Fortrea

Job Overview:Provides medical direction for the conduct of early clinical trials. Responsible for supporting the development activities of proposed and ongoing projects in their area of expertise as well as medical monitoring assigned clinical studies.Summary of Responsibilities: Comp

Job Overview:Provides medical direction for the conduct of early clinical trials. Responsible for supporting the development activities of proposed and ongoing projects in their area of expertise as well as medical monitoring assigned clinical studies.Summary of Responsibilities: Comp

Job Overview:Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites th

Job Overview:Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites th

Job Overview:The Clinical Trial Manager II has ownership in the clinical delivery and operational oversight of clinical research trials. This role collaborates with project managers and other functional leads to deliver clinical and start-up activities within budget and contract ensur

Job Overview:The Clinical Trial Manager II has ownership in the clinical delivery and operational oversight of clinical research trials. This role collaborates with project managers and other functional leads to deliver clinical and start-up activities within budget and contract ensur

Fortrea is seeking Clinical Trial Manager to join our FSP team! We are seeking experienced CTLs with 1 years of experience. We are seeking candidates with Oncology experience. Open to very strong Lead CRAs.Remote within the US. Job Overview:The Clinical Trial Manager I has ownership i

Fortrea is seeking Clinical Trial Manager to join our FSP team! We are seeking experienced CTLs with 1 years of experience. We are seeking candidates with Oncology experience. Open to very strong Lead CRAs.Remote within the US. Job Overview:The Clinical Trial Manager I has ownership i

Senior Clinical Programmer Analyst Remote MexicoJoin Fortrea and work from anywhere in Mexico while contributing to global clinical trials that help bring life-changing therapies to patients worldwide.Were seeking an experienced Senior Clinical Programming & Analytics Specialist to l

Senior Clinical Programmer Analyst Remote MexicoJoin Fortrea and work from anywhere in Mexico while contributing to global clinical trials that help bring life-changing therapies to patients worldwide.Were seeking an experienced Senior Clinical Programming & Analytics Specialist to l

Fortreas FSP team is hiring a Clinical Operations Manager- 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 Operations Manager- 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 Operations Manager- 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 Operations Manager- 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

Senior Technical Designer Medidata RAVE certifiedJoin our growing team and discover your extraordinary potential by working as a Senior Technical Designer within our division working with some of our most important sponsors. The position offers a strong support network flexible worki

Senior Technical Designer Medidata RAVE certifiedJoin our growing team and discover your extraordinary potential by working as a Senior Technical Designer within our division working with some of our most important sponsors. The position offers a strong support network flexible worki

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 Manager Clinical Operations II to interact directly with our healthy volunteer participants while learning to read clinical r

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 Manager Clinical Operations II to interact directly with our healthy volunteer participants while learning to read clinical r

Job Overview:The Senior Associate Real World Data (RWD) Analyst in our Fortrea Consulting group is responsible for supporting our Real-world Evidence (RWE) services through successful delivery of complex analyses of data generated from global prospective and retrospective observationa

Job Overview:The Senior Associate Real World Data (RWD) Analyst in our Fortrea Consulting group is responsible for supporting our Real-world Evidence (RWE) services through successful delivery of complex analyses of data generated from global prospective and retrospective observationa

Senior Clinical Data Manager sponsor dedicated (home-based in Poland)Joining Fortreas Clinical Data Management sponsor dedicated team will offer a rewarding career a chance to work in an energetic & team-oriented workplace and exposure within a world-leading team. With the support of

Senior Clinical Data Manager sponsor dedicated (home-based in Poland)Joining Fortreas Clinical Data Management sponsor dedicated team will offer a rewarding career a chance to work in an energetic & team-oriented workplace and exposure within a world-leading team. With the support of

Job Overview:The Principal Consultant Senior Director within Fortrea Consulting is an experienced consultant and researcher focused on strategizing and building client relationships across a broad spectrum of consulting areas (e.g. clinical development realworld evidence (RWE) health

Job Overview:The Principal Consultant Senior Director within Fortrea Consulting is an experienced consultant and researcher focused on strategizing and building client relationships across a broad spectrum of consulting areas (e.g. clinical development realworld evidence (RWE) health

Job Overview:Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as the Clinical Project Manager (CPM) within the core project team. CTLs partner with the Project Manager and other functional leads to ensure successful delivery of the clinica

Job Overview:Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as the Clinical Project Manager (CPM) within the core project team. CTLs partner with the Project Manager and other functional leads to ensure successful delivery of the clinica

Job Overview:Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as the Clinical Project Manager (CPM) within the core project team. CTLs partner with the Project Manager and other functional leads to ensure successful delivery of the clinica

Job Overview:Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as the Clinical Project Manager (CPM) within the core project team. CTLs partner with the Project Manager and other functional leads to ensure successful delivery of the clinica

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: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

At Fortrea we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist you will play a pivotal role in coordinating site start-up activities managing essential documents and ensuring regulatory submissions are completed efficientl

At Fortrea we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist you will play a pivotal role in coordinating site start-up activities managing essential documents and ensuring regulatory submissions are completed efficientl

Job Overview:Service Delivery People Services Center contact receives inquiries on service central and provide employee support. Performs workload fulfillment for Service Delivery activities (e.g. HR invoices offer administration and employee services) and enters information into admi

Job Overview:Service Delivery People Services Center contact receives inquiries on service central and provide employee support. Performs workload fulfillment for Service Delivery activities (e.g. HR invoices offer administration and employee services) and enters information into admi

Job Overview:Responsible for creation/revision/compilation/approval of Specifications/Documents for submission by Fortrea clients to US EU Japan and ROW health authorities and oversight of the same as applicable.Summary of Responsibilities:These statements are intended to describe the

Job Overview:Responsible for creation/revision/compilation/approval of Specifications/Documents for submission by Fortrea clients to US EU Japan and ROW health authorities and oversight of the same as applicable.Summary of Responsibilities:These statements are intended to describe the

Job Overview:Responsible for creation/revision/compilation/approval of Specifications/Documents for submission by Fortrea clients to US EU Japan and ROW health authorities and oversight of the same as applicable.Summary of Responsibilities:These statements are intended to describe the

Job Overview:Responsible for creation/revision/compilation/approval of Specifications/Documents for submission by Fortrea clients to US EU Japan and ROW health authorities and oversight of the same as applicable.Summary of Responsibilities:These statements are intended to describe the