Ruchika Kandunuri

WORK HISTORY

EDUCATION

ABOUT RUCHIKA KANDUNURI

As a dedicated pharmaceutical industry professional, I am committed to contributing to the success of my team through unwavering diligence, meticulous attention to detail, and exceptional organizational skills. With a comprehensive understanding of various aspects of clinical trials. My experience encompasses a wide range of clinical trial functions, including site selection, proactive sponsor liaison, adept handling of regulatory submissions, proficient site initiation, strategic patient recruitment and enrolment strategies, diligent patient follow-up, effective patient retention initiatives, and proficient adverse event (AE)/serious adverse event (SAE) recording and reporting. I am also skilled in source data collection, electronic case report form (eCRF) management, Investigator Site Files (ISF) maintenance, and electronic Trial Master File (eTMF) administration. Experienced Pharmacist in handling prescriptions and advising patients about the disease and medications. Currently, I\'m pursuing a master\'s degree in Regulatory Affairs, driven by a passion to further enhance my expertise in regulatory compliance within the pharmaceutical industry. I am actively seeking opportunities to apply my combined clinical and regulatory knowledge, contribute to innovative projects, and drive positive outcomes in the ever-evolving pharmaceutical landscape.