FTITA Fortrea Development Limited Filiale Italiana

Are you an experienced sales professional ready to take your career to the next level Were searching for a dynamic individual with direct sales or relevant experience specifically selling services in the field of pharmacology. If you excel at connecting with mid-level and executive de

Are you an experienced sales professional ready to take your career to the next level Were searching for a dynamic individual with direct sales or relevant experience specifically selling services in the field of pharmacology. If you excel at connecting with mid-level and executive de

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: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

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

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 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

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

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

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: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

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

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

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

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

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 Screening Coordinator to coordinate compile and provide data to assist in recruiting screening and determining eligibility of

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 Screening Coordinator to coordinate compile and provide data to assist in recruiting screening and determining eligibility of

What if your pharmaceutical assistant skills are what we need to make new drugs safer for patientsFortreas cutting-edge Clinical Research Unit in Leeds is the crown jewel of our global operations. Dedicated to Phase I clinical trials this 65000 ft facility is where life-saving medicin

What if your pharmaceutical assistant skills are what we need to make new drugs safer for patientsFortreas cutting-edge Clinical Research Unit in Leeds is the crown jewel of our global operations. Dedicated to Phase I clinical trials this 65000 ft facility is where life-saving medicin

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

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

Job Overview:The Associate is involved in performing systematic literature reviews; conducting qualitative interviews with patients physicians and key opinion leaders; performing qualitative and quantitative analyses; and co-managing projects. The Associate assists other consultants i

Job Overview:The Associate is involved in performing systematic literature reviews; conducting qualitative interviews with patients physicians and key opinion leaders; performing qualitative and quantitative analyses; and co-managing projects. The Associate assists other consultants i

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

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 Clinical Research Nurse to interact directly with our healthy volunteer participants while learning to read clinical research

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 Clinical Research Nurse to interact directly with our healthy volunteer participants while learning to read clinical research

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:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all asp

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all asp

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

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