Jobs at Fortrea

Senior pre-sales consultant driving adoption of Fortrea Intelligent Technology (FIT) across FSO, FSP, and SaaS clinical trial models. Support discovery, value/ROI storytelling, proposal strategy, competitive positioning, and customer engagements. Partner with Sales, Product, Clinical SMEs, and Marketing to win business, inform product roadmap, and enable go-to-market efforts. ~25% travel.

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.

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

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.

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.

Lead global process quality oversight by monitoring trends, audits, and escalations to identify systemic process failures. Manage end-to-end global process CAPAs, root cause analysis, and effectiveness verification. Partner with cross-functional teams to define risk-based corrective and preventive actions, maintain CAPA visibility, and support inspection-ready governance. Deliver quality insights, prepare governance updates, and support audits/inspections while promoting proactive issue management and sustainable 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.

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 Clinical Data Manager oversees clinical data management projects, provides leadership, ensures data quality, and manages vendor relationships and budgets, while driving project success through team collaboration and operational expertise.