Fortrea

Our FSO team is seeking an Ophthalmology Senior Clinical Project Manager or Clinical Project Manager II to join our growing team. This role requires 3 years of global project management experience with mandatory experience in ophthalmology. Candidates must be based in the United State

Our FSO team is seeking an Ophthalmology Senior Clinical Project Manager or Clinical Project Manager II to join our growing team. This role requires 3 years of global project management experience with mandatory experience in ophthalmology. Candidates must be based in the United State

Our FSO team is seeking an Cell & Gene Therapy Sr. Clinical Project Manager or Project Manager II to join our growing team. This role requires 3-5 years of global project management experience with mandatory experience in cell & gene. Candidates must be based in the United States. Jo

Our FSO team is seeking an Cell & Gene Therapy Sr. Clinical Project Manager or Project Manager II to join our growing team. This role requires 3-5 years of global project management experience with mandatory experience in cell & gene. Candidates must be based in the United States. Jo

Job Overview:The Inside Sales Associate role within Fortrea Consulting is responsible for generating business opportunity leads that achieve quarterly and annual goals managing inbound client interactions and supporting business development efforts across Fortreas Consulting organizat

Job Overview:The Inside Sales Associate role within Fortrea Consulting is responsible for generating business opportunity leads that achieve quarterly and annual goals managing inbound client interactions and supporting business development efforts across Fortreas Consulting organizat

Our FSO team is seeking an Cell & Gene Therapy Sr. Clinical Project Manager or Project Manager II to join our growing team. This role requires 3-5 years of global project management experience with mandatory experience in cell & gene. Candidates must be based in the United States. Jo

Our FSO team is seeking an Cell & Gene Therapy Sr. Clinical Project Manager or Project Manager II to join our growing team. This role requires 3-5 years of global project management experience with mandatory experience in cell & gene. Candidates must be based in the United States. Jo

Job Overview:The Clinical and Ancillary Supplies Services (CASS) Specialist II: Independently support the delivery of the Clinical and Ancillary supplies component of assigned studies within a region or for a simple global study. Act as contact with study team during clinical and anci

Job Overview:The Clinical and Ancillary Supplies Services (CASS) Specialist II: Independently support the delivery of the Clinical and Ancillary supplies component of assigned studies within a region or for a simple global study. Act as contact with study team during clinical and anci

Job Overview:Manages ARC review and are responsible for performing TMF review of electronic Trial Master Files (eTMF) Trial Country and Site artifacts for clinical studies in support of sponsors services contracts and internal business needs.Summary of Responsibilities:Position provid

Job Overview:Manages ARC review and are responsible for performing TMF review of electronic Trial Master Files (eTMF) Trial Country and Site artifacts for clinical studies in support of sponsors services contracts and internal business needs.Summary of Responsibilities:Position provid

Sponsor-dedicated. Full time. Remote in the UK Spain South Africa Greece Portugal or Hungary.We are on a mission to deliver solutions that bring life-changing treatments to patients faster.But we cant do it alone. We are seeking an experienced Senior Regulatory Medical Writer to lead

Sponsor-dedicated. Full time. Remote in the UK Spain South Africa Greece Portugal or Hungary.We are on a mission to deliver solutions that bring life-changing treatments to patients faster.But we cant do it alone. We are seeking an experienced Senior Regulatory Medical Writer to lead

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

Summary of Responsibilities:Perform Lead Biostatistician role on medium complexity studies providing statistical oversight and attending relevant project meetings.Perform project management activities for identified projects including resource planning timelines and milestone manageme

Summary of Responsibilities:Perform Lead Biostatistician role on medium complexity studies providing statistical oversight and attending relevant project meetings.Perform project management activities for identified projects including resource planning timelines and milestone manageme

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

Senior External Data Specialist Clinical Data Management / Vendor DataThe Senior External Data Specialist role is a great opportunity to support Clinical Data Management activities focused on external vendor and laboratory data. You will contribute to ensuring high-quality consistent

