fortrea

Job Overview: As a CRA, you will manage and monitor clinical trial sites to ensure patient safety, data integrity, protocol compliance, and successful study delivery in accordance with ICH-GCP, local regulatory requirements, and sponsor expectations. Key Responsibilities: Conduct site monitoring vis

Job Overview: As an CRA I, you will be responsible for site monitoring and study management activities to ensure compliance with study protocols, ICH-GCP guidelines, regulatory requirements, and sponsor expectations. You will serve as the primary contact for assigned sites while maintaining patient

Summary of Responsibilities Provides executive leadership for Quality Assurance (QA) and Regulatory Compliance within the Clinical Pharmacology Services (CPS) business unit, ensuring a robust, risk-based, and inspection-ready quality management system aligned with global regulatory expectations and

Job Overview: The Director, Global Strategic Sourcing, is responsible for leading the strategy, design and development of a world-class strategic sourcing and category management function for one or more categories or segments within Fortrea’s global sourcing scope. This leader must have the interes

The Director, Global Strategic Sourcing – IT is responsible for leading the strategy, design, and development of a world-class strategic sourcing and category management function across Fortrea’s global Information Technology spend categories. This role oversees strategic sourcing initiatives relate

Job Overview: Serve as a member of the project team with primary responsibility for all documentation requirements in support of Global EDC Solutions tasks to include receiving and logging-in and scanning contractual and validation documentation. Assist project teams with validation tasks as request

Job Overview: Responsible for the execution of key central monitoring (site, subject and study level review as applicable) activities. Collaborates within a matrix environment, communicates proactively internally and externally and across functions with key stakeholders to ensure Central Monitoring

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities fo

Als führendes globales Auftragsforschungsinstitut (CRO) mit einer Leidenschaft für wissenschaftliche Präzision und einer jahrzehntelangen Erfahrung in der klinischen Entwicklung, bietet Fortrea Kunden aus der Pharma-, Biotechnologie- und Medizintechnikbranche ein breites Spektrum an Lösungen für die

Job Overview: The Principal Consultant, Senior Director within Fortrea Consulting is an experienced consultant and researcher focused on strategizing and building client relationships across a broad spectrum of consulting areas (e.g., clinical development, real‑world evidence (RWE), health economics

We’re excited to announce a new opportunity to join our growing team in Australia! We are currently seeking a Clinical Research Associate II (CRA2) who is passionate about advancing clinical research and making a meaningful impact in healthcare. As a CRA2, you will be allocated to a dedicated sponso

We are seeking a highly skilled Workday Configuration Lead with deep expertise in Procure-to-Pay (P2P) modules. This senior-level individual contributor role will be responsible for designing, building, testing, and deploying Workday solutions that enable efficient procurement and payment processes

Summary of Responsibilities: Review and implementation of relevant study-specific plans that describe the required expectations for assigned tasks Support system compliance and system data entry, as applicable File required task-related documentation in the Electronic Trial Master File (eTMF) Review

Our FSP team is currently seeking a CRA 2 in Ohio, Pennsylvania, or Virginia with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote. WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants

Full time. Remote in the UK, South Africa, Greece, Portugal. Ready to take ownership of complex regulatory documents while working directly with some of the world's leading pharmaceutical companies? At Fortrea, we help bring life-changing treatments to patients faster. To do that, we need experience

Our FSP team is currently seeking Sr. CRA 2s with 4+ years of monitoring residing on the West Coast US! WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based up

We are currently seeking Experienced Oncology CRAs to lead and support our Full Service Outsourcing team working with various sponsors. 1+ year of independent CRO/sponsor monitoring required. CAR-T desired. Open to major hub locations across the US. 60-70% travel, 8-10 DOS per month. WHAT YOU WILL D

We are currently seeking Experienced General Medicine Sr. CRAs to lead and support our Full Service Outsourcing team. Open to major hub locations within the United States. 60-70% travel, 8-10 DOS per month. WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a

MUST be student at Universidad Panamericana OR Universidad Intercontinental Summary of Responsibilities: Ensure that all Data Management activities are conducted in compliance with relevant regulatory requirements and Good Clinical Practice. Follow applicable departmental Standard Operating Procedur

Job Overview: The Senior Director, Patient-Centered Endpoints provides strategic scientific leadership for client engagements, guiding evidence generation strategies, study design, analytical approaches, and regulatory considerations. The role oversees the delivery of complex research programs, ensu