Fortrea

Job Overview:Primary contact with investigative sites during study maintenance and -when assigned- site startup activities with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions ar

Job Overview:Primary contact with investigative sites during study maintenance and -when assigned- site startup activities with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions ar

Job DescriptionAs 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 Research Technician II (On-Call) to interact directly with our healthy volunteer participants while learning t

Job DescriptionAs 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 Research Technician II (On-Call) to interact directly with our healthy volunteer participants while learning t

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

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:As an CRA I you will be responsible for site monitoring and study management activities to ensure compliance with study protocols ICH-GCP guidelines regulatory requirements and sponsor expectations. You will serve as the primary contact for assigned sites while maintainin

Job Overview:As an CRA I you will be responsible for site monitoring and study management activities to ensure compliance with study protocols ICH-GCP guidelines regulatory requirements and sponsor expectations. You will serve as the primary contact for assigned sites while maintainin

Job DescriptionJob 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 Cus

Job DescriptionJob 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 Cus

Full time. Remote in the UK South Africa Greece Portugal.Ready to take ownership of complex regulatory documents while working directly with some of the worlds leading pharmaceutical companiesAt Fortrea we help bring life-changing treatments to patients faster.To do that we need exper

Full time. Remote in the UK South Africa Greece Portugal.Ready to take ownership of complex regulatory documents while working directly with some of the worlds leading pharmaceutical companiesAt Fortrea we help bring life-changing treatments to patients faster.To do that we need exper

Our FSP team is currently seeking Sr. CRA 2s with 4 years of monitoring residing on the West Coast US!WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situation

Our FSP team is currently seeking Sr. CRA 2s with 4 years of monitoring residing on the West Coast US!WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situation

We are currently seeking Experienced Oncology CRAs to lead and support our Full Service Outsourcing team working with various sponsors. 1 year of independent CRO/sponsor monitoring required. CAR-T desired. Open to major hub locations across the US. 60-70% travel 8-10 DOS per month. WH

We are currently seeking Experienced Oncology CRAs to lead and support our Full Service Outsourcing team working with various sponsors. 1 year of independent CRO/sponsor monitoring required. CAR-T desired. Open to major hub locations across the US. 60-70% travel 8-10 DOS per month. WH

Fortrea is seeking Clinical Team Leads to join our FSP team! We are seeking experienced CTLs with 2 years of experience. Prior monitoring experience desired. Remote US based. Job Overview:Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as

Fortrea is seeking Clinical Team Leads to join our FSP team! We are seeking experienced CTLs with 2 years of experience. Prior monitoring experience desired. Remote US based. Job Overview:Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as

We are currently seeking Experienced General Medicine Sr. CRAs to lead and support our Full Service Outsourcing team. Open to major hub locations within the United States. 60-70% travel 8-10 DOS per month. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement t

We are currently seeking Experienced General Medicine Sr. CRAs to lead and support our Full Service Outsourcing team. Open to major hub locations within the United States. 60-70% travel 8-10 DOS per month. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement t

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

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