HARSHA VARDHAN REDDY SINGAM

Detail-oriented Clinical Research Professional with over two years of experience in clinical pharmacy, pharmaceutical sciences, and quality assurance. Proven expertise in supporting clinical trials under GCP and GMP standards, safeguarding participant welfare, coordinating study logistics, managing documentation (CRFs, EDC), and maintaining protocol adherence. Skilled in medical terminology, subject recruitment, and regulatory compliance. Proficient in troubleshooting study-related issues, collaborating with study monitors, and ensuring accurate and timely data entry. Adept in Microsoft Office Suite and committed to maintaining a safe and efficient study environment under the direction of Principal Investigators.

Clinical research professional with over two years of hands-on experience supporting ethically conducted in hospital and GMP-regulated environments. Skilled in participant recruitment, protocol adherence, case report form (CRF) management. Demonstrated ability to collaborate with investigators, monitor regulatory compliance, and maintain data integrity. Contributed to audits and antimicrobial resistance studies, ensuring accuracy in clinical documentation and patient safety. MSc in Pharmaceutical Sciences at the University of Greenwich, enhancing my knowledge of clinical trial regulations and investigational product workflows.

 MSc in Pharmaceutical Sciences with Industrial Practice at the University of Greenwich, UK (2023–2024), with a strong focus on formulation development, regulatory compliance, and clinical research methodologies. Completed a Bachelor of Pharmacy (2015–2019) from Chalapathi Institute of Pharmaceutical Sciences, building foundational expertise in pharmacology, pharmaceutical chemistry, and patient-centered care.