Fortrea

Come join Fortrea today as a part-time Nurse Practitioner with our Phase I site based in Madison Wisconsin. The NP - Nurse Practitioner provides clinical expertise and serves as a key knowledge resource for the clinical aspects of trials conducted within Clinical Pharmacology. This ro

Come join Fortrea today as a part-time Nurse Practitioner with our Phase I site based in Madison Wisconsin. The NP - Nurse Practitioner provides clinical expertise and serves as a key knowledge resource for the clinical aspects of trials conducted within Clinical Pharmacology. This ro

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

Looking for a permanent night shift nursing role where you can use your clinical skills enjoy a predictable schedule and benefit from enhanced earningsLocation: Drapers Yard LeedsHours: 37 hours per weekShift Pattern: Three 12-hour night shifts per week (7:30pm to 7:30am)Salary: compe

Looking for a permanent night shift nursing role where you can use your clinical skills enjoy a predictable schedule and benefit from enhanced earningsLocation: Drapers Yard LeedsHours: 37 hours per weekShift Pattern: Three 12-hour night shifts per week (7:30pm to 7:30am)Salary: compe

Job Overview:The Medical Data Review Specialist II- is a senior member of the Global Medical Data Review Team with responsibility for execution of key Central Medical Review activities and assists senior staff and Medical Monitors in the execution of their responsibilities. The Medica

Job Overview:The Medical Data Review Specialist II- is a senior member of the Global Medical Data Review Team with responsibility for execution of key Central Medical Review activities and assists senior staff and Medical Monitors in the execution of their responsibilities. The Medica

Job Overview:The Corporate Communications Manager supports Fortreas business units by developing clear engaging communications that connect employees to business priorities operational updates leadership messages and key initiatives. This role partners closely with business unit leade

Job Overview:The Corporate Communications Manager supports Fortreas business units by developing clear engaging communications that connect employees to business priorities operational updates leadership messages and key initiatives. This role partners closely with business unit leade

Job Overview:The Director Enterprise Communication develops and leads enterprise-wide communication team and strategies that advance Fortreas business priorities strengthen employee understanding and support consistent credible messaging across the organization. This role partners wit

Job Overview:The Director Enterprise Communication develops and leads enterprise-wide communication team and strategies that advance Fortreas business priorities strengthen employee understanding and support consistent credible messaging across the organization. This role partners wit

Job DescriptionFortreas FSP team is hiring an Associate Manager Clin Ops! Remote based in the US.Job Overview:Manage and develop clinical operations team consisting of Clinical Research Associates. Contribute to and oversee resource planning and assignments. Provide monitoring oversig

Job DescriptionFortreas FSP team is hiring an Associate Manager Clin Ops! Remote based in the US.Job Overview:Manage and develop clinical operations team consisting of Clinical Research Associates. Contribute to and oversee resource planning and assignments. Provide monitoring oversig

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 Technician II (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 Research Technician II (On-Call) to interact directly with our healthy volunteer participants while learning to read clinical

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

Our FSP team is currently seeking Sr. CRA 2s with 4 years of monitoring residing in the Midwest 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 situations b

Our FSP team is currently seeking Sr. CRA 2s with 4 years of monitoring residing in the Midwest 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 situations b

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