Clinical Research Associate II - Oncology MN

Role: Clinical Site Monitor focused on site engagement and trial execution within AbbVie's oncology and immunology pipelines. Objectives include ensuring protocol compliance, data integrity, patient safety, and fostering strong investigator relationships. Responsibilities encompass site evaluation, training, ongoing monitoring, risk assessment, and supporting patient recruitment strategies. The role also involves mentoring less experienced CRAs, overseeing data quality, and ensuring audit readiness. Qualifications: Tertiary health qualification preferred; minimum 1 year of clinical research monitoring experience, including risk-based monitoring; knowledge of ICH/GCP guidelines and local regulations; strong collaboration, planning, organizational, and interpersonal skills. High-Value: Oncology and immunology therapeutic areas, clinical trial monitoring, risk-based approaches, investigator site management, data quality assurance, regulatory compliance, and trial phase (implied to be Phase 1-3). WorkSetup: Not specified, but implies field-based monitoring with site interactions.