Sofia, Sofia-City, Bulgaria · On-site
At Fortrea, we believe in improving lives through the power of science, collaboration, and innovation. As a global CRO partner, we support mission-driven sponsors in bringing new therapies to the patients who need them. …
Skills: Clinical Trial Agreements, Budget Negotiation, Site Contracting, Study Start-up, Fair Market Value Guidance
São Paulo, São Paulo, Brazil · On-site
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, Pro…
Skills: Project Coordination, Clinical Project Management, Budget Tracking, Vendor Management, Risk Management
Budapest, Central Hungary, Hungary · Remote OK
Role objectives Manage escalations and review of assigned site budgets and contracts to ensure timely contract execution and study startup forecasts are achieved. Support the development of creative processes, methodolog…
Skills: Clinical Trial Agreements, Budget Negotiation, Contract Execution, Fair Market Value Guidance, Study Startup
Sofia, Sofia-City, Bulgaria · On-site
At Fortrea, we believe in improving lives through the power of science, collaboration, and innovation. As a global CRO partner, we support mission-driven sponsors in bringing new therapies to the patients who need them. …
Skills: Study Start-Up, Site Activation, Clinical Operations, Project Management, Data Forecasting
Bucharest, Romania · On-site
At Fortrea, we believe in improving lives through the power of science, collaboration, and innovation. As a global CRO partner, we support mission-driven sponsors in bringing new therapies to the patients who need them. …
Skills: Study Start-Up, Site Activation, Clinical Operations, Project Management, ICF Creation
Durham, California, United States · Remote OK
$100k–$118k/yr
Fortrea's FSP Team is hiring a TMF Lead II! Remote US. Seeking strong experience in heavy metrics reporting and KPI development. The TMF Management team is responsible for the completeness and accuracy of the Trial Maste…
Skills: TMF Management, KPI Development, Metrics Reporting, Inspection Readiness, eTMF
Maidenhead, England, United Kingdom · On-site
📍 Location: UK - Midlands 📄 Contract: 12-month fixed-term (with potential extension based on business needs) 🤝 Model: Client-dedicated role (FSP) Looking to advance your career in clinical research? Fortrea is seeking…
Skills: Site Monitoring, GCP Compliance, Clinical Trial Processes, Regulatory Guidelines, Site Management
Leeds, England, United Kingdom · On-site
What if the skills you’ve built in data entry could help bring new medicines to life? Fortrea's Clinical Research Unit in Leeds is where life-saving medicines begin their journey. You’ll be part of a team that asks one c…
Skills: Data Entry, Administration, Attention To Detail, Microsoft Outlook, Microsoft Word
Madrid, Community of Madrid, Spain · Remote OK
At Fortrea, we believe in improving lives through the power of science, collaboration, and innovation. As a global CRO partner, we support mission-driven sponsors in bringing new therapies to the patients who need them. …
Skills: Site Activation, Study Start-Up, Clinical Operations, Project Management, ICF Creation
Dallas, Texas, United States · On-site
Clinical Research Physician, Dallas Phase I Onsite Fortrea is hiring a dynamic Clinical Research Physician at our Dallas, TX Phase I site — onsite, full-time, and fully immersed in cutting-edge clinical trials. If you're…
Skills: Medical Monitoring, Clinical Trial Execution, Data Review, Case Report Forms Review, Patient Care
Guangzhou City, Guangdong Province, China · On-site
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
Bengaluru, Karnataka, India · On-site
Job Overview: Manage ‘Client’ or ‘Project’ specific PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing …
Skills: Pharmacovigilance, Project Management, Adverse Event Reporting, MedDRA Coding, Regulatory Compliance
Paris, Ile-de-France, France · On-site
Fortrea is looking for an experienced clinical operations professional to join our team as Senior Site Navigator, with a strong focus on clinical trial start‑up activities and in-house CRA responsibilities. This role is …
Skills: Clinical Trial Start-Up, EC/RA Submissions, Contract Negotiation, Budget Negotiation, In-house CRA Activities
Seoul, South Korea · Hybrid
Job Overview: The Recruitment Talent Acquisition Partner will work closely with the Line Managers to build effective sourcing approaches by identifying the availability of talent across critical talent segments. The Tale…
Skills: Talent Sourcing, Pipeline Building, Market Mapping, Candidate Attraction, Boolean Search
Daytona Beach, Florida, United States · Remote OK
Job Overview: The Director/Senior Director, Participant Recruitment & Engagement is responsible for the strategic leadership, development, and execution of participant recruitment, engagement, and retention initiatives t…
