Ruchika Kandunuri
MS Regulatory Affairs I Actively seeking for Jobs in | Regulatory Affairs I Med-devices | Clinical Research.
- Role
- Validation Intern at Piramal Pharma Ltd
- Location
- Boston, MA, US
- LinkedIn followers
- 500 followers
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.
Experience
Validation Intern
Jun 2025 — Present · PA, US
Education
Sri Chaitanya College of Education
Intermediate
2012 — 2014
Malla Reddy Institute Of Pharmaceutical Sciences
Doctor of Pharmacy - PharmD
2013 — 2020
Northeastern University
Regulatory Affairs
2023 — 2025
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