Job Description: Advance AbbVie’s clinical research pipeline and support the development of innovative medicines Serve as the primary point of contact for investigative sites Provide clinical trial information and connect stakeholders with investigative sites Align, train, and motivate site staff and principal investigators on trial goals, protocols, and patient treatment principles Conduct site evaluation, training, routine monitoring, and site closure activities under supervision Ensure compliance with protocols, monitoring plans, regulations, GCPs, ICH Guidelines, AbbVie SOPs, and quality standards Customize site engagement strategies and track progress using CRM tools Connect study protocols, scientific principles, and clinical trial requirements to day-to-day execution Evaluate and support patient recruitment and retention plans Develop therapeutic-area, asset, clinical-landscape, and patient-journey knowledge Conduct continuous risk assessments with the Central Monitoring team Resolve site risk signals and implement preventative and corrective action plans Identify, evaluate, and recommend investigators and clinical sites under supervision Ensure data quality and timely submission, including safety-event reporting and follow-up Maintain audit and regulatory inspection readiness Manage investigator payments according to executed contracts, as applicable Requirements: Appropriate tertiary qualification in health-related disciplines (Medical, Scientific, Nursing) preferred, or experience or equivalent work experience Clinically related experience, preferably in clinical research coordinating or data management Knowledge of appropriate therapeutic area indications preferred Ability to understand and apply scientific concepts to clinical trial conduct Knowledge of local regulatory and legal requirements, ICH/GCP Guidelines, and applicable policies Ability to work collaboratively and cross-functionally Planning and organizational skills; ability to work effectively in a dynamic environment with competing projects and deadlines Ability to leverage technology, tools, and resources Critical thinking and good judgment to address clinical site issues Strong written, verbal, active listening, and presentation skills Ability to establish and leverage site relationships and trusted partnerships Integrity in accordance with AbbVie code of business conduct and leadership values Self-motivated and focused on timely, quality outcomes in a fast-paced environment Benefits: Paid time off (vacation, holidays, sick) Medical, dental, and vision insurance 401(k) Short-term incentive program eligibility Equal opportunity employment Reasonable accommodations for applicants with disabilities