FTITA Fortrea Development Limited Filiale Italiana

Position SummaryThe Clinical Start-Up & Trial Lead (Start-Up CTL) is responsible for the strategic planning coordination and oversight of clinical trial start-up activities as well as the ongoing execution of clinical studies. This hybrid role ensures operational excellence from site

Position SummaryThe Clinical Start-Up & Trial Lead (Start-Up CTL) is responsible for the strategic planning coordination and oversight of clinical trial start-up activities as well as the ongoing execution of clinical studies. This hybrid role ensures operational excellence from site

Join Our Team and Shape the Future of Clinical Research!At Fortrea we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist you will play a critical role in negotiating and managing site agreements confide

Join Our Team and Shape the Future of Clinical Research!At Fortrea we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist you will play a critical role in negotiating and managing site agreements confide

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

Position SummaryThe Clinical Start-Up & Trial Lead (Start-Up CTL) is responsible for the strategic planning coordination and oversight of clinical trial start-up activities as well as the ongoing execution of clinical studies. This hybrid role ensures operational excellence from site

Position SummaryThe Clinical Start-Up & Trial Lead (Start-Up CTL) is responsible for the strategic planning coordination and oversight of clinical trial start-up activities as well as the ongoing execution of clinical studies. This hybrid role ensures operational excellence from site

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.As an On Call Clinical Research Technician you will perform practical / administrative activities of clinical trials in Clinical Pharmacology in line wi

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.As an On Call Clinical Research Technician you will perform practical / administrative activities of clinical trials in Clinical Pharmacology in line wi

Job Overview:Accountable for the execution and oversight for the delivery of all services within an FSP model in line with the current Clinical Service Agreement (CSA). Responsible to ensure high quality performance for optimal service delivery. Responsible for providing instructions

Job Overview:Accountable for the execution and oversight for the delivery of all services within an FSP model in line with the current Clinical Service Agreement (CSA). Responsible to ensure high quality performance for optimal service delivery. Responsible for providing instructions

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

Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study to ensure EC/IRB/Third body/Regulatory Authority and any other local applications

Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study to ensure EC/IRB/Third body/Regulatory Authority and any other local applications

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

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

Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study to ensure EC/IRB/Third body/Regulatory Authority and any other local applications

Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study to ensure EC/IRB/Third body/Regulatory Authority and any other local applications

The Product Owner has a key role in providing data-driven insights that inform product decisions. They work intimately with the product team including developers designers and testers to help shape the products features and roadmap by conducting market and customer research gathering

The Product Owner has a key role in providing data-driven insights that inform product decisions. They work intimately with the product team including developers designers and testers to help shape the products features and roadmap by conducting market and customer research gathering

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 an Operational Quality Specialist to interact directly with our healthy volunteer participants while learning to read clinical

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 an Operational Quality Specialist to interact directly with our healthy volunteer participants while learning to read clinical

Job Overview:At times working under the direction of a Project Director the Senior Project Manager oversees and manages domestic regional and/or global projects. Responsibilities typically include developing and managing project teams communications risk scope schedule cost quality an

Job Overview:At times working under the direction of a Project Director the Senior Project Manager oversees and manages domestic regional and/or global projects. Responsibilities typically include developing and managing project teams communications risk scope schedule cost quality an

As a Senior Statistical Programmer 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 t

As a Senior Statistical Programmer 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 t

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 Nurse (RNs LPNs) and Paramedics to interact directly with our healthy volunteer participants while learning to read

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 Nurse (RNs LPNs) and Paramedics to interact directly with our healthy volunteer participants while learning to read

Summary of Responsibilities:Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites maintenance of study files conduct of pre-study and initiation visits; liaise with vendors; and other duties as assigned.Responsible for all asp

Summary of Responsibilities:Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites maintenance of study files conduct of pre-study and initiation visits; liaise with vendors; and other duties as assigned.Responsible for all asp

At Fortrea youll play a vital role in safeguarding patients by ensuring the quality and accuracy of clinical safety data. As an Assistant II PSS you will contribute to the review and processing of adverse event reports from clinical trials and marketed products helping advance medical

At Fortrea youll play a vital role in safeguarding patients by ensuring the quality and accuracy of clinical safety data. As an Assistant II PSS you will contribute to the review and processing of adverse event reports from clinical trials and marketed products helping advance medical

Summary of Responsibilities:To respond to medical information queries/product quality complaints/general queries that may be received over the telephone call email fax etc.Receive information record and report Adverse Drug Reaction in timelines (according to the regulations and to int

Summary of Responsibilities:To respond to medical information queries/product quality complaints/general queries that may be received over the telephone call email fax etc.Receive information record and report Adverse Drug Reaction in timelines (according to the regulations and to int

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