Fortrea
★ 4.5 (29 Verified Jobs)Departments hiring at Fortrea
29 Job openings at Fortrea
Clinical Budget Builder
Join Our Team and Shape the Future of Clinical Research! At Fortrea, we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget Specialist, you will play a critical role in the clinical trials budgeting process.
Contracts Spec II
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.
Clinical Research Associate II - Adelaide or Perth
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.
Sr. CRA with CAR-T experience to work traveling to US
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.
Senior Technical Designer
Job Overview: Responsibility for delivering EDC design and specifications within the scope of assigned projects to achieve project integrity and the delivery of on-time, quality data. Document and maintain contents of the standards library as required.
Apprentice - Employer Branding
India Apprentice Program: Exciting opportunity to be part of the Fortrea India Apprentice Program! As a Fortrea Apprentice, you will have the opportunity to support meaningful assignments that compliment an education in STEM+ Business and Healthcare disciplines, and are inspiring and valuable in...
HRSD Specialist I - Operations
Job Overview: Service Delivery, People Services Center contact, receives inquiries on service central and provide employee support.
Regulatory Operations Specialist I
Job Overview: - Perform various project management and regulatory affairs activities for Fortrea clients.Manage team including performance reviews, human resource issues, and assist Senior Management in assigning resources to projects as required.
Medical Librarian
Role Overview We are seeking a detail-oriented and research-savvy librarian to support our pharmacovigilance team by conducting systematic literature searches to identify safety signals, adverse drug reactions (ADRs), and emerging safety information.
Manager, EDS (External Data Specialist)
Summary of Responsibilities: - Based on forecast models, manage the resources to meet or exceed business Service Level Agreements. - Supervise, Mentor, Evaluate and aid in staff development, career development, people skills and achievement of competency standards.
Clinical Research Associate 1
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.
Clinical Research Associate 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.
Site Start-Up Specialist
Join Our Team and Drive Clinical Research Success! At Fortrea, we are committed to accelerating clinical trials and ensuring regulatory compliance.
Site Navigator II (Study Start-up Specialist) - Brisbane, Perth, Adelaide
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.
Centralized Study Spec I
Summary of Responsibilities: - Review and implementation of relevant study-specific plans that describe the required expectations for assigned tasks - Support system compliance and system data entry, as applicable - File required task-related documentation in the Electronic Trial Master File (eTMF)...
Start-up Specialist, Phase I
Our CPS team is currently seeking a Study Start Up Specialist with 2+ years of start-up experience residing with the U.S.
RAVE Programmer
Job Overview: - Assist in the development and implementation of solutions to DM service issues and concerns regarding Medidata RAVE, Oracle Inform, CRF Design, and Data Capture or imaging activities, including proactive prevention strategies.
REGULATORY AND START-UP
Summary of Responsibilities: - Draft, review, negotiate, and finalize Clinical Trial Agreements (CTAs), confidentiality agreements, amendments, and related site contract documentation.
Clinical Research Associate II, Phase I - California
Our Phase I team is currently seeking a Clinical Research Associate with 1+ years of experience. Ideal candidates would have phase I experience and reside in California.
Centralized Study Spec II
Summary of Responsibilities: - Draft, review, negotiate, and finalize Clinical Trial Agreements (CTAs), confidentiality agreements, amendments, and related site contract documentation.
Central Monitor I
Job Overview: The Central Monitoring Specialist is responsible for the execution of key Central monitoring (Site, subject and study level review as applicable) activities and in assisting the execution of several key activities.
Site Start-up Specialist - FSP
Join Our Team and Drive Clinical Research Success! At Fortrea, we are committed to accelerating clinical trials and ensuring regulatory compliance.
Lead Safety Systems Specialist
Job Overview: Assist with the overall Safety system implementation, support, configuration, and migration related activities. Responsible for providing this service to clients either as a support function to the client project groups or as stand- alone business.
Senior Safety System Specialist
Job Overview: Assist with the overall Safety system implementation, support, configuration, and migration related activities. Responsible for providing this service to clients either as a support function to the client project groups or as stand- alone business.
Clinical Research Associate II, Phase I - Florida
Our Phase I team is currently seeking a Clinical Research Associate with 1+ years of experience. Ideal candidates would have phase I experience and reside in the Florida.
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.
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.
Unblinded CRA 1
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.
Central Monitoring Associate Manager
Job Overview: Responsible for the execution of key central monitoring (site, subject and study level review as applicable) activities.
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