Clinical Research

• Advance AbbVie’s clinical research pipeline and support innovative medicines and solutions
• Serve as the primary point of contact for investigative sites
• Provide clinical-trial context 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, site training, routine monitoring, and site closure activities
• Ensure compliance with protocols, monitoring plans, regulations, GCPs, ICH Guidelines, AbbVie SOPs, and quality standards
• Develop and customize site-engagement strategies for assigned studies
• Gather local and site insights and use CRM tools to track progress and measure impact
• Support clinical-trial execution by applying protocol, scientific, and clinical-trial knowledge
• Evaluate recruitment and retention techniques based on the patient disease journey
• Develop therapeutic-area, asset, clinical-landscape, and patient-journey knowledge
• Mentor and train less experienced CRAs and contribute to their development
• Participate in global or local task forces and initiatives
• Conduct continuous risk assessment with the Central Monitoring team to identify study-performance and patient-safety issues
• Resolve site risk signals and implement preventative and corrective action plans
• Identify, evaluate, and recommend investigators and sites for planned clinical studies
• Ensure quality and timely submission of site data, including safety-event reporting and follow-up
• Maintain audit and regulatory inspection readiness at assigned sites
• Manage investigator payments according to executed contract obligations, as applicable

Explore Clinical Research Associate II at AbbVie. Review requirements and application details.