Clinical Research Associate II

Role: Clinical Site Liaison responsible for site engagement, monitoring, and ensuring trial quality in AbbVie's clinical research. Objectives include building trusted site relationships, facilitating effective trial conduct, and supporting patient recruitment and retention in immunology, oncology, or neuroscience studies. Responsibilities encompass site evaluation, training, risk management, data quality oversight, and regulatory compliance, with an emphasis on risk-based monitoring and site performance improvement. The role involves mentoring less experienced CRAs, collaborating with cross-functional teams, and ensuring audit readiness. Qualifications: tertiary health-related degree preferred; minimum 1 year of clinical research experience, including 6 months in monitoring investigational trials; knowledge of GCP/ICH guidelines and regulatory requirements; strong interpersonal, organizational, and technological skills. Preferred: familiarity with specific therapeutic areas, risk-based monitoring approaches, and advanced site engagement tools. The position requires excellent communication skills, integrity, and the ability to operate effectively in a fast-paced environment. Work setup details or travel expectations are not specified.