Clinical Research

• Advance AbbVie's clinical research pipeline by striving for excellence in clinical research
• Partner with investigators and site staff to support meaningful and effective clinical-trial engagements
• 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, protocols, and patient-treatment principles
• Conduct site evaluation, site training, routine monitoring, and site-closure monitoring
• Ensure compliance with protocols, monitoring plans, applicable regulations, GCPs, ICH Guidelines, SOPs, and quality standards
• Develop and customize site-engagement strategies for assigned studies
• Gather local and site insights and use CRM tools to report, track, and measure strategy impact
• Evaluate and ensure effective patient 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 provide development input
• Participate in global or 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, evaluate, and recommend investigators and clinical sites
• 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

Clinical Research jobs in Connecticut

Clinical Research Associate II – Oncology