fortrea
FSP Clinical Research Associate 2 - West, Central, and South Regions - Oncology
Our FSP team is currently seeking a CRA 2 in West, Central, or South Regions with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote. WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants
FSP Clinical Research Associate 2 - West, Central, and South Regions - Oncology
Clinical Research Licensed Practical Nurse (LPN) / Paramedic, Early Phase Clinical Research - Dallas, TX
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 Licensed Practical Nurse (LPN) or a Paramedic, to lead and support our Clinical Pharmacology Start-up team in initiating
Clinical Research Licensed Practical Nurse (LPN) / Paramedic, Early Phase Clinical Research - Dallas, TX
CRA II
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities fo
Project Coordinator I
Job Overview: The mission of the Project Management Academy (PM Academy) is to identify and develop potential clinical project management leaders of the future. Within a face-to-face, continuous learning environment, Project Coordinators (PC) are the right-hand support to the Project Lead. The Proje
Project Coordinator I
Job Overview: The mission of the Project Management Academy (PM Academy) is to identify and develop potential clinical project management leaders of the future. Within a face-to-face, continuous learning environment, Project Coordinators (PC) are the right-hand support to the Project Lead. The Proje
CRA 2
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities fo
Sr. CRA I
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 assigned. Functio
CRA II - SCRA - South-West
Are you looking to take the next step in your clinical research career? Fortrea is seeking an experienced CRA II or a SCRA1 to join our growing FSP team.This is a fantastic opportunity for candidates based in the South-West region (Bristol/Bath/Swindon/Gloucester/Cheltenham/Cardiff/Exeter area), whe
Compensation Specialist
Job Overview: Provides support to the Regional Manager of Compensation, including data collection, salary surveys, job evaluation and report preparation. Assists in global processes such as compensation review cycles and ensures accuracy, confidentiality, and compliance in compensation-related activ
Clinical Research Technician, Early Phase Clinical Research - Dallas, TX
*** Please note that this role requires you have experience with taking vitals, blood draws and ECG's.*** 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 Technician, to
Clinical Research Technician, Early Phase Clinical Research - Dallas, TX
Clinical Research Associate II - Immunology / Hypertension - Barcelona
Fortrea's FSP team is currently seeking two CRA2 professionals to join the team in Barcelona. Candidates must have at least 3 - 4 years of experience working on complex clinical trials, specifically within Gynecologic Oncology or Onco - Hematology . Summary of Responsibilities: Responsible for all a
Clinical Research Associate II - Immunology / Hypertension - Barcelona
CRA II - oncology: early phases / lung phase I / immunology / GI and genitourinary cancer - Madrid
Fortrea's FSP team is currently seeking two CRA II professionals to join the team in Madrid. Candidates must have at least 3 - 4 years of experience working on complex clinical trials, specifically within oncology early phase and respiratory. Summary of Responsibilities: Responsible for all aspects
CRA II - oncology: early phases / lung phase I / immunology / GI and genitourinary cancer - Madrid
Patient Meal Server / Madison, WI (On-Site)
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 Patient Meal Server to interact directly with our healthy volunteer participants while learning to read clinical research protocols and en
Clinical Research Licensed Practical Nurse (LPN) / Paramedic, Early Phase Clinical Research - Dallas, TX
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 Licensed Practical Nurse (LPN) or a Paramedic, to lead and support our Clinical Pharmacology Start-up team in initiating
Clinical Research Licensed Practical Nurse (LPN) / Paramedic, Early Phase Clinical Research - Dallas, TX
FSP Sr. Clinical Research Associate II - Southern California - Ophthalmology
Our FSP team is currently seeking an Oncology Sr. CRA 2 with 5+ years of monitoring residing in the Southern California area. WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergen
FSP Sr. Clinical Research Associate II - Southern California - Ophthalmology
Core CRA II (Shanghai)
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities fo
FSP CRA II(Guangzhou)
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities fo
FSP CRAI (Guangzhou)
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 aspects of
FSP CRA II (Guangzhou/Changsha/Nanning/Fuzhou/Xiamen)
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities fo
FSP CRA II (Guangzhou/Changsha/Nanning/Fuzhou/Xiamen)
FSP CRA II (Harbin, Changchun, Shenyang)
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities fo