & Product Development is a senior technology and operations leader responsible for defining building and operationalizing Fortreas Clinical Platforms ecosystem. This role serves as the strategic and operational partner to the Vice President Cl

The Executive Director Clinical Platforms & Product Development is a senior technology and operations leader responsible for defining building and operationalizing Fortreas Clinical Platforms ecosystem. This role serves as the strategic and operational partner to the Vice President Cl

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Full Time

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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Fortreas FSP team is hiring a Clinical Trial Coordinator- Regulatory - Hybrid in Montreal Canada. Must be bilingual in French & English. Candidates with strong organizational skills attention to details and the ability to manage financial processes effectively will be particularly we

Fortreas FSP team is hiring a Clinical Trial Coordinator- Regulatory - Hybrid in Montreal Canada. Must be bilingual in French & English. Candidates with strong organizational skills attention to details and the ability to manage financial processes effectively will be particularly we

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The Executive Director Clinical Platforms & Product Development is a senior technology and operations leader responsible for defining building and operationalizing Fortreas Clinical Platforms ecosystem. This role serves as the strategic and operational partner to the Vice President Cl

The Executive Director Clinical Platforms & Product Development is a senior technology and operations leader responsible for defining building and operationalizing Fortreas Clinical Platforms ecosystem. This role serves as the strategic and operational partner to the Vice President Cl

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Full Time

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

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As a Statistical Programmer II in our sponsor-dedicated Flexible Solutions business unit you are central to the successful delivery of complex clinical trials (phases I-III) for renowned innovative and global top pharmaceutical companies. Oftentimes you will have the opportunity to le

As a Statistical Programmer II in our sponsor-dedicated Flexible Solutions business unit you are central to the successful delivery of complex clinical trials (phases I-III) for renowned innovative and global top pharmaceutical companies. Oftentimes you will have the opportunity to le

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Full Time

Job Overview:The Clinical Research Associate I MEA (CRA I MEA) 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 CRA I MEA shall reflect their experience and level of contribution w

Job Overview:The Clinical Research Associate I MEA (CRA I MEA) 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 CRA I MEA shall reflect their experience and level of contribution w

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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

Apply Now