Clinical Research

• Advance AbbVie's clinical research pipeline and turn science into medicine for patients
• Serve as the primary point of contact for investigative sites
• Provide contextual information on clinical trials and connect stakeholders with investigative sites
• Align, train and motivate site staff and principal investigators on trial goals, protocol 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, SOPs and quality standards
• Develop and customize site engagement strategies for assigned studies
• Gather site insights and use CRM tools to track progress and measure impact
• Connect study protocols, scientific principles and clinical trial requirements to day-to-day execution
• Evaluate recruitment and retention techniques based on the patient disease journey
• Develop therapeutic-area, asset, clinical-landscape and patient-journey knowledge to support recruitment and protocol compliance
• Mentor and train less experienced CRAs and contribute to their development
• Participate in global/local task forces and initiatives
• Conduct continuous risk assessment with the Central Monitoring team to identify study performance or patient safety issues
• Resolve site risk signals and implement preventative and corrective action plans
• Identify and evaluate potential investigators and sites
• Ensure quality and timely submission of site data, 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.

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