Priya Vella Jr, BSc (Hons) Life Sciences

I am a Clinical Research Coordinator with experience in coordinating clinical trials across academic and healthcare settings. My expertise includes study coordination, participant recruitment, informed consent, regulatory documentation, ethics committee submissions, clinical data management, and ensuring compliance with ICH-GCP guidelines. I have collaborated with investigators, sponsors, and multidisciplinary healthcare teams to facilitate the successful execution of clinical studies while maintaining the highest standards of participant safety, data integrity, and regulatory compliance.

Alongside my clinical research experience, I have been actively involved in medical writing, research methodology, protocol development, systematic reviews, and scientific publications. I am passionate about advancing evidence-based medicine through high-quality clinical research and continuously expanding my knowledge in clinical trial management, regulatory affairs, and emerging technologies, including artificial intelligence in healthcare. My goal is to contribute to innovative research that improves patient care and translates scientific discoveries into meaningful clinical outcomes.