Clinical Researcher Jobs

Job Description The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company policies and procedures, quality standards and

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

The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in preparing grant applications and documents (for e.g., Institutional Review Board, Grants and Contracts Office). Th

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

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

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

Current Employees: If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position, please review this tip sheet. The Department of Clinical Tra

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

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

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

The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or senior clinical research staff. This individual obtains informed consent, collects, maintains and orga

LocationST. LOUIS, MO 63110

 Scheduled Hours40 Position SummaryThe research coordinator for this position supports the study protocol related to the THRIVE study. The primary aims of this trial are to determine whether patients undergoing surgery have a superior quality of recovery after re

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

Job Overview: As a CRA, you will manage and monitor clinical trial sites to ensure patient safety, data integrity, protocol compliance, and successful study delivery in accordance with ICH-GCP, local regulatory requirements, and sponsor expectations. Key Responsibilities: Conduct site monitoring vis

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 maintaining patient

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

Als führendes globales Auftragsforschungsinstitut (CRO) mit einer Leidenschaft für wissenschaftliche Präzision und einer jahrzehntelangen Erfahrung in der klinischen Entwicklung, bietet Fortrea Kunden aus der Pharma-, Biotechnologie- und Medizintechnikbranche ein breites Spektrum an Lösungen für die

We’re excited to announce a new opportunity to join our growing team in Australia! We are currently seeking a Clinical Research Associate II (CRA2) who is passionate about advancing clinical research and making a meaningful impact in healthcare. As a CRA2, you will be allocated to a dedicated sponso

Our FSP team is currently seeking a CRA 2 in Ohio, Pennsylvania, or Virginia 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

Our FSP team is currently seeking Sr. CRA 2s with 4+ years of monitoring residing on the West Coast US! 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 emergency situations based up