fortrea

Main 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 for clin

Summary of Responsibilities: Based on forecast models, manage the resources to meet or exceed business Service Level Agreements. Supervise, Mentor, Evaluate and aid in staff development, career development, people skills and achievement of competency standards. Oversee EDC User account activations,

Join Fortrea’s mission to transform clinical trials and improve patient outcomes. As a Study Start Up Site Navigator I in Germany or Austria, you’ll support site activation activities and help ensure smooth collaboration between study teams and clinical sites. Key Responsibilities Assist with initia

We are currently seeking an experienced Clinical Trial Manager to join our Phase I team! Homebased within the US or Canada Or Mexico 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

Operating in approximately 100 countries, our diverse and talented team brings scientific rigor, operational excellence, and a strong investigator site network to every trial. By combining the best of our legacy experience with forward-thinking innovation, Fortrea brings predictability to clinical t

****This role is within a processing lab and not an analytical lab.**** As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US. We are currently seeking a Lab Technician to interact directly with our healthy volunteer par

Fortrea is seeking Clinical Team Leads to join our FSP team! We are seeking experienced CTLs with 2+ years of experience. Prior monitoring experience desired. Remote US based. Job Overview: Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as the Clinical

Job Overview: Data Management leadership on studies and take responsibility for the development of the project documentation, system set-up, data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all DM activities (from study start-up to data

Job Overview: Data Management leadership on studies and take responsibility for the development of the project documentation, system set-up, data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all DM activities (from study start-up to data

At Fortrea, we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an internship, —it’s a launchpad for your future. As an Intern, you’ll join a global team where curiosity, motivation, and fresh ideas are celebrated. You’ll work on meaningful projects, learn

Job Overview: Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites, this role ensures s

Job Overview: Perform various project management and regulatory affairs activities for Fortrea clients.Manage team including performance reviews, human resource issues, and assist Senior Management in assigning resources to projects as required. Manage, coordinate and oversee the overall Regulatory

Role Overview We are seeking a detail-oriented and research-savvy librarian to support our pharmacovigilance team by conducting systematic literature searches to identify safety signals, adverse drug reactions (ADRs), and emerging safety information. This role is critical for ensuring compliance wit

Job Overview: Primary contact with investigative sites during study maintenance and -when assigned-, site startup activities, with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made withi

Job Overview We are seeking a highly organized and detail-oriented Senior Clinical Trial Coordinator (Finance) to support financial and site payment activities across clinical studies. This role will be responsible for managing site budgets and patient reimbursement processes, coordinating contract

Be the connection between science and solutions. As a Clinical Research Associate, you will take the next step in your clinical research career, supporting the successful delivery of clinical trials under the guidance of experienced colleagues. This role is suited for professionals with at least one

📍 London | 2–3 days onsite (hybrid) Are you a regulatory‑focused Study Start‑Up expert who thrives on ownership and compliance? We’re looking for a Study Start‑Up PM to lead country‑level submissions, approvals and site readiness for a global, client‑dedicated program. What you’ll own Oversight of e

Associate Clinical Data Manager – sponsor-dedicated - remote Joining Fortrea’s Clinical Data Management sponsor dedicated team will offer a rewarding career, a chance to work in an energetic & team-oriented workplace and exposure within a world-leading team. With the support of exceptional people fr

Job Overview: The Senior Director, Technology Engineering & Site Lead serves as the senior engineering leader for Fortrea's engineering organization, the primary Foundry leadership representative for the site, and a strategic partner to the Head of the Global Digital Foundry. This role is responsibl

The DCT Lead, Clinical Trial Configuration will work within a sponsor-dedicated model, partnering closely with sponsor stakeholders and cross-functional clinical study teams to support the implementation, delivery, and oversight of clinical technologies used across clinical trials. This role serves