
Versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples, recruitment strategies and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities, dedicated to supporting team objectives and can be relied upon to contribute effectively.
Proficiency in various research methodologies, data collection and management using EDC systems
Familiarity with clinical assessment tools, pharmacology principles, laboratory techniques, statistical analysis software, and EHR systems
Adherence to study protocols and regulatory standards, knowledge of GCP guidelines, and patient recruitment strategies
Demonstrates adept communication, sharp critical thinking, and seamless collaboration with interdisciplinary teams
IATA
IATA
ICH-GCP