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Onsite clinical research physician in Madison, WI leading Phase I trials, overseeing healthy volunteers, and ensuring protocol compliance with medical oversight and regulatory coordination.
Summary of Responsibilities: • Maintain working knowledge of benefits practices and statutory requirements across selected EMEA countries, including pension, insured benefits, leave, wellness and locally mandated…
The Clinical Research Manager (CRM) leads the execution and oversight of clinical trial activities within an assigned country, ensuring compliance with ICH-GCP, local regulations, and company quality standards. Acting…
Oversee full-cycle early-phase clinical trials for new medicines, leading global teams to deliver Phase Ib studies and ensure compliance with safety and regulatory standards.
Job Overview: Global HR Business Partner and primary HR advisor to senior functional leaders and/or direct reports to C-suite executives supporting complex global functions (IT, Finance and other groups) and…
Oversee oncology clinical trials for a CRO, managing budgets, timelines, and cross-functional teams to ensure regulatory compliance and patient-centric delivery.
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…
Recruits clinical research professionals in Seoul by building talent pipelines, sourcing passive candidates, and mapping competitor talent markets using CRM and ATS tools.
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-,…
Our FSP team is currently seeking Unblinded CRAs with 1-3 years of monitoring! Candidates must resided within the United States. 8-10 days on site per month being a mix of onsite and remote. Open to West Coast…
Senior Clinical Data Manager – fully home-based Joining Fortrea’s Clinical Data Management sponsor dedicated team will offer a rewarding career, a chance to work in an energetic & team-oriented workplace and…
Are you passionate about clinical trial budgeting, financial strategy, and delivering accurate, competitive study cost estimates? Join Fortrea as an Investigator Grants Manager / Clinical Trial Costing Manager and play…
Role Overview The Workday Security Lead/Senior Manager is responsible for driving the design, governance, and continuous enhancement of the Workday security framework across the enterprise. This role ensures secure,…
Are you detail-oriented and passionate about supporting clinical research operations? If so, join our team in Munich as a Project Coordinator (Budget & Finance focus) , where you’ll play a key role in enabling…
Job Overview: In this role, you’ll drive revenue growth across strategic and complex accounts through proactive outreach, smart networking, and sharp commercial execution. You’ll be the person who connects the…
Location: Poland (Home-Based) At Fortrea, we are advancing clinical trials through innovative, risk-based approaches and data-driven oversight. We are looking for an experienced Manager, Centralized & Risk-Based…
Summary of Responsibilities Provides executive leadership for Quality Assurance (QA) and Regulatory Compliance within the Clinical Pharmacology Services (CPS) business unit, ensuring a robust, risk-based, and…
Fortrea is expanding its Clinical Data Management team and we're looking for a Manager, Clinical Data Management (CDM) to join our organization. This is an exciting opportunity to lead and develop high-performing…
We are seeking a highly skilled Workday Configuration Lead with deep expertise in Procure-to-Pay (P2P) modules. This senior-level individual contributor role will be responsible for designing, building, testing, and…
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.…
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