Our client, a fast-paced Clinical Research Organization (CRO) specializing in oncology, is seeking a dedicated and experienced Clinical Research Associate (CRA) to support critical trials. This role will be based out of

Fort Worth, Texas, US

, but offers a remote work arrangement. The CRA will be responsible for monitoring clinical trial sites to ensure compliance with study protocols, Good Clinical Practice (GCP) guidelines, and all applicable regulatory requirements. This includes conducting site initiation visits, routine monitoring visits (remote and on-site as needed), and close-out visits. You will manage the collection and review of essential study documents, verify data accuracy, and ensure timely resolution of data queries. The CRA will also serve as the primary liaison between the investigative sites and the study team, providing training and support to site personnel. Building and maintaining strong relationships with investigators and site staff is crucial for trial success. The ideal candidate will have a strong understanding of oncology drug development and clinical trial processes. Proficiency in EDC systems, CTMS, and eTMF is required. Excellent organizational skills, attention to detail, and the ability to travel (up to 50% when required for essential on-site visits) are essential. We are looking for individuals with a Bachelor's degree in a healthcare or life science field and a minimum of 3 years of direct CRA experience. Strong verbal and written communication skills are a must. This remote position requires a proactive and self-motivated individual who can manage their time effectively and work autonomously while remaining a valuable part of a collaborative global team. Join us to contribute to life-saving cancer research and make a tangible difference in the lives of patients.