FTITA Fortrea Development Limited Filiale Italiana

HR Service Delivery Manager is primarily responsible for managing the work of the HR Service Delivery staff and allocating resources based on nature and volume of work. This includes participating in decisions regarding new work that Service Delivery will take ownership of and incorpo

HR Service Delivery Manager is primarily responsible for managing the work of the HR Service Delivery staff and allocating resources based on nature and volume of work. This includes participating in decisions regarding new work that Service Delivery will take ownership of and incorpo

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

What if your PK expertise was the reason a new drug reached patients fasterBefore a drug becomes a treatment it comes through us. Fortrea is one of the largest early-stage clinical research organizations in the world. Our Clinical Pharmacology team delivers the PK and safety insights

What if your PK expertise was the reason a new drug reached patients fasterBefore a drug becomes a treatment it comes through us. Fortrea is one of the largest early-stage clinical research organizations in the world. Our Clinical Pharmacology team delivers the PK and safety insights

Job Overview:The In-House Clinical Research Associate (IHCRA I) 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 IHCRA I shall reflect their experience and level of contribution wh

Job Overview:The In-House Clinical Research Associate (IHCRA I) 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 IHCRA I shall reflect their experience and level of contribution wh

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:The Senior CRA 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 assure the implementation of project plans as assigned. F

Job Overview:The Senior CRA 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 assure the implementation of project plans as assigned. F

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:The Clinical Trial Administrator (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 CTA shall reflect their experience and level of contribution which they can mak

Job Overview:The Clinical Trial Administrator (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 CTA shall reflect their experience and level of contribution which they can mak

Summary of Responsibilities:Tracking and Progression of Quality Issue.Development and delivery of training (to operational groups).Provide advice and guidance on aspects of quality and compliance.Provide consultation to the operational team on quality issues workflow.Cross-site QA and

Summary of Responsibilities:Tracking and Progression of Quality Issue.Development and delivery of training (to operational groups).Provide advice and guidance on aspects of quality and compliance.Provide consultation to the operational team on quality issues workflow.Cross-site QA and

Job Overview:The Product Management to lead the strategy and development of our life sciences software. This role is pivotal in shaping innovative solutions that meet the evolving needs of our clients in the life science sector. The successful candidate will bridge the gap between tec

Job Overview:The Product Management to lead the strategy and development of our life sciences software. This role is pivotal in shaping innovative solutions that meet the evolving needs of our clients in the life science sector. The successful candidate will bridge the gap between tec

Job Overview:The In-House Clinical Research Associate (IHCRA I) 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 IHCRA I shall reflect their experience and level of contribution wh

Job Overview:The In-House Clinical Research Associate (IHCRA I) 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 IHCRA I shall reflect their experience and level of contribution wh

***Must be actively registered as a Pharmacy Technician in the state of Wisconsin***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 Pharmacy Technician to assist in a fast-p

***Must be actively registered as a Pharmacy Technician in the state of Wisconsin***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 Pharmacy Technician to assist in a fast-p

We are seeking a highly skilled Workday FINS (Financials) Architect to join our dynamic IT team. The ideal candidate will have extensive experience in Workday Financials and how to successfully deliver the solution within the challenges of the CRO environment. As a Workday FINS Archit

We are seeking a highly skilled Workday FINS (Financials) Architect to join our dynamic IT team. The ideal candidate will have extensive experience in Workday Financials and how to successfully deliver the solution within the challenges of the CRO environment. As a Workday FINS Archit

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

Shape the Future of Global Clinical TrialsJoin our dynamic team and lead the crucial start-up phase of impactful clinical trials with opportunities for international exposure. Youll ensure projects are delivered on time within budget and to the highest quality standards directly contr

Shape the Future of Global Clinical TrialsJoin our dynamic team and lead the crucial start-up phase of impactful clinical trials with opportunities for international exposure. Youll ensure projects are delivered on time within budget and to the highest quality standards directly contr

***Free Parking****** Please note that this position will be a straight weekend night shift (Friday Saturday & Sunday) from 6pm-6am CST. ***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 curre

***Free Parking****** Please note that this position will be a straight weekend night shift (Friday Saturday & Sunday) from 6pm-6am CST. ***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 curre

This may be time for you to join our innovative FSP team as a Clinical Research Associate (CRA) in Romania and be at the forefront of groundbreaking medical advancements in a variety of indications (Oncology Neurology Gene Therapy...).Key Responsibilities:Monitor Clinical Trials - con

This may be time for you to join our innovative FSP team as a Clinical Research Associate (CRA) in Romania and be at the forefront of groundbreaking medical advancements in a variety of indications (Oncology Neurology Gene Therapy...).Key Responsibilities:Monitor Clinical Trials - con

As an experienced Principal Biostatistician in our sponsor-dedicated Flexible Solutions business unit you are central to the successful delivery of complex clinical trials for renowned innovative and global top pharmaceutical and biotech companies.In this role you will develop and rev

As an experienced Principal Biostatistician in our sponsor-dedicated Flexible Solutions business unit you are central to the successful delivery of complex clinical trials for renowned innovative and global top pharmaceutical and biotech companies.In this role you will develop and rev

As a Lead Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit you are central to the successful delivery of complex projects for a renowned innovative and global top pharmaceutical company.You will be involved in liaising with the entire study team as need

As a Lead Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit you are central to the successful delivery of complex projects for a renowned innovative and global top pharmaceutical company.You will be involved in liaising with the entire study team as need

Job Overview:May support Lead Data Manager (LDM) with the review maintenance and update of external vendor data received from central vendor or local laboratories. Working to ensure company SOPs (or sponsor if applicable) guidelines and global standards are followed to maintain data i

Job Overview:May support Lead Data Manager (LDM) with the review maintenance and update of external vendor data received from central vendor or local laboratories. Working to ensure company SOPs (or sponsor if applicable) guidelines and global standards are followed to maintain data i