Senior External Data Specialist Clinical Data Management / Vendor DataThe Senior External Data Specialist role is a great opportunity to support Clinical Data Management activities focused on external vendor and laboratory data. You will contribute to ensuring high-quality consistent

We are seeking a results-driven sales professional to manage and grow assigned accounts while delivering against revenue targets. This role focuses on building strong client relationships developing strategic account plans and identifying new business opportunities.You will lead clien

We are seeking a results-driven sales professional to manage and grow assigned accounts while delivering against revenue targets. This role focuses on building strong client relationships developing strategic account plans and identifying new business opportunities.You will lead clien

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 Clinical Research Nurse to interact directly with our healthy volunteer participants while learning to read clinical research

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 Clinical Research Nurse to interact directly with our healthy volunteer participants while learning to read clinical research

Fortrea is seeking Clinical Trial Managers to join our team! We are seeking experienced CTLs with 3 years of experience. . Remote US or Canadian based. We are seeking candidates with either CAR T or Ophthalmology experience.Job Overview:The Clinical Trial Manager has ownership in the

Fortrea is seeking Clinical Trial Managers to join our team! We are seeking experienced CTLs with 3 years of experience. . Remote US or Canadian based. We are seeking candidates with either CAR T or Ophthalmology experience.Job Overview:The Clinical Trial Manager has ownership in the

At Fortrea our world-class Clinical Research Unit in Leeds is where life-changing medicines begin their journey. Located just minutes from the train station our 65000 ft² 100-bed facility is a cornerstone of early clinical development connecting science with real-world impact.Were lo

At Fortrea our world-class Clinical Research Unit in Leeds is where life-changing medicines begin their journey. Located just minutes from the train station our 65000 ft² 100-bed facility is a cornerstone of early clinical development connecting science with real-world impact.Were lo

Job Overview:Site Navigator 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 thi

Job Overview:Site Navigator 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 thi

Job Overview:Performs routine laboratory sample processingSummary of Responsibilities:Follows the laboratory procedures for specimen handling and processing.Operates laboratory equipment.Recognizes deviations from expected results and follows up appropriately.Processes and ships PK sa

Job Overview:Performs routine laboratory sample processingSummary of Responsibilities:Follows the laboratory procedures for specimen handling and processing.Operates laboratory equipment.Recognizes deviations from expected results and follows up appropriately.Processes and ships PK sa

We are looking for an experienced Centralized Clinical Team Lead I / Centralized Clinical Team Lead II to oversee and drive performance within our Central Monitoring team ensuring high-quality data review and efficient study oversight.Main ResponsibilitiesLead mentor and develop a tea

We are looking for an experienced Centralized Clinical Team Lead I / Centralized Clinical Team Lead II to oversee and drive performance within our Central Monitoring team ensuring high-quality data review and efficient study oversight.Main ResponsibilitiesLead mentor and develop a tea

Summary of Responsibilities:Management of complex projects under the direction of a Project Manager/Director as assigned.Ensure site monitoring responsibility for clinical studies are conducted according to Fortrea Standard Operating Procedures (SOP) ICH Guidelines and GCP.Work closel

Summary of Responsibilities:Management of complex projects under the direction of a Project Manager/Director as assigned.Ensure site monitoring responsibility for clinical studies are conducted according to Fortrea Standard Operating Procedures (SOP) ICH Guidelines and GCP.Work closel

Senior Clinical Data Manager fully home-basedJoining Fortreas Clinical Data Management sponsor dedicated team will offer a rewarding career a chance to work in an energetic & team-oriented workplace and exposure within a world-leading team. With the support of exceptional people from

Senior Clinical Data Manager fully home-basedJoining Fortreas Clinical Data Management sponsor dedicated team will offer a rewarding career a chance to work in an energetic & team-oriented workplace and exposure within a world-leading team. With the support of exceptional people from