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 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
• Gather site insights and use CRM tools to track progress and measure impact
• Support clinical trial execution and protocol compliance
• 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
• Participate in global or local task forces and initiatives
• Conduct continuous risk assessment with the Central Monitoring team
• Monitor clinical sites for study-performance and patient-safety issues
• Implement preventative and corrective action plans to mitigate risk and promote compliance
• Identify, evaluate, and recommend investigators and sites
• Ensure timely, accurate data submission and safety-event reporting
• Maintain audit and regulatory inspection readiness
• Manage investigator payments as required by executed contracts

Clinical Research jobs in Michigan

Clinical Research Associate II – Immunology