Skills: Participant Recruitment, Marketing Strategy, Clinical Trial Enrollment, Digital Marketing, Participant Engagement
Dalian, Liaoning, China · Remote OK
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 m…
Skills: Adverse Event Processing, MedDRA Coding, Safety Data Entry, Regulatory Submissions, Patient Narrative Writing
Bengaluru, Karnataka, India · Hybrid
Summary of Responsibilities:Draft, review, negotiate, and finalize Clinical Trial Agreements (CTAs), confidentiality agreements, amendments, and related site contract documentation.Coordinate with sponsors, legal teams, …
Skills: Clinical Trial Agreements, Contract Negotiation, ICH-GCP Guidelines, Stakeholder Management, Protocol Amendments
Prague, Prague, Czechia · Hybrid
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
Bengaluru, Karnataka, India · Hybrid
Summary of Responsibilities: Works with internal teams to progress quality issues in QMS. Tracks timeliness of cases in QMS. Supports teams in creation of CAPAs. Maintains strong working knowledge of QMS. Interacts with …
Skills: Quality Management System, CAPA Process, GCP, GxP, Regulatory Compliance
Durham, California, United States · Remote OK
$80k–$89k/yr
Fortrea's FSP team is hiring Budget Builder & Site Contract Specialist! Home Based in USA or Canada. Must have 2+ years of budget/contract negotiation experience at CRO level, direct site facing experience and experience…
Skills: Budget Negotiation, Contract Negotiation, Clinical Trial Agreements, Global Budget Templates, Site Facing Communication
Sofia, Sofia-City, Bulgaria • On-site
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
Manage the development, negotiation, and execution of clinical trial agreements and budgets for assigned countries. Act as an escalation point to ensure sites are ready to enroll according to the startup project plan.
Requires a bachelor's degree and at least 4 years of experience in clinical research site contracting and budgeting. Must have at least 2 years of oversight experience and strong negotiation and communication skills.
At Fortrea, we believe in improving lives through the power of science, collaboration, and innovation. As a global CRO partner, we support mission-driven sponsors in bringing new therapies to the patients who need them.
We’re now hiring a Site Budget and Contract Lead to join a sponsor‑dedicated team and drive the successful planning and activation of clinical trials. If you are passionate about accelerating study timelines, using data to guide decisions, and mentoring study start-up teams — this role offers you the opportunity to create a real impact.
Work in a collaborative, global environment with experts passionate about improving clinical research.
Influence data-driven study start-up strategies for large-scale international programs.
Play a key role in optimizing processes, bringing fresh ideas, and driving continuous improvement.
Manage escalations and review of assigned site budgets and contracts to ensure timely contract execution and study startup forecasts are achieved.
Support the development of creative processes, methodologies, data, and technologies that will ensure ongoing improvements in the service delivery
Responsible for assigned country level SB&C function to develop, negotiate, administrate and execute assigned Clinical Trial Agreements and budgets.
Oversight of assigned country budget setup including parameters development.
Partner with Study Startup, SB&C team and Clinical Operations teams as an escalation point for global budget escalations outside of budget parameters.
Leverage leading industry tools and data sources to provide budget and contract feedback aligned with company parameters and fair market value guidance.
Promptly recognize and improve potential delays providing solutions to resolve and escalate non-performance.
Manage site contracts and budgets negotiation timelines to ensure sites are "Ready To Enroll" to the Startup Project Plan.
BS degree or international equivalent
4 or more years of experience in clinical research site contracting and budgeting, including country budget build with evidence of increasing responsibility within a pharmaceutical company, CRO or relevant industry vendor.
At least 2 years of site budgeting and contracting oversight
Ability to explain data, facilitate decision making processes to be data driven.
Expertise in principles driving country/site budgeting and contracting strategies.
Excellent organizational skills, decision making, communication and negotiation skills.
Ready to make an impact?
Join Fortrea and play a key role in bringing new therapies to patients faster.
Apply today and help shape the future of clinical research.
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
