Research Associate
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About The Position
The Research Associate position at ICON plc in San Antonio, TX, is a part-time role designed for individuals looking to contribute to clinical research in a dynamic and inclusive environment. As a world-leading healthcare intelligence and clinical research organization, ICON is committed to fostering innovation and excellence in clinical development. The Research Associate will work in a PRN (as needed) capacity, coordinating with the Clinical Research Coordinator (CRC) and Study Manager to ensure the execution of all clinical study protocol activities in compliance with Good Clinical Practice (GCP) and Food and Drug Administration (FDA) regulations. This role is crucial in supporting the preparation and execution of clinical studies, ensuring that all activities align with sponsor expectations and ICON Development Solutions. In this role, the Research Associate will be expected to recognize and exemplify ICON's core values, which emphasize a commitment to people, clients, and performance. The position involves familiarizing oneself with and applying all Standard Operating Procedures (SOPs) relevant to the job description. The Research Associate will assist in the early planning phases of clinical studies, including preparing study source document charts, maintaining clinical study enrollment logs, and assisting in filing study documents. Additionally, the role includes participating in initiation meetings, assisting with quality checks on source documents, and ensuring that all required results are filed for subject enrollment verification. The Research Associate will also be involved in various administrative tasks, such as coordinating training with clinical staff, assisting with phone contacts to subjects, and participating in sponsor and monitor visits as required. This position offers an excellent opportunity for individuals looking to gain experience in clinical research while contributing to the success of clinical studies at ICON.
