Fortrea

We are currently seeking Experienced Oncology CRAs residing in the Central & Midwest US to join our FSP team! Various openings include regional travel as well as nationwide travel options. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high

We are currently seeking Experienced Oncology CRAs residing in the Central & Midwest US to join our FSP team! Various openings include regional travel as well as nationwide travel options. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high

We are currently seeking a Clinical Quality Operations Manager!This is a full-time hybrid role based within Canada. This individual will need to be located in Canada Fluent in French and English and willing to go into the Montreal/Kirkland office twice a week.If you join us you will w

We are currently seeking a Clinical Quality Operations Manager!This is a full-time hybrid role based within Canada. This individual will need to be located in Canada Fluent in French and English and willing to go into the Montreal/Kirkland office twice a week.If you join us you will w

Fortrea is hiring a dynamic Clinical Research Physician at our Dallas TX Phase I site onsite full-time and fully immersed in cutting-edge clinical trials. If youre ready to lead with purpose grow your expertise and collaborate with a dynamic team this role could be your next big move

Fortrea is hiring a dynamic Clinical Research Physician at our Dallas TX Phase I site onsite full-time and fully immersed in cutting-edge clinical trials. If youre ready to lead with purpose grow your expertise and collaborate with a dynamic team this role could be your next big move

Job Overview:It is the responsibility of the post holder to provide all clients both internal and external with the appropriate quality of service in a safe and cost-effective manner. The individual will be expected to comply with the legal requirements of the Health and Safety at Wor

Job Overview:It is the responsibility of the post holder to provide all clients both internal and external with the appropriate quality of service in a safe and cost-effective manner. The individual will be expected to comply with the legal requirements of the Health and Safety at Wor

Job Overview:The statements below reflect the general responsibilities and requirements of the identified position but may not describe all the work requirements that may be inherent in the job.Summary of Responsibilities:Works with Global Sales and Client Services Business Unit Presi

Job Overview:The statements below reflect the general responsibilities and requirements of the identified position but may not describe all the work requirements that may be inherent in the job.Summary of Responsibilities:Works with Global Sales and Client Services Business Unit Presi

Job DescriptionThe 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

Job DescriptionThe 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

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

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 one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.Were seeking a highly motivated and detail-oriented Pharmacy Technician who thrives in a fast-paced regulated environment and is eager to grow within th

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.Were seeking a highly motivated and detail-oriented Pharmacy Technician who thrives in a fast-paced regulated environment and is eager to grow within th

Job Overview:We are seeking a detail-oriented and proactive Pharmacovigilance Associate II to support Clinical Trial and Post-Approval Case Processing Activities primarily case follow-up activities. The primary responsibility of this role is to collect and process safety data through

Job Overview:We are seeking a detail-oriented and proactive Pharmacovigilance Associate II to support Clinical Trial and Post-Approval Case Processing Activities primarily case follow-up activities. The primary responsibility of this role is to collect and process safety data through

Fortrea is currently seeking a remote based Specialist I (Patient Safety Solutions) to perform clinical trial and post approval adverse event case processing. This role requires strong clinical knowledge as well as an understanding of the US Healthcare system.This is a full-time home-

Fortrea is currently seeking a remote based Specialist I (Patient Safety Solutions) to perform clinical trial and post approval adverse event case processing. This role requires strong clinical knowledge as well as an understanding of the US Healthcare system.This is a full-time home-

We are seeking a Sponsor-Dedicated CRA with solid monitoring experience. If you are eager to make an impact this is your chance!This role is to be based in Salzburg/Linz area.Key Responsibilities: In this role you willMonitor clinical trial sites to ensure compliance with protocols GC

We are seeking a Sponsor-Dedicated CRA with solid monitoring experience. If you are eager to make an impact this is your chance!This role is to be based in Salzburg/Linz area.Key Responsibilities: In this role you willMonitor clinical trial sites to ensure compliance with protocols GC

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

Senior Analyst Real World Evidence (RWE) (Remote): This is a permanent remote opportunity that can be worked from anywhere in U.SWe are seeking a Senior Analyst Real World Evidence (RWE) (US Remote) to provide programming and analysis support for Real World Evidence projects for Fortr

Senior Analyst Real World Evidence (RWE) (Remote): This is a permanent remote opportunity that can be worked from anywhere in U.SWe are seeking a Senior Analyst Real World Evidence (RWE) (US Remote) to provide programming and analysis support for Real World Evidence projects for Fortr

Join Fortreas mission to transform clinical trials and improve patient outcomes.As a Study Start Up Site Navigator in Germany youll support site activation activities and help ensure smooth collaboration between study teams and clinical sites. This is an excellent opportunity to start

Join Fortreas mission to transform clinical trials and improve patient outcomes.As a Study Start Up Site Navigator in Germany youll support site activation activities and help ensure smooth collaboration between study teams and clinical sites. This is an excellent opportunity to start

Job Overview: The Payroll Coordinator will provide full functional payroll support for the allocated APAC payrolls although primarily home country ensuring they are processed accurately and on-time.They will ensure processing payments and reporting deadlines are met in a timely and ac

Job Overview: The Payroll Coordinator will provide full functional payroll support for the allocated APAC payrolls although primarily home country ensuring they are processed accurately and on-time.They will ensure processing payments and reporting deadlines are met in a timely and ac

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: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

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

Job Overview:Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e. unsolicited reports). Manage and process exp

Job Overview:Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e. unsolicited reports). Manage and process exp