About the job
Join AbbVie in advancing our clinical research efforts, transforming scientific breakthroughs into life-changing treatments for patients. As a pivotal member of our team, you will collaborate closely with investigators and site staff, ensuring AbbVie is the premier choice for clinical trials. Your focus on site clinical research will enhance data integrity, compliance, and overall study performance, contributing to an exceptional customer experience.
Key Responsibilities:
- Serve as the primary liaison for investigative sites, possessing a high level of expertise in clinical trial information and strengthening AbbVie’s reputation.
- Align, train, and motivate site staff and principal investigators regarding clinical trial objectives, protocols, and patient treatment principles, fostering trust and collaboration.
- Conduct site evaluations, training, and routine monitoring while adhering to regulatory standards, Good Clinical Practices (GCP), ICH Guidelines, and AbbVie’s Standard Operating Procedures (SOP).
- Utilize an advanced understanding of site engagement to customize strategies for assigned studies, incorporating local insights and CRM tools to track progress and measure effectiveness.
- Demonstrate a deep understanding of the study protocol and clinical trial execution, ensuring effective recruitment and retention based on patient journeys.
- Mentor and train less experienced Clinical Research Associates (CRAs), contributing to their professional development and participating in global/local initiatives as directed by management.
- Engage in continuous risk assessment, collaborating with the Central Monitoring team to proactively monitor site activities for potential study performance or patient safety issues.
- Utilize critical thinking skills to address site risks and implement preventative and corrective action plans to enhance compliance and ensure a patient-centric approach.