Fortrea

Summary of Responsibilities:Review and implementation of relevant study-specific plans that describe the required expectations for assigned tasksSupport system compliance and system data entry as applicableFile required task-related documentation in the Electronic Trial Master File (e

Summary of Responsibilities:Review and implementation of relevant study-specific plans that describe the required expectations for assigned tasksSupport system compliance and system data entry as applicableFile required task-related documentation in the Electronic Trial Master File (e

Summary of Responsibilities:Owns all aspects of the appropriate request for information (RFI) process for assigned opportunities (inclusive of managing opportunities under general supervision establishing clear timelines meeting client requirement and suggesting solutions for obstacle

Summary of Responsibilities:Owns all aspects of the appropriate request for information (RFI) process for assigned opportunities (inclusive of managing opportunities under general supervision establishing clear timelines meeting client requirement and suggesting solutions for obstacle

Company Overview: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 a

Company Overview: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 a

Job Overview:Accountable for execution and oversight of local operational clinical trial activities and has ownership oversight and impact on local regulatory and financial compliance at a country operations level at the client. The position has a significant impact on how a country c

Job Overview:Accountable for execution and oversight of local operational clinical trial activities and has ownership oversight and impact on local regulatory and financial compliance at a country operations level at the client. The position has a significant impact on how a country c

Job Overview:The Central Monitoring Specialist is responsible for the execution of key Central monitoring (Site subject and study level review as applicable) activities and in assisting the execution of several key activities. The Central Monitoring Specialist collaborates with the st

Job Overview:The Central Monitoring Specialist is responsible for the execution of key Central monitoring (Site subject and study level review as applicable) activities and in assisting the execution of several key activities. The Central Monitoring Specialist collaborates with the st

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

We are seeking a Sponsor-Dedicated experience CRA with solid monitoring experience. Oncology expertise would be a plus. If you are eager to make an impact this is your chance!This role is for upcoming future opportunities that may arise at FortreaKey Responsibilities: In this role you

We are seeking a Sponsor-Dedicated experience CRA with solid monitoring experience. Oncology expertise would be a plus. If you are eager to make an impact this is your chance!This role is for upcoming future opportunities that may arise at FortreaKey Responsibilities: In this role you

We are seeking a Sponsor-Dedicated experience CRA with solid monitoring experience. Oncology expertise would be a plus. If you are eager to make an impact this is your chance!This role is for upcoming future opportunities that may arise at FortreaKey Responsibilities: In this role you

We are seeking a Sponsor-Dedicated experience CRA with solid monitoring experience. Oncology expertise would be a plus. If you are eager to make an impact this is your chance!This role is for upcoming future opportunities that may arise at FortreaKey Responsibilities: In this role you

We are seeking a Sponsor-Dedicated experience CRA with solid monitoring experience. Oncology expertise would be a plus. If you are eager to make an impact this is your chance!This role is for upcoming future opportunities that may arise at FortreaKey Responsibilities: In this role you

We are seeking a Sponsor-Dedicated experience CRA with solid monitoring experience. Oncology expertise would be a plus. If you are eager to make an impact this is your chance!This role is for upcoming future opportunities that may arise at FortreaKey Responsibilities: In this role you

Job Overview:Lead the development and implementation of solutions to global technical services issues and concerns regarding EDC tools like Medidata RAVE or Oracle Inform or Data/Report programming or Visual Analytics tools like Spotfire or Tableau. Develop/validate Custom/Complex SAS

Job Overview:Lead the development and implementation of solutions to global technical services issues and concerns regarding EDC tools like Medidata RAVE or Oracle Inform or Data/Report programming or Visual Analytics tools like Spotfire or Tableau. Develop/validate Custom/Complex SAS

Fortreas FSP team is currently seeking two CRA II professionals to join the team in Madrid. Candidates must have at least 3 - 4 years of experience working on complex clinical trials specifically within oncology early phase and respiratory.Summary of Responsibilities:Responsible for a

Fortreas FSP team is currently seeking two CRA II professionals to join the team in Madrid. Candidates must have at least 3 - 4 years of experience working on complex clinical trials specifically within oncology early phase and respiratory.Summary of Responsibilities:Responsible for a

Fortreas FSP team is currently seeking two CRA II professionals to join the team in Madrid. Candidates must have at least 3 - 4 years of experience working on complex clinical trials specifically within oncology: early phases / lung phase I / immunology / Gastrointestinal - Prostate -

Fortreas FSP team is currently seeking two CRA II professionals to join the team in Madrid. Candidates must have at least 3 - 4 years of experience working on complex clinical trials specifically within oncology: early phases / lung phase I / immunology / Gastrointestinal - Prostate -

Fortrea is seeking a Statistical Programmer to join our team at our clinical research facility in Leeds UK. This is an office-based role supporting a diverse portfolio of Phase I clinical studies across multiple sponsors and therapeutic areas. Working in a fast-paced and collaborative

Fortrea is seeking a Statistical Programmer to join our team at our clinical research facility in Leeds UK. This is an office-based role supporting a diverse portfolio of Phase I clinical studies across multiple sponsors and therapeutic areas. Working in a fast-paced and collaborative

Job DescriptionAssociate II Patient Safety Solutions Remote Based in Canada Fortrea is currently seeking a remote based Associate II (Patient Safety Solutions) to perform clinical trial and post approval adverse event case processing. This role requires strong clinical knowledge as we

Job DescriptionAssociate II Patient Safety Solutions Remote Based in Canada Fortrea is currently seeking a remote based Associate II (Patient Safety Solutions) to perform clinical trial and post approval adverse event case processing. This role requires strong clinical knowledge as we

Job Overview:Develops and delivers reimbursement and health economics services for Fortrea clients. Serves as an expert strategic consultant and advisor for reimbursement-related projects. Key liaison between customers and healthcare providers and payers as well as governmental bodies

Job Overview:Develops and delivers reimbursement and health economics services for Fortrea clients. Serves as an expert strategic consultant and advisor for reimbursement-related projects. Key liaison between customers and healthcare providers and payers as well as governmental bodies

Job Overview:The Clinical Trial Manager I has ownership in the clinical delivery and operational oversight of clinical research trials. This role collaborates with project managers and other functional leads to deliver clinical and start-up activities within budget and contract ensuri

Job Overview:The Clinical Trial Manager I has ownership in the clinical delivery and operational oversight of clinical research trials. This role collaborates with project managers and other functional leads to deliver clinical and start-up activities within budget and contract ensuri

Job Overview:Senior Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites

Job Overview:Senior Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites

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: Comp

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: Comp

Job Overview:Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites th

Job Overview:Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites th

Job Overview:The Clinical Trial Manager II has ownership in the clinical delivery and operational oversight of clinical research trials. This role collaborates with project managers and other functional leads to deliver clinical and start-up activities within budget and contract ensur

Job Overview:The Clinical Trial Manager II has ownership in the clinical delivery and operational oversight of clinical research trials. This role collaborates with project managers and other functional leads to deliver clinical and start-up activities within budget and contract ensur