Tarek Kazamel

I am a Senior Clinical Research Associate (Independent Consultant) bringing over 14 years of clinical research experience, specializing heavily in high-complexity oncology, CAR-T, and cell/gene therapy (CRT) trials. I deliver high-tier monitoring support to study teams with minimal onboarding friction, and I am immediately available for independent 1099, Corp-to-Corp (C2C), or W2 contract opportunities.

I manage accelerated study timelines and provide rigorous safety reporting for acute toxicities, including CRS and ICANS. I also handle intricate cellular product logistics with strong command of chain-of-custody (COC) and chain-of-identity (COI) requirements—ensuring operational precision in complex trial environments.

Based in Los Angeles, I provide optimized West Coast coverage for Pacific and Mountain time zone sites while staying flexible for nationwide and international travel, including cross-border monitoring in the United States and Canada. With MD, MBA, and PMP credentials, I bring clinical judgment plus executive project management discipline to enforce data integrity, drive site compliance, and maintain audit readiness across FDA and Health Canada frameworks.