Jobs at Fortrea

Leads complex epidemiology and real-world evidence engagements for pharmaceutical and biotechnology clients. Provides scientific oversight across study design, methodology, analysis, interpretation, and communication; advises on regulatory, payer, and health technology assessment evidence needs; manages multidisciplinary teams; supports business development, proposals, thought leadership, innovation, mentoring, and practice growth.

Leads the design, analysis, and interpretation of real-world evidence and non-interventional studies using claims, EHR, registry, and linked data. Applies advanced causal inference methods, develops statistical analysis plans, ensures regulatory alignment, manages statistical teams, mentors junior staff, supports client engagements and business development, and contributes to publications, innovation, and methodological best practices.

Monitors and manages clinical trial sites from startup through closeout, conducting site visits, training teams, reviewing source data, ensuring protocol and ICH-GCP compliance, supporting audit readiness, and resolving site-level issues. Collaborates with sponsors, vendors, and cross-functional teams while traveling to investigator sites as needed. Requires clinical monitoring experience, relevant education, strong communication skills, language fluency, and a valid driver’s license.

Supports complex clinical trials, particularly oncology studies, by coordinating project activities, maintaining essential and regulatory documentation, managing Trial Master File quality control, preparing sites and study materials, coordinating meetings and minutes, liaising with vendors, arranging study supply shipments, and providing administrative and systems support.

Perform site monitoring, initiation and closeout visits to ensure protocol compliance, patient safety, and data integrity. Support feasibility, investigator recruitment, vendor coordination, SAE reporting, and mentor junior staff while adhering to GCP and company SOPs.

Perform national site monitoring across the UK for multi‑sponsor clinical trials (oncology focus). Conduct on‑site visits (8+ days/month), apply risk‑based monitoring, and support multiple therapeutic protocols while gaining hands‑on CRO experience and career development.

Manage clinical trial site start‑up activities and act as primary site contact. Conduct site identification, feasibility, regulatory and ethics submissions, contract/budget support, remote pre‑study visits and SIV preparation. Perform in‑house/remote CRA tasks (document and CRF review, data validation) after training, maintain inspection‑ready TMF, and collaborate with CRAs and project teams to meet study milestones.

Lead eCRF design and specification writing for clinical studies using Medidata RAVE. Design and build RAVE databases, create/edit-check specifications, perform QC, maintain global library objects, support validation, lead client meetings, mentor programmers and data managers, and ensure consistency and compliance across projects.

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.

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.

Serve as the FSP subject-matter expert and strategic partner to sales and BD, develop and grow FSP business with biotech and pharma clients, support RFI/RFP responses and pricing, manage pipelines in SFDC, lead client presentations, mentor account teams, and create long-term account plans to achieve sales targets and customer retention.

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 global study start-up activities from site identification through activation. Drive site activation timelines, coordinate regulatory/IRB submissions, manage risks and stakeholders, support clinical systems implementation, and ensure ICH-GCP and local regulatory compliance.

Lead marketing for assigned therapeutic areas or services, design and execute integrated omni-channel campaigns, guide content and executive communications, partner with commercial teams, manage vendors and KPIs, support analytics and optimization, ensure regulatory/editorial compliance, and perform operational tasks to drive pipeline impact.

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

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