Fortrea

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

Our Phase I team is currently seeking Project Coordinator I to join their growing group! All candidates must reside in the United States. As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience Fortrea

Our Phase I team is currently seeking Project Coordinator I to join their growing group! All candidates must reside in the United States. As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience Fortrea

Fortrea is looking for an experienced Contract and Budget Lead to support our key client in EMEARole objectivesManage escalations and review of assigned site budgets and contracts to ensure timely contract execution and study startup forecasts are achieved.Support the development of c

Fortrea is looking for an experienced Contract and Budget Lead to support our key client in EMEARole objectivesManage escalations and review of assigned site budgets and contracts to ensure timely contract execution and study startup forecasts are achieved.Support the development of c

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

Are you looking to grow your career in clinical research Fortrea is hiring a CRA II/SCRA to join our dynamic FSP team. We have opportunities across the UK particularly in the Midlands offering an exciting chance to work on diverse studies while ensuring compliance with regulatory guid

Are you looking to grow your career in clinical research Fortrea is hiring a CRA II/SCRA to join our dynamic FSP team. We have opportunities across the UK particularly in the Midlands offering an exciting chance to work on diverse studies while ensuring compliance with regulatory guid

Are you looking to grow your career in clinical research Fortrea is hiring an experienced CRA to join our dynamic FSP team. We have opportunities across the UK with a particular focus on the South West offering an exciting chance to work on diverse studies while ensuring compliance wi

Are you looking to grow your career in clinical research Fortrea is hiring an experienced CRA to join our dynamic FSP team. We have opportunities across the UK with a particular focus on the South West offering an exciting chance to work on diverse studies while ensuring compliance wi

The executives we hire today will define our strategy shape our culture drive innovation and influence outcomes for thousands of employees customers and patients around the world.Were seeking an accomplished Executive Recruiter to lead the identification assessment and acquisition of

The executives we hire today will define our strategy shape our culture drive innovation and influence outcomes for thousands of employees customers and patients around the world.Were seeking an accomplished Executive Recruiter to lead the identification assessment and acquisition of

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

Fortrea 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.This is a full-tim

Fortrea 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.This is a full-tim

What if your project leadership skills helped new medicines take their first step in human clinical trialsFortrea is one of the worlds largest and longest-established early-phase clinical research organizations.From first-in-human to exploratory biomarker or complex ph1b programs our

What if your project leadership skills helped new medicines take their first step in human clinical trialsFortrea is one of the worlds largest and longest-established early-phase clinical research organizations.From first-in-human to exploratory biomarker or complex ph1b programs our

The Clinical Research Manager (CRM) leads the execution and oversight of clinical trial activities within an assigned country ensuring compliance with ICH-GCP local regulations and company quality standards. Acting as the primary country-level contact for assigned studies the CRM driv

The Clinical Research Manager (CRM) leads the execution and oversight of clinical trial activities within an assigned country ensuring compliance with ICH-GCP local regulations and company quality standards. Acting as the primary country-level contact for assigned studies the CRM driv

Manager Central Monitoring RemoteAre you a clinical research leader passionate about using data analytics and innovation to improve trial quality and patient safetyAt Fortrea were looking for a Manager Central Monitoring to lead a team of talented professionals driving Risk-Based Mon

Manager Central Monitoring RemoteAre you a clinical research leader passionate about using data analytics and innovation to improve trial quality and patient safetyAt Fortrea were looking for a Manager Central Monitoring to lead a team of talented professionals driving Risk-Based Mon

Be the connection between science and solutions. As a Clinical Research Associate you will take the next step in your clinical research career supporting the successful delivery of clinical trials under the guidance of experienced colleagues. This role is suited for professionals with

Be the connection between science and solutions. As a Clinical Research Associate you will take the next step in your clinical research career supporting the successful delivery of clinical trials under the guidance of experienced colleagues. This role is suited for professionals with

Manager Central Monitoring RemoteAre you a clinical research leader passionate about using data analytics and innovation to improve trial quality and patient safetyAt Fortrea were looking for a Manager Central Monitoring to lead a team of talented professionals driving Risk-Based Mon

Manager Central Monitoring RemoteAre you a clinical research leader passionate about using data analytics and innovation to improve trial quality and patient safetyAt Fortrea were looking for a Manager Central Monitoring to lead a team of talented professionals driving Risk-Based Mon

Be the connection between science and solutions. As a Clinical Research Associate you will take the next step in your clinical research career supporting the successful delivery of clinical trials under the guidance of experienced colleagues. This role is suited for professionals with

Be the connection between science and solutions. As a Clinical Research Associate you will take the next step in your clinical research career supporting the successful delivery of clinical trials under the guidance of experienced colleagues. This role is suited for professionals with

Job DescriptionJob Overview: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 ensuring regulatory submissi

Job DescriptionJob Overview: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 ensuring regulatory submissi

oin Our Team and Drive Clinical Research Success!AtFortrea we are committed to accelerating clinical trials and ensuring regulatory compliance. As aSite Start-Up Specialistyou will play a pivotal role in coordinating site start-up activities managing essential documents and ensuring r

oin Our Team and Drive Clinical Research Success!AtFortrea we are committed to accelerating clinical trials and ensuring regulatory compliance. As aSite Start-Up Specialistyou will play a pivotal role in coordinating site start-up activities managing essential documents and ensuring r

Summary of Responsibilities:Management of complex projects under the direction of a Project Manager/Director as assigned.Ensure site monitoring responsibility for clinical studies are conducted according to Fortrea Standard Operating Procedures (SOP) ICH Guidelines and GCP.Work closel

Summary of Responsibilities:Management of complex projects under the direction of a Project Manager/Director as assigned.Ensure site monitoring responsibility for clinical studies are conducted according to Fortrea Standard Operating Procedures (SOP) ICH Guidelines and GCP.Work closel

Job Overview:At times working under the direction of a Project Director the Senior Project Manager oversees and manages domestic regional and/or global projects. Responsibilities typically include developing and managing project teams communications risk scope schedule cost quality an

Job Overview:At times working under the direction of a Project Director the Senior Project Manager oversees and manages domestic regional and/or global projects. Responsibilities typically include developing and managing project teams communications risk scope schedule cost quality an

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 Data Monitor to interact directly with our healthy volunteer participants while learning to read clinical research p

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 Data Monitor to interact directly with our healthy volunteer participants while learning to read clinical research p