fortrea

Job Overview: Assist in the development and implementation of solutions to global technical service issues and concerns regarding EDC or SAS or other proprietary software, including proactive prevention strategies. Develop/validate Custom/Complex SDTM/SAS datasets/Listings/reports. Efficiently handl

Do you have a passion for scientific writing and clinical research? Then, join Fortrea as our next Medical Writer 1 and help ensure new medicines are safe for patients while kick-starting a global career in clinical trials. Fortrea Clinical Pharmacology Services (CPS) supports the earliest and most

Job Overview: Assist in the development and implementation of solutions to DM service issues and concerns regarding Medidata RAVE, Oracle Inform, CRF Design, and Data Capture or imaging activities, including proactive prevention strategies. Develop and maintain programs for creation of datasets as p

Job Overview: Senior 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 en

Job Overview: Site Navigators II plays 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 ensur

Job Overview: The In-House Clinical Research Associate II (IHCRA II) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the IHCRA II shall reflect their experience, and level of contribution which they

This position is within Fortrea’s Global Quality Assurance organization, responsible for providing regulatory expertise, hosting complex GCP audits and inspections, and driving global quality initiatives. This position serves as a regulatory subject matter expert (SME), supporting internal teams, cl

본 포지션은 Core Team 소속이며, 모니터링 2년 이상 경력자(SIT 연구) 분을 선호합니다. 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 traini

Senior Manager QA, Remote based in North Carolina Join Fortrea as a Senior Manager QA, External Audit, NC remote based and make an impact on the quality of clinical research by leading critical audit and inspection programs. In this highly collaborative role, you’ll influence a culture of quality, s

The QA Compliance Lead Auditor is a senior‑level role that is US remote based with preference for candidates near Durham, NC location. This position is within Fortrea’s Global Quality Assurance organization, responsible for providing regulatory expertise, leading complex GCP audits and inspections,

Job Overview: The Sr.Director, Enterprise AI Enablement is responsible for establishing, governing, and scaling Artificial Intelligence capabilities across Fortrea. This role serves as the enterprise leader for AI adoption, AI literacy, Responsible AI governance, and the operational framework suppor

Company Overview: As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and techno

Job Overview: The Senior Director, IT Products, Clinical Pharmacology Services & Laboratories leads technology product management and innovation for Fortrea’s Clinical Pharmacology Services (CPS) business — its clinical research units (clinics) where participants are hosted and dosed, and its bioana

Job Overview: We are looking for a dynamic Product Owner to lead the translation of clinical operations needs and opportunities into innovative digital products and capabilities. The Product Owner will partner with clinical operations stakeholders, end users, Product Management, and technology teams

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

Job Description ****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 healt

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: Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as the Clinical Project Manager (CPM) within the core project team. CTLs partner with the Project Manager and other functional leads to ensure successful delivery of the clinical aspects of a

Clinical Pharmacologist, FSP – Neurology/Immuno Oncology & Metabolic – Remote US Responsibilities Through the application of pharmacological training, expertise and relevant therapeutic area experience , the Clinical Pharmacologist (CP) participates in the following: the development, conduct and rep

Our FSP team is seeking Project Managers to join our growing team. This role requires 2-5+ years of global project management experience, with experience in Neuro/Gen Med, Immuno Oncology or Metabolic. Candidates must be based in the United States. Job Overview: At times working under the direction