Your Trusted Partner in Clinical Research
Working with me means more than just expertise — it's about a personal, hands-on approach that larger firms can't always provide. No layers, no handoffs — just reliable, dedicated support from someone who's fully invested in your clinical research goals.
Hi, I'm Adi Davidi, a Good Clinical Practice (GCP) expert with over 20 years of experience as a dedicated Lead Clinical Research Associate (CRA), Project Manager, Clinical Program Manager (CPM), and lecturer in the healthcare sector.
I hold a BSc in Biotechnology from the Technion – Israel Institute of Technology, where I graduated in 2002. I began my career at Pharma Clinical, an Israeli Contract Research Organization (CRO), where I worked from 2003 to 2011. During that time, I gained extensive insights into clinical research, regulatory compliance, and trial management.
For over a decade, I have been delivering GCP lectures and courses to various forums, including students, medical teams, and research coordinators. I provide these sessions both in-person and online, sharing my expertise with audiences around the world.
In July 2022, I made the exciting move from Israel to Austin, Texas, where I continue to pursue my passion for clinical research. I am fluent in both Hebrew and English, which enables me to communicate effectively with diverse teams and stakeholders across the globe.
GCP training tailored to various audiences: foundational courses for students, in-depth training for medical teams, and targeted courses for research coordinators. Delivered in-person or online.
Professional auditing services including site audits, process audits, and regulatory audits. Detailed audit reports with actionable recommendations and follow-ups.
Specialized services in Standard Operating Procedures for clinical trials. SOP review to ensure alignment with GCP standards, and SOP drafting tailored to your specific needs.
Tailored ethical consultancy including risk assessment, regulatory alignment with FDA, EMA, and GCP standards, informed consent support, and participant rights protection.
Comprehensive support for clinical trials across all phases: site selection and setup, trial monitoring and oversight, data management and reporting, subject recruitment and consent.
Adi has been an invaluable member of my team in various roles. I have closely observed her strong work ethic, growth, and remarkable contributions. Adi is a highly dedicated and talented professional who consistently demonstrates a commitment to excellence. Her technical skills, attention to detail, interpersonal abilities, leadership, problem-solving, and creativity have made a significant positive impact on the team. Always approachable and willing to help, she is a true asset to any organization.
Adi brings unparalleled professionalism to everything she does, but what truly sets her apart is her warm and approachable nature. Working with her is always a delight.
Have questions or need support? Whether you're looking for guidance, expert advice, or just someone to help you navigate the process, I'm here to assist. Let's work together to ensure you achieve your goals with confidence and ease.