Fortrea

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

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 to interact directly with our healthy volunteer participants while learning to read clinical research protocols an

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 to interact directly with our healthy volunteer participants while learning to read clinical research protocols an

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 to interact directly with our healthy volunteer participants while learning to read clinical research protocols an

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 to interact directly with our healthy volunteer participants while learning to read clinical research protocols an

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

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

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

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

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

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

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

Job Overview:A key operational role within our matrix organization accountable for the clinical operational activities and performance within an assigned group of countries or delivery team with responsibilities for customer connections and commercial activity. Leading a team with ove

Job Overview:A key operational role within our matrix organization accountable for the clinical operational activities and performance within an assigned group of countries or delivery team with responsibilities for customer connections and commercial activity. Leading a team with ove

Job Overview:To coordinate with Finance and Delivery team to facilitate the data requirement of Projected and Rolled up Revenue Project level Margin Raising Invoicing Preparing Account/Project level business review decks and any ad hoc support required from delivery team in term of Ex

Job Overview:To coordinate with Finance and Delivery team to facilitate the data requirement of Projected and Rolled up Revenue Project level Margin Raising Invoicing Preparing Account/Project level business review decks and any ad hoc support required from delivery team in term of Ex

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

Be the connection between science and solutions. As a Clinical Research Associate II you will take the next step in your clinical research career supporting the successful delivery of clinical trials under the guidance of experienced colleagues. This role is suited for professionals w

Be the connection between science and solutions. As a Clinical Research Associate II you will take the next step in your clinical research career supporting the successful delivery of clinical trials under the guidance of experienced colleagues. This role is suited for professionals w

Job Overview:The Director level of Clinical Delivery Center of Excellence (CoE) is an experienced leader within the Clinical Delivery CoE they are expected to leverage their leadership competencies clinical delivery execution experience and client relationships to drive both financial

Job Overview:The Director level of Clinical Delivery Center of Excellence (CoE) is an experienced leader within the Clinical Delivery CoE they are expected to leverage their leadership competencies clinical delivery execution experience and client relationships to drive both financial

Our FSO team is seeking a Cardiology Respiratory Diabetes/Weight loss Immunology or MASH Sr. Clinical Project Manager or Project Manager II to join our growing team. This role requires 3-5 years of global project management experience. Candidates must be based in the United States. J

Our FSO team is seeking a Cardiology Respiratory Diabetes/Weight loss Immunology or MASH Sr. Clinical Project Manager or Project Manager II to join our growing team. This role requires 3-5 years of global project management experience. Candidates must be based in the United States. J

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

This role is for upcoming future opportunities that may arise at Fortrea.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

This role is for upcoming future opportunities that may arise at Fortrea.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

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 exp

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 exp

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