Sofia, Sofia-City, Bulgaria · Remote OK
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…
Skills: Budget Building, Clinical Research, Negotiation, Communication, Organizational Skills
Taipei, Taiwan · On-site
Job Overview: Responsible for assisting with overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process, which may include safety data collected from clinical trial…
Skills: Pharmacovigilance, Adverse Event Processing, MedDRA Coding, Case Narrative Writing, Regulatory Reporting
Oeiras, Portugal · On-site
Job Overview: Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post ma…
Skills: Pharmacovigilance, Adverse Event Reporting, Case Processing, Medical Coding, Regulatory Reporting
Dallas, Texas, United States · Hybrid
Fortrea is hiring for Call Center Representatives to recruit volunteer participants for our Phase 1 normal healthy volunteer studies. We have full-time, part-time and on-call positions available. It may vary depending on…
Skills: Customer Service, Call Center Operations, Medical Terminology, Communication Skills, Computer Skills
Leeds, England, United Kingdom · On-site
What if your clinical operations expertise helped new medicines take their first step in human clinical trials? Start date: September 2026 Fortrea is one of the largest and longest‑established early‑stage clinical resear…
Skills: Clinical Trial Coordination, Study Set-up, Protocol Execution, GCP, ICH Guidelines
Beijing, Beijing, China · Hybrid
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 veri…
Skills: Site Monitoring, ICH GCP Guidelines, Source Data Verification, Clinical Trial Management, Regulatory Compliance
Beijing, Beijing, China · On-site
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 …
Skills: Site Monitoring, Site Management, Clinical Trial Process, Regulatory Guidelines, ICH GCP
Seoul, South Korea · On-site
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. T…
Skills: Site Monitoring, Site Management, Clinical Research, Regulatory Compliance, Case Report Forms
Maidenhead, England, United Kingdom · Remote OK
Senior Clinical Data Manager – FSP / oncology experience The Senior Clinical Data Manager role is a great opportunity to work within our sponsor dedicated department and have this unique relationship with a sponsor. You …
Skills: Clinical Data Management, Oncology, eCRF Creation, Data Cleaning, Vendor Management
Warsaw, Masovian Voivodeship, Poland · Hybrid
Are you looking to build your career in clinical research and gain hands-on experience in contracts negotiations? Join Fortrea as a Contract Specialist and support the successful delivery of global clinical trials. In th…
Skills: Contract Negotiation, Clinical Research, Site Agreements, Confidentiality Agreements, ICH-GCP Guidelines
Taipei, Taiwan · On-site
Job Overview: The statements below reflect the general responsibilities and requirements of the identified position but may not describe all the work requirements that may be inherent in the job. Summary of Responsibilit…
Skills: Business Development, Account Management, Strategic Planning, Negotiation, Client Retention
Milan, Lombardy, Italy · Remote OK
$35k–$50k/yr
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 Clinical Budget Specialist, you will play a crit…
Skills: Contract Negotiation, Clinical Research, Budget Planning, Fair Market Value Benchmarking, Grant Management Systems
Durham, California, United States · Remote OK
Job Overview: The Senior Director level of Clinical Delivery Center of Excellence (CoE) is an experienced leader within the Clinical Delivery CoE, they are expected to leverage their leadership competencies, clinical del…
Skills: Clinical Delivery, Project Management, Financial Stewardship, Client Relationship Management, Risk Management
Guangzhou City, Guangdong Province, China · Hybrid
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 veri…
Skills: Clinical Monitoring, ICH GCP Guidelines, Site Management, Source Data Verification, eCRF Review
Beijing, Beijing, China · Hybrid
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 veri…
Skills: Site Monitoring, ICH GCP Guidelines, Source Data Verification, Clinical Trial Management, Regulatory Compliance
Bengaluru, Karnataka, India · Remote OK
Job Overview: Collaborate with peers across the organization to achieve client-centric delivery in a matrix organization. Collaboration across all stakeholders within Site Readiness. Oversight and accountability of Regul…
Skills: Regulatory Affairs, Submission Strategy, Clinical Trial Information System (CTIS), EU CTR, Project Management
Bengaluru, Karnataka, India · Remote OK
The Manager, Business Intelligence leads and develops a team of Commercial analysts responsible for delivering high-quality reporting, dashboards, and data-driven insights that support business decision-making. This role…
Skills: People Leadership, Data Analysis, Project Management, Power BI, Tableau
Durham, California, United States · Remote OK
Summary of Responsibilities: Lead complex studies such as NDA submissions or complex, multi-protocol programs, potentially coordinating activities across multiple locations, providing statistical oversight, and attending…
Skills: Biostatistics, SAS, Statistical Analysis Plans, NDA Submissions, Sample Size Calculation
Bucharest, Romania · Hybrid
This may be time for you to join our innovative FSP team as a Clinical Research Associate (CRA) in Romania and be at the forefront of groundbreaking medical advancements in a variety of indications (Oncology, Neurology, …
Skills: Clinical Trial Monitoring, Site Management, Source Document Verification, Investigator Training, GCP Compliance
Ciudad de México, Mexico · Hybrid
Job Overview: Senior Site Navigators play 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 requir…
Skills: Site Activation, Regulatory Compliance, ICH/GCP Guidelines, Site Management, Contract Negotiation
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The role involves building and maintaining clinical study site budgets and negotiating rate cards for clinical trial agreements. You will partner with internal teams and site payment departments to ensure compatibility with payment systems and EDC requirements.
Candidates should have 2-4 years of experience in budget building or clinical research and a strong understanding of ICH GCP guidelines. A bachelor's degree is preferred, with a university-level law degree being highly desirable.
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. Your work will help drive the success of groundbreaking studies while ensuring compliance and efficiency.
In this role, you will be part of our FSPx team and work directly with one of our renowned key sponsor to advance the development of innovative, life-changing medications.
Key Responsibilities:
In this role, you will:
Support Country Study site budget template, parameter, and payment term building to ensure timely setup of individual site budgets.
Manage and execute assigned study site budget maintenance activities through life of study.
Negotiate directly with globally assigned sites master clinical trial agreements rate cards.
Partner with site payment department to ensure site budget and payment terms compatibility with payment systems and EDC requirements.
Partner with internal Study Startup team, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and implement processes.
Ensure standards are applied to the SB&C processes across projects, portfolios and support continuous improvement activities while developing TA-aligned strategies.
Leverage leading industry tools and data sources to provide budget and payment terms feedback aligned with parameters and fair market value guidance.
Promptly recognize and improve potential delays and escalate non-performance.
Required Qualifications:
To succeed in this role, you should have:
Bachelor’s degree (LLB, JD, BA, or BS) preferred; a university-level law degree is highly desirable (UK/EU).
Fortrea may consider equivalent relevant experience in lieu of educational requirements.
2–4 years of experience in budget building, clinical research, or a related field.
Strong understanding of ICH GCP guidelines and clinical research processes.
Excellent negotiation, communication, and organizational skills.
Ability to work independently and manage multiple priorities in a fast-paced environment.
Proficiency in Microsoft Office and tracking systems.
What We Offer:
Competitive salary and performance-based incentives.
Flexible work arrangements (remote/hybrid options).
Professional growth opportunities in a collaborative and innovative environment.
The opportunity to work on cutting-edge clinical research projects.
Ready to Make an Impact?
Take the next step in your career and join us in driving innovation in clinical research.
Apply today! Applications are reviewed on a rolling basis, don’t miss this opportunity!
Learn more about our EEO & Accommodations request here.
Bringing life-changing benefits to patients faster
Fortrea (Nasdaq: FTRE) is a leading global clinical research organization (CRO) dedicated to providing innovative clinical development solutions to the life sciences industry. With over 30 years of clinical research experience, Fortrea has evolved from Covance and Labcorp into a pureplay CRO built for biotech, biopharma, medical device and diagnostic innovators. Fortrea collaborates with both emerging and established companies to deliver agile, fit-for-purpose full service (FSO), functional service (FSP) and hybrid solutions. Fortrea provides comprehensive Phase I-IV clinical trial management, clinical pharmacology, and consulting services, backed by deep experience in more than 20 therapeutic areas. Operating in approximately 100 countries, our diverse and talented team brings scientific rigor, operational excellence, and a strong investigator site network to every trial. By combining the best of our legacy experience with forward-thinking innovation, Fortrea brings predictability to clinical trial execution and helps transform aspirations into outcomes. Together, exceptional is possible. Learn more at Fortrea.com
Offices: Research Triangle Park, NC, US
Bringing life-changing benefits to patients faster
Fortrea (Nasdaq: FTRE) is a leading global clinical research organization (CRO) dedicated to providing innovative clinical development solutions to the life sciences industry. With over 30 years of clinical research experience, Fortrea has evolved from Covance and Labcorp into a pureplay CRO built for biotech, biopharma, medical device and diagnostic innovators. Fortrea collaborates with both emerging and established companies to deliver agile, fit-for-purpose full service (FSO), functional service (FSP) and hybrid solutions. Fortrea provides comprehensive Phase I-IV clinical trial management, clinical pharmacology, and consulting services, backed by deep experience in more than 20 therapeutic areas. Operating in approximately 100 countries, our diverse and talented team brings scientific rigor, operational excellence, and a strong investigator site network to every trial. By combining the best of our legacy experience with forward-thinking innovation, Fortrea brings predictability to clinical trial execution and helps transform aspirations into outcomes. Together, exceptional is possible. Learn more at Fortrea.com
Offices: Research Triangle Park, NC, US
