Job Description The Clinical Research Associate I (CRA I) is a responsible for supporting the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory guidelines, protocols, and quality standards. The CRA I assists in site selection, initiation, and monitoring visits, reviews study documentation and data for accuracy and completeness, liaises with site staff to address study-related issues, ensures the safety and well-being of study participants, maintains essential study files and assists in the preparation and submission of study documents. The role requires strong organisational skills, attention to detail, effective communication, and a foundational understanding of Good Clinical Practice (GCP) and relevant regulations. It is expected for this role to have up to 80% travel inter-state or overseas as required. This is a unique, entry level opportunity to work with AbbVie, recognised on the Fortune 100 Best Companies to Work For list for the 8th year in a row in 2025! KEY DUTIES AND RESPONSIBILITIES Act as the primary point of contact for the investigative site, providing contextual information on the clinical trials, connecting stakeholder to the investigative sites and strengthening AbbVie’s positioning. Align, train and motivate the site staff and principal investigator under supervision on the goals of the clinical trial program, protocol, and patient treatment principles for the trial ensuring a trusted partnership. Conduct site evaluation, site training, routine, and site closure monitoring activities under supervision, in compliance to the protocol and monitoring plans and accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and to quality standards in conducting clinical research, ensuring safety and protection of study subjects. Customise site engagement strategy for assigned studies under supervision and gather local/site insights and utilise site engagement tools such as the Customer Relationship Management (CRM) tool, to report/track progress and measure impact of that strategy. Fundamental level of competency connecting the study protocol, scientific principles and clinical trial requirements to the day-to-day clinical trial execution activities. Evaluate and ensure effective recruitment and retention techniques/plans based on the patient disease journey. Develop solid knowledge of therapeutic area, asset and clinical landscape / patient journey to enable successful patient recruitment and overall protocol compliance. Responsible for continuous risk-assessment proactively, and in collaboration with Central Monitoring team, monitor activities conducted by clinical sites to detect early overall study performance or patient safety issues. Ability to think critically to resolve site risk signals while having robust understanding of site processes to drive study execution. Ensure preventative and corrective action plans are put into place, as needed, to mitigate risk and promote compliance using a customer centric approach. Identify, evaluate and recommend new/potential investigators/sites under supervision and support from more experienced CRAs. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Ensures audit and regulatory inspection readiness at assigned clinical site at all times. Manages investigator payments as per executed contract obligations, as applicable. Report any adverse event within 24 hours as per AbbVie’s policies and procedures. Proactively participate in AbbVie’s WHS programs, adhere to policies and promote a safe work environment at all times. Adhere to AbbVie’s internal codes of conduct and compliance processes. Other ad hoc duties such as administrative duties, as requested.