SAUMYA

PharmD graduate with GCP certification and hands-on clinical research/pharmacovigilance training at an NABH-accredited tertiary care hospital. Skilled in developing and managing critical trial documents (ICFs, SIS, regulatory submissions) while ensuring compliance with ICH-GCP and institutional standards. Proven ability to collaborate effectively with cross-functional teams to uphold ethical conduct, reduce protocol risks, and prioritize patient safety. Detail-oriented professional committed to rigorous clinical research.

• Multitasking - As the sole intern managing both the Integrated Liver Care and Oncology/SICU departments for a year, I learned to juggle competing priorities in a fast-paced clinical environment—ensuring high-quality care even under pressure.
• Documentation- Independently handled ADR reporting, dose adjustments, and medication reconciliation, always aligning with clinical protocols and regulatory requirements to maintain accuracy and patient safety.
• Research- Co-authored two clinical case reports during my internship, sharpening my skills in data analysis, medical literature review, and evidence-based writing.
• Accountability- Given critical clinical duties beyond typical intern responsibilities, I proved my reliability, attention to detail, and commitment to patient care and precise documentation.