About FTITA Fortrea Development Limited Filiale Italiana
26 Job openings in Fortrea
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 More...
Job Overview:Responsible for managing grant payments on assigned studies in accordance with the site agreement standard processes. Assist leadership in the development of standard processes and training for the Grant Payment team. Act as a Subject Matter Expert for grant payments for More...
Job DescriptionFortrea is currently seeking an Associate Medical Manager - MD / DO (Patient Safety Solutions) to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment.Thi More...
Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans as assigne More...
Senior Clinical Trial Assistant / Clinical Research Coordinator
Job Overview:The Senior Clinical Trial Assistant (Sr. CTA) 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 Sr. CTA shall reflect their experience and the level of contribution whi More...
Fortrea - People with Disabilities (PwD) Talent PoolFortrea is committed to building a diverse and inclusive workforce where everyone feels valued and has the opportunity to thrive. We believe that a variety of perspectives and experiences makes us stronger and enables us to better se More...
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 More...
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 More...
Summary of Responsibilities:Perform contract management tasks on medium complexity projects as assigned.Serve as contract management lead for strategic accounts as assigned.Independently develop and review Agreements including Master Services Agreements (Fortrea multi-unit single unit More...
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 More...
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 More...
Core Icf Developer/writer And Reviewer (centralized Role)
Tasks:Responsible for developing reviewing finalizing and maintaining clinical trial documents such as informed consent forms.Applies knowledge of GCP Guidelines regulatory requirements regulatory framework of privacy standards and biological samples standards therapeutic area(s) and More...
Tasks:Responsible for developing reviewing finalizing and maintaining clinical trial documents such as informed consent forms.Applies knowledge of GCP Guidelines regulatory requirements regulatory framework of privacy standards and biological samples standards therapeutic area(s) and More...
Clinical Research Associate Ii: Bring Your Career To Life At Fortrea!
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 More...
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 More...
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 More...
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 More...
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 More...
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 and technology solutions across m More...
Fortrea is looking for Senior and Principal Biostatisticians to join our sponsor dedicated teamAs a Senior Biostatistician at Fortrea you will play a crucial role in the design analysis and interpretation of clinical trials directly impacting the development of innovative therapies an More...
