Fortrea

At Fortrea we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an internshipits a launchpad for your future.As an Intern youll join a global team where curiosity motivation and fresh ideas are celebrated. Youll work on meaningful projects lea

At Fortrea we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an internshipits a launchpad for your future.As an Intern youll join a global team where curiosity motivation and fresh ideas are celebrated. Youll work on meaningful projects lea

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: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 settings (i.e. unsolicited reports). Manage and process ex

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 settings (i.e. unsolicited reports). Manage and process ex

Job Overview:Leading projects and project teams for providing programming and analysis support for Real World Evidence projects for Fortrea clients. Having good understanding of the various sources on Real World Data to be used in the analysis. Training and Mentoring the less experien

Job Overview:Leading projects and project teams for providing programming and analysis support for Real World Evidence projects for Fortrea clients. Having good understanding of the various sources on Real World Data to be used in the analysis. Training and Mentoring the less experien

Are you looking to grow your career in clinical researchFortrea is hiring a CRAII to join our client-dedicated team. This role is based in the North West offering an exciting opportunity to work on diverse studies while ensuring compliance with regulatory guidelines and company SOPs.W

Are you looking to grow your career in clinical researchFortrea is hiring a CRAII to join our client-dedicated team. This role is based in the North West offering an exciting opportunity to work on diverse studies while ensuring compliance with regulatory guidelines and company SOPs.W

Looking for a dynamic remote role with a global CRO Become our new Medical Contact Center Assistant!If you have educational background in healthcare speak fluent English and French and are wiling to work 3pm -12pm (CET) then this is the perfect role for you!Summary of Responsibilities

Looking for a dynamic remote role with a global CRO Become our new Medical Contact Center Assistant!If you have educational background in healthcare speak fluent English and French and are wiling to work 3pm -12pm (CET) then this is the perfect role for you!Summary of Responsibilities

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 early talent is the heartbeat of innovation. Our Early Careers program is more than an internship its a launchpad for your future.As an Intern youll join a global team where curiosity motivation and fresh ideas are celebrated. Youll work on meaningful projects le

At Fortrea we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an internship its a launchpad for your future.As an Intern youll join a global team where curiosity motivation and fresh ideas are celebrated. Youll work on meaningful projects le

As a Senior or Principal Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit you will be central to the successful delivery of complex global oncology clinical trials (Phases IIII) for some of the worlds most renowned and innovative pharmaceutical companie

As a Senior or Principal Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit you will be central to the successful delivery of complex global oncology clinical trials (Phases IIII) for some of the worlds most renowned and innovative pharmaceutical companie

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 Research Nurse (RNs LPNs) to interact directly with our healthy volunteer participants while learning to read clinical resear

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 Research Nurse (RNs LPNs) to interact directly with our healthy volunteer participants while learning to read clinical resear

Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements well invite you for an interview. If youre pre-selected our recruiter will keep in touch and let you know when the role officially opens so we can reconfirm your interest

Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements well invite you for an interview. If youre pre-selected our recruiter will keep in touch and let you know when the role officially opens so we can reconfirm your interest

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

Launch Your Career with FortreaAt Fortrea we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an internshipits a launchpad for your future.As an Internyoull join a global team where curiosity motivation and fresh ideas are celebrated. Youll w

Launch Your Career with FortreaAt Fortrea we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an internshipits a launchpad for your future.As an Internyoull join a global team where curiosity motivation and fresh ideas are celebrated. Youll w

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 Specialist you will play a critical role in the clinical trials budgeting process. Your work will help

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 Specialist you will play a critical role in the clinical trials budgeting process. Your work will help

Are you ready to take your expertise in clinical contracts and budgeting to the next level AtFortrea we are looking for a detail-oriented and strategic professional to join our FSP team as aSite Contract Lead. In this role you will be at the forefront of clinical trial execution ensur

Are you ready to take your expertise in clinical contracts and budgeting to the next level AtFortrea we are looking for a detail-oriented and strategic professional to join our FSP team as aSite Contract Lead. In this role you will be at the forefront of clinical trial execution ensur

Are you ready to make a meaningful impact in clinical research Join our team as a Clinical Research Associate II (CRA II) in France where youll play a key role in advancing observational and registry studies. Be part of a new dynamic model with a global Project Management hub supporti

Are you ready to make a meaningful impact in clinical research Join our team as a Clinical Research Associate II (CRA II) in France where youll play a key role in advancing observational and registry studies. Be part of a new dynamic model with a global Project Management hub supporti

We are currently seeking Experienced Sr. CRAs fluent in Spanish residing in the Mid West US! Also open to hub airports with direct flights to Puerto Rico. This FSP aligned role works with IVD clinical trials. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgemen

We are currently seeking Experienced Sr. CRAs fluent in Spanish residing in the Mid West US! Also open to hub airports with direct flights to Puerto Rico. This FSP aligned role works with IVD clinical trials. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgemen

Job Overview:Assist in the development and implementation of solutions to global technical service issues and concerns regarding EDC or SAS or other proprietary software including proactive prevention strategies. Develop/validate Custom/Complex SDTM/SAS datasets/Listings/reports. Effi

Job Overview:Assist in the development and implementation of solutions to global technical service issues and concerns regarding EDC or SAS or other proprietary software including proactive prevention strategies. Develop/validate Custom/Complex SDTM/SAS datasets/Listings/reports. Effi

Summary of Responsibilities:Follow applicable departmental Standard Operating Procedures and Work Instructions.Complete required trainings according to required timelines.Administer controlled documents ensuring availability to the end user.Track and report metrics as determined by ma

Summary of Responsibilities:Follow applicable departmental Standard Operating Procedures and Work Instructions.Complete required trainings according to required timelines.Administer controlled documents ensuring availability to the end user.Track and report metrics as determined by ma