Jobs at Fortrea

The Manager, Proposal Management will lead a team, oversee proposal processes, manage workloads, and ensure high-quality document deliveries while liaising with clients and stakeholders.

The Executive Director will lead global strategic partnerships in biopharma, manage cross-functional deal teams, influence pricing strategies, and drive revenue growth and account penetration.

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.

Drive revenue growth through strategic account management, client relationships, and business development in the biotech sector, while achieving sales targets and managing complex sales.

The Clinical Research Associate I role involves independent monitoring of clinical trials across various therapeutic areas, focusing on Oncology.

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.

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

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.

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 complex real-world evidence (RWE) studies and multi-protocol programs, develop and review SAPs, perform statistical oversight and TFL review, draft statistical protocol sections, present results, support bid defenses, and serve as Subject Matter Expert on procedural documents and initiatives.

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

The Clinical Research Manager will oversee clinical trial operations, ensuring compliance, managing timelines and budgets, and fostering vendor and investigator relationships.