Versatile clinical research professional with a strong background in coordinating patient information, laboratory samples, and compliance documents for diverse clinical trials. Highly organized, detail-oriented, and possessing excellent planning and problem-solving abilities. Possesses strong technical and project management skills, is adept at operational frameworks, and is implementing innovative solutions for continuous improvement. Excellent interpersonal and communication skills to establish and maintain effective relationships with internal and external stakeholders. Experienced in cross-functional collaboration, and ensuring regulatory compliance within tight deadlines.