Sanket Bobade

Doctor of Pharmacy (Pharm.D) graduate with hands-on experience in clinical research, pharmaceutical R&D support, drug safety, and pharmacovigilance. Proficient in study design, biostatistics (SPSS, GraphPad Prism), ICH-GCP compliance, and scientific writing. Demonstrated track record of conducting observational clinical studies, supporting regulatory submissions, and publishing peer-reviewed research.

Seeking to leverage clinical expertise and research skills in a pharmaceutical R&D or clinical research role.

Clinical Pharmacist Intern – Pharmacovigilance & Clinical Research at District Civil Hospital (2026-01 – Present)

• Conducted clinical safety data validation and signal detection across 100+ patient cases, ensuring full pharmacovigilance compliance and accurate medication therapy outcome documentation.
• Managed drug interaction registries and filed 80+ adverse drug reaction (ADR) reports in accordance with Good Documentation Practice (GDP) guidelines and regulatory standards.
• Led an observational clinical research study on antiretroviral therapy (ART) efficacy in HIV patients, adhering to ICH-GCP principles, study protocol, and ethical compliance.
• Performed quantitative data analysis using IBM SPSS Statistics and GraphPad Prism; applied biostatistical methods for clinical outcomes interpretation and research reporting.
• Collaborated with a multidisciplinary team of 10+ physicians and clinical pharmacologists to optimize patient therapeutic outcomes and medical strategy.
• Conducted systematic literature surveillance across 30+ peer-reviewed journals to support evidence generation, medical advisory protocols, and scientific communication.

Clinical Pharmacology Intern – Antimicrobial Stewardship & Drug Safety at KIMS Kingsway Hospital (2025-06 – 2026-01)

• Participated in 50+ daily prospective audit and feedback rounds across ICU (SICU, MICU, TRICU, HDU, Oncology) to optimize antimicrobial therapy aligned with drug safety and pharmacovigilance principles.
• Evaluated 100+ antibiotic prescriptions weekly for appropriate selection, dosing, and de-escalation strategies based on evidence-based medicine.
• Executed evidence-based therapeutic evaluations and supported medical affairs functions for clinical trial protocols in compliance with global ICH-GCP and WHO standards.
• Co-authored clinical trial safety compliance materials and standard operating procedures (SOPs), ensuring data integrity across intensive care settings.
• Monitored ADRs for active pharmacovigilance and antimicrobial stewardship programs; translated clinical data into actionable medