Fortrea

As a Principal Biostatistician at Fortrea you will play a key role in the design analysis and delivery of complex clinical trials supporting global programs from study design through to regulatory submissions and beyond.Working within our Full Service team you will partner with multid

As a Principal Biostatistician at Fortrea you will play a key role in the design analysis and delivery of complex clinical trials supporting global programs from study design through to regulatory submissions and beyond.Working within our Full Service team you will partner with multid

We exist to bring new medicines to life. What if your administrative support expertise could help us accelerate that journeyFORTREA IN LEEDS WHERE MEDICAL BREAKTHROUGHS BEGINAt Fortrea our world-class Clinical Research Unit in Leeds sits at the heart of innovation. Just a short 7-min

We exist to bring new medicines to life. What if your administrative support expertise could help us accelerate that journeyFORTREA IN LEEDS WHERE MEDICAL BREAKTHROUGHS BEGINAt Fortrea our world-class Clinical Research Unit in Leeds sits at the heart of innovation. Just a short 7-min

Job Overview:The Director level of Clinical Delivery Center of Excellence (CoE) is an experienced leader within the Clinical Delivery CoE they are expected to leverage their leadership competencies clinical delivery execution experience and client relationships to drive both financial

Job Overview:The Director level of Clinical Delivery Center of Excellence (CoE) is an experienced leader within the Clinical Delivery CoE they are expected to leverage their leadership competencies clinical delivery execution experience and client relationships to drive both financial

Raising CRO standards for innovation and delivery to help bring life-changing treatments to patients faster.Fortrea is seeking a dedicated Europe remote based Medical Director or Senior Medical Director with deep expertise in Ophthalmology along with background in innovative therapies

Raising CRO standards for innovation and delivery to help bring life-changing treatments to patients faster.Fortrea is seeking a dedicated Europe remote based Medical Director or Senior Medical Director with deep expertise in Ophthalmology along with background in innovative therapies

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 and technology sol

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 and technology sol

Regulatory Affairs Project Manager US Remote BasedFortrea is seeing a seasoned Project Manager with experience aligned with primary work in regulatory space. This role is accountable for communicating updates and issues to the team members as well as meeting the established timelines.

Regulatory Affairs Project Manager US Remote BasedFortrea is seeing a seasoned Project Manager with experience aligned with primary work in regulatory space. This role is accountable for communicating updates and issues to the team members as well as meeting the established timelines.

Job Overview:As an Executive support Level 3 Technician you are focused on providing the highest level of customer response professional presence technical support problem-solving and personal attention to meet the demanding schedule of the executives between the Executive support you

Job Overview:As an Executive support Level 3 Technician you are focused on providing the highest level of customer response professional presence technical support problem-solving and personal attention to meet the demanding schedule of the executives between the Executive support you

Our FSP team is currently seeking Unblinded CRAs with 1-3 years of monitoring! Candidates must resided within the United States. 8-10 days on site per month being a mix of onsite and remote. Open to West coast Central and East Coast major hub locations. WHAT YOU WILL DOYou will utiliz

Our FSP team is currently seeking Unblinded CRAs with 1-3 years of monitoring! Candidates must resided within the United States. 8-10 days on site per month being a mix of onsite and remote. Open to West coast Central and East Coast major hub locations. WHAT YOU WILL DOYou will utiliz

This role is for upcoming future opportunities that may arise at Fortrea.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

This role is for upcoming future opportunities that may arise at Fortrea.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

We are seeking a detail-oriented Safety Science Specialist to support end-to-end pharmacovigilance activities for our this role you will manage adverse event (AE) reporting across clinical trials and post-market programs ensuring timely accurate and compliant delivery in line with re

We are seeking a detail-oriented Safety Science Specialist to support end-to-end pharmacovigilance activities for our this role you will manage adverse event (AE) reporting across clinical trials and post-market programs ensuring timely accurate and compliant delivery in line with re

Job Overview:Manage Client or Project specific 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) for specified projects. Manage and

Job Overview:Manage Client or Project specific 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) for specified projects. Manage and

Job Overview:Prepares and negotiates and assists in the execution and retention of site agreements confidentiality agreements letters of indemnification and other contracts for Sponsors who contract Fortrea to perform this service. Maintains and contributes to contracts tracking and s

Job Overview:Prepares and negotiates and assists in the execution and retention of site agreements confidentiality agreements letters of indemnification and other contracts for Sponsors who contract Fortrea to perform this service. Maintains and contributes to contracts tracking and s

Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study to ensure EC/IRB/Third body/Regulatory Authority and any other local applications

Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study to ensure EC/IRB/Third body/Regulatory Authority and any other local applications

Job Overview:Manage Client or Project specific 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) for specified projects. Manage and

Job Overview:Manage Client or Project specific 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) for specified projects. Manage and

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

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 Lab Sample Coordinator (On-Call) to interact directly with our healthy volunteer participants while learning to read clinical

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 Lab Sample Coordinator (On-Call) to interact directly with our healthy volunteer participants while learning to read clinical

Our FSP team is currently seeking an CTA to join our growing team! Candidates must be within the United States.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

Our FSP team is currently seeking an CTA to join our growing team! Candidates must be within the United States.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

Job Overview:The Director level of Clinical Delivery Center of Excellence (CoE) is an experienced leader within the Clinical Delivery CoE they are expected to leverage their leadership competencies clinical delivery execution experience and client relationships to drive both financial

Job Overview:The Director level of Clinical Delivery Center of Excellence (CoE) is an experienced leader within the Clinical Delivery CoE they are expected to leverage their leadership competencies clinical delivery execution experience and client relationships to drive both financial

Our FSO team is seeking an Cell & Gene Therapy Clinical Project Manager to join our growing team. This role requires 2 years of global project management experience with experience in cell & gene therapy. Candidates must be based in the United States.Job Overview:Project Managers own

Our FSO team is seeking an Cell & Gene Therapy Clinical Project Manager to join our growing team. This role requires 2 years of global project management experience with experience in cell & gene therapy. Candidates must be based in the United States.Job Overview:Project Managers own

Join Fortreas Talent Acquisition Team! We are hiring a Senior Talent Acquisition Partner this role is hybrid (1-2 days per week) based out of our Durham NC office.Summary of Responsibilities:Subject Matter Expert (SME) for assigned business unit: As the RTA partner to a specific busin

Join Fortreas Talent Acquisition Team! We are hiring a Senior Talent Acquisition Partner this role is hybrid (1-2 days per week) based out of our Durham NC office.Summary of Responsibilities:Subject Matter Expert (SME) for assigned business unit: As the RTA partner to a specific busin