Fortrea

We are currently seeking experienced Cardiology Device or Electrophysiology Sr. CRAs with 3 years of monitoring experience to join our FSP team! Experience in Cardiology Device or Electrophysiology is required for this role. This role will include some nationwide travel during start u

We are currently seeking experienced Cardiology Device or Electrophysiology Sr. CRAs with 3 years of monitoring experience to join our FSP team! Experience in Cardiology Device or Electrophysiology is required for this role. This role will include some nationwide travel during start u

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 qualityinteraction 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 qualityinteraction with other departments

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

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

At Fortrea we believe in improving lives through the power of science collaboration and innovation. As a global CRO partner we support mission-driven sponsors in bringing new therapies to the patients who need them.Were now hiring a Study Start-Up Lead to join a sponsordedicated team

At Fortrea we believe in improving lives through the power of science collaboration and innovation. As a global CRO partner we support mission-driven sponsors in bringing new therapies to the patients who need them.Were now hiring a Study Start-Up Lead to join a sponsordedicated team

This role plays a key part in supporting Fortreas endtoend proposal development process for RFPs RFIs and client budget requests. You will coordinate and prepare highquality proposal deliverables by reviewing client documents identifying information gaps and collaborating across globa

This role plays a key part in supporting Fortreas endtoend proposal development process for RFPs RFIs and client budget requests. You will coordinate and prepare highquality proposal deliverables by reviewing client documents identifying information gaps and collaborating across globa

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 operate four

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 operate four

Fortreas FSP team is hiring Budget Builder & Site Contract Specialist!Home Based in USA or Canada. Must have 2 years of budget/contract negotiation experience at CRO level direct site facing experience and experience building global budget templates.As part of a global team you will

Fortreas FSP team is hiring Budget Builder & Site Contract Specialist!Home Based in USA or Canada. Must have 2 years of budget/contract negotiation experience at CRO level direct site facing experience and experience building global budget templates.As part of a global team you will

Were looking for a Delivery Enablement Associate to join our Clinical FSP this role you will provide essential operational and administrative support to ensure smooth client delivery and strong internal oversight.What youll doTrack key compliance metrics identify root causes and supp

Were looking for a Delivery Enablement Associate to join our Clinical FSP this role you will provide essential operational and administrative support to ensure smooth client delivery and strong internal oversight.What youll doTrack key compliance metrics identify root causes and supp

Lead Global Growth Inspire Teams and Shape the Future at FortreaJoin Fortrea as Our Next Executive Director of Business Development!Are you a visionary leader ready to drive innovation and growth in the life sciences industry Fortrea is seeking an exceptional Executive Director of Bus

Lead Global Growth Inspire Teams and Shape the Future at FortreaJoin Fortrea as Our Next Executive Director of Business Development!Are you a visionary leader ready to drive innovation and growth in the life sciences industry Fortrea is seeking an exceptional Executive Director of Bus

Join Our Team and Drive Clinical Research Success!At Fortrea we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist you will play a pivotal role in coordinating site start-up activities managing essential documents and ensuri

Join Our Team and Drive Clinical Research Success!At Fortrea we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist you will play a pivotal role in coordinating site start-up activities managing essential documents and ensuri

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

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

A career in Clinical Research with Fortrea: from the hospital ward to the world.If you join us you will work with some of the worlds leading pharmaceutical biotechnology and medical device companies in a vital stage of clinical development: establishing the safety tolerability and pha

A career in Clinical Research with Fortrea: from the hospital ward to the world.If you join us you will work with some of the worlds leading pharmaceutical biotechnology and medical device companies in a vital stage of clinical development: establishing the safety tolerability and pha

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 Title:Centralized study spec I Clinical InvoicingBusiness Title / Posting Title:Centralized study spec IRole Overview:The Business Operations Associate will play a critical role in managing clinical invoicing processes ensuring accuracy compliance and timely execution. This positi

Job Title:Centralized study spec I Clinical InvoicingBusiness Title / Posting Title:Centralized study spec IRole Overview:The Business Operations Associate will play a critical role in managing clinical invoicing processes ensuring accuracy compliance and timely execution. This positi

Fortrea is currently seeking an In House CRA to join our multi-sponsor team in the this home-based youll play a key part in supporting global clinical trials across all phases working closely with Clinical Trial Leaders and cross-functional teams to ensure smooth trial delivery.Locat

Fortrea is currently seeking an In House CRA to join our multi-sponsor team in the this home-based youll play a key part in supporting global clinical trials across all phases working closely with Clinical Trial Leaders and cross-functional teams to ensure smooth trial delivery.Locat

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

Were looking for a Business Operations Associate to join our Flexible Solutions this role you will provide essential operational and administrative support to ensure smooth client delivery and strong internal oversight.What youll doTrack key compliance metrics identify root causes an

Were looking for a Business Operations Associate to join our Flexible Solutions this role you will provide essential operational and administrative support to ensure smooth client delivery and strong internal oversight.What youll doTrack key compliance metrics identify root causes an

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