Jobs at Fortrea

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 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 Inside Sales Manager I is responsible for lead generation, managing client relationships, collaborating with business units, and achieving sales goals.

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.

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.

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 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.