Fortrea

Job DescriptionThis is an on-call as needed position to assist in covering rotational shifts of days mids and nights and weekends office-based position in Madison WI. As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in

Job DescriptionThis is an on-call as needed position to assist in covering rotational shifts of days mids and nights and weekends office-based position in Madison WI. As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in

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

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

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

Job Overview:Data Management leadership on studies and take responsibility for the development of the project documentation system set-up data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all DM activities (from study star

Job Overview:Data Management leadership on studies and take responsibility for the development of the project documentation system set-up data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all DM activities (from study star

Were excited to announce a new opportunity to join our growing team in Australia! We are currently seeking a Clinical Research Associate II (CRA2) who is passionate about advancing clinical research and making a meaningful impact in healthcare.As a CRA2 you will play a key role in man

Were excited to announce a new opportunity to join our growing team in Australia! We are currently seeking a Clinical Research Associate II (CRA2) who is passionate about advancing clinical research and making a meaningful impact in healthcare.As a CRA2 you will play a key role in man

Fortrea is growing! For one of our client we are currently looking for a Start-Up Specialist to join our team.Responsibilities (but not only):Compile and prepare routine submission filedLiaise with internal and external vendorsPerform a review of final submission documents as applicab

Fortrea is growing! For one of our client we are currently looking for a Start-Up Specialist to join our team.Responsibilities (but not only):Compile and prepare routine submission filedLiaise with internal and external vendorsPerform a review of final submission documents as applicab

Job Overview:The Clinical Site Navigator role is a hybrid position that combines start-up and iHCRA/CRA responsibilities. Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical trial and potentially t

Job Overview:The Clinical Site Navigator role is a hybrid position that combines start-up and iHCRA/CRA responsibilities. Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical trial and potentially t

Job Overview:Serve as a member of the project team with primary responsibility for coordinating the clinical data review query generation / resolution and reconciliation activities to support the Data Management lead with the delivery of clinical data according to client quality and i

Job Overview:Serve as a member of the project team with primary responsibility for coordinating the clinical data review query generation / resolution and reconciliation activities to support the Data Management lead with the delivery of clinical data according to client quality and i

Were excited to announce a new opportunity to join our growing team in Australia! We are currently seeking a Clinical Research Associate II (CRA2) who is passionate about advancing clinical research and making a meaningful impact in healthcare.As a CRA2 you will play a key role in man

Were excited to announce a new opportunity to join our growing team in Australia! We are currently seeking a Clinical Research Associate II (CRA2) who is passionate about advancing clinical research and making a meaningful impact in healthcare.As a CRA2 you will play a key role in man

Clinical Research Nurse - Early Phase Clinical TrialsLocation: Daytona Beach FLSchedule: Full-time Rotating Shifts (2-week blocks)Predictable scheduling. Meaningful work. A chance to shape the future of medicine.As one of the largest Clinical Research Organizations in the world we ope

Clinical Research Nurse - Early Phase Clinical TrialsLocation: Daytona Beach FLSchedule: Full-time Rotating Shifts (2-week blocks)Predictable scheduling. Meaningful work. A chance to shape the future of medicine.As one of the largest Clinical Research Organizations in the world we ope

Join a dedicated highperforming startup team supporting a single key client in the delivery of UK clinical trial this role you will take ownership of countrylevel regulatory activities from initial CTA preparation through ongoing maintenance amendments and safetyrelated submissions.

Join a dedicated highperforming startup team supporting a single key client in the delivery of UK clinical trial this role you will take ownership of countrylevel regulatory activities from initial CTA preparation through ongoing maintenance amendments and safetyrelated submissions.

Job Overview:The Director Strategic Sourcing is responsible for leading the strategy design and development of a world-class strategic sourcing and category management function for one or more categories or segments within Fortreas global sourcing scope. The remit for this role includ

Job Overview:The Director Strategic Sourcing is responsible for leading the strategy design and development of a world-class strategic sourcing and category management function for one or more categories or segments within Fortreas global sourcing scope. The remit for this role includ

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:Compa

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:Compa

Job Overview:The Senior Metrics Analyst works directly with the Intelligence and Insights team and supports the work to understand interpret and provide guidance on metrics and analytics. This role will perform the majority of the data loading manipulation reporting and dashboarding w

Job Overview:The Senior Metrics Analyst works directly with the Intelligence and Insights team and supports the work to understand interpret and provide guidance on metrics and analytics. This role will perform the majority of the data loading manipulation reporting and dashboarding w

Summary of Responsibilities:Responsible for medical review of serious adverse events and adverse events of special interest fromclinical trialsin support of drug safety activities for clients.When applicable responsible for preparation and medical review of Aggregate Reports required

Summary of Responsibilities:Responsible for medical review of serious adverse events and adverse events of special interest fromclinical trialsin support of drug safety activities for clients.When applicable responsible for preparation and medical review of Aggregate Reports required

Here at Fortrea we are currently recruiting for a CRA II in Bulgaria to cover sites in Bulgaria and UK.Key ResponsibilitiesManage and monitor clinical trial sites in compliance with Fortrea SOPs ICHGCP protocol requirements and applicable regulations including prestudy initiation rout

Here at Fortrea we are currently recruiting for a CRA II in Bulgaria to cover sites in Bulgaria and UK.Key ResponsibilitiesManage and monitor clinical trial sites in compliance with Fortrea SOPs ICHGCP protocol requirements and applicable regulations including prestudy initiation rout

Job Overview:The mission of the Project Management Academy (PM Academy) is to identify and develop potential clinical project management leaders of the future. Within a face-to-face continuous learning environment Project Coordinators (PC) are the right-hand support to the Project Lea

Job Overview:The mission of the Project Management Academy (PM Academy) is to identify and develop potential clinical project management leaders of the future. Within a face-to-face continuous learning environment Project Coordinators (PC) are the right-hand support to the Project Lea

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 Director Clinical Operations to interact directly with our healthy volunteer participants while learning to read clinical res

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 Director Clinical Operations to interact directly with our healthy volunteer participants while learning to read clinical res

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

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

Summary of Responsibilities:Perform the role of the Lead Statistical Programmer.Plan execute and oversee all programming activities on a study including but not limited to resource estimation working within budget meeting timelines maximizing quality interaction with other departments

Summary of Responsibilities:Perform the role of the Lead Statistical Programmer.Plan execute and oversee all programming activities on a study including but not limited to resource estimation working within budget meeting timelines maximizing quality interaction with other departments