Jobs at Fortrea

Lead end-to-end delivery of Phase I/Phase Ib clinical pharmacology studies (healthy volunteers and patients). Serve as primary sponsor contact, manage scope/timelines/budgets, mitigate risks, lead matrix teams, ensure TMF/CTMS compliance with SOPs and ICH/GCP, and support bids, client relationships and process improvements.

Conduct site monitoring visits to ensure protocol, GCP, regulatory and SOP compliance; manage site initiation, routine monitoring and closeout; support patient safety and data integrity including SAE tracking/reporting; contribute to feasibility, investigator engagement, vendor coordination, and mentor junior team members to improve study quality.

This role involves developing and validating SAS programs for oncology clinical trials, ensuring compliance with regulatory standards and supporting data analysis and reporting.

The CRA II role involves managing complex clinical trial sites, building relationships with investigators, ensuring patient safety, and contributing to innovative studies in various therapeutic areas.

Coordinate site start-up activities, collect and submit regulatory documents (EC/IRB/RA), ensure ICH/GCP compliance, track timelines, maintain audit-ready documentation, support contracts/budgets, liaise with stakeholders, and mentor new or less-experienced colleagues to enable efficient site activation.

Negotiate, prepare, and manage site agreements, confidentiality agreements, and indemnification letters for clinical trials; ensure regulatory and SOP compliance; track contract status; collaborate with study teams, legal, and project management; maintain contract files; escalate issues and support process improvements.

Lead site identification, feasibility, and full start-up activities; manage EC/IRB/RA submissions; oversee regulatory documentation, contracts, and budgets; perform advanced in-house CRA tasks (document review, SDV/SDR, remote monitoring); ensure TMF completeness and audit readiness; mitigate risks and collaborate with cross-functional teams to meet study milestones and protect data integrity and patient safety.

Lead end-to-end clinical data management for oncology studies in a sponsor-dedicated model. Own study setup, eCRF design, data cleaning, vendor oversight, risk management, and client communication while ensuring adherence to industry standards (CDASH/SDTM) and regulatory obligations.

Lead and coordinate study start-up/site activation across countries, guide site activation specialists, develop country-specific ICFs, use data/forecasting to drive timelines, mentor team members, identify process improvements, and escalate/resolves start-up delays to achieve Ready-to-Enroll status.

Lead site budget and contract activities across assigned UK/ROI countries, negotiate Clinical Trial Agreements and site budgets, escalate and resolve complex issues, monitor timelines, support country-level budget setup, use market data to inform decisions, drive process improvements, and ensure sites are contractually and financially ready for patient enrollment.

Lead strategy and delivery of commercial and marketing technology platforms (CRM, marketing automation, proposal management, analytics). Manage product teams, budgets, vendors, integrations, data governance, and drive adoption, innovation, and business alignment.

The Associate Country Clinical Quality Manager will oversee quality compliance in clinical trials, supporting audits, inspections, and training initiatives. They will identify trends and improvement opportunities while maintaining regulatory standards.

The Senior CRA will conduct national monitoring for various therapeutic areas, focusing on oncology and other specializations, while working with multiple protocols.

As a Principal Statistical Programmer, oversee programming activities on clinical studies, mentor team members, and ensure quality outputs while interacting with cross-functional teams.

As a Senior Statistical Programmer, you will develop and validate SAS programs for clinical trial data analyses, support regulatory submissions, and lead studies, impacting patient health globally.

Lead Statistical Programmer overseeing programming activities for clinical trials, ensuring quality and adherence to standards, while mentoring team members.

The CRA II is responsible for site monitoring, ensuring compliance with protocols, managing site activities, mentoring junior CRAs, and handling Serious Adverse Events reporting.

Senior technology and operations leader responsible for defining, building, and operating Fortrea’s clinical platforms. Own product strategy, end-to-end development, regulatory-compliant deployment, PMO governance, vendor management, and commercial enablement. Lead global product, engineering, and operations teams to ensure scalable, secure, and high-quality platform delivery that supports the full clinical trial lifecycle and client-facing engagements.

The Site Navigator II manages site identification, feasibility, and start-up activities, coordinates regulatory submissions, and acts as a point of contact for investigative sites.

Manage and oversee RA, IRB/EC and Third Body submissions for assigned projects in EMEA, plan submission strategy and timelines, ensure regulatory compliance of study documents, liaise with local teams and authorities, support CTIS/EU CTR activities, manage budgets, and participate in quality, risk management, audits, and inspections.