Jobs at Fortrea

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.

Lead and own operational strategy for oncology clinical trials, managing scope, timeline, budget, risk, and quality. Build and mentor cross-functional global teams, drive client relationships, ensure regulatory and SOP compliance, forecast finances, manage resources and change control, and deliver presentations for business needs.

Lead end-to-end ophthalmology clinical trials, owning strategy, timelines, budget, risk, and quality. Build and mentor cross-functional teams, manage client relationships, forecast revenue, and ensure compliance with ICH/GCP and company SOPs while driving patient-centric, cost-effective delivery.

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

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.

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

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.

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.

The Statistical Programmer II leads programming activities for clinical trials, developing SAS programs, managing datasets, and ensuring quality control.

The Proposal Manager I manages the proposal process, coordinating with teams to create tailored responses to client requests while ensuring timely delivery and quality documentation.

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.

Manage UK site start-up activities for Phase I/Ib clinical trials: collect, quality‑review and compile investigator/essential documents; prepare and submit regulatory/IRB/EC/CTA/IND filings; liaise with sites, vendors and authorities; ensure ICH/GCP and local regulatory compliance; support CTIS uploads (EU), contracts/budgets tracking, mentor colleagues, and escalate risks to meet study activation timelines.

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.

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

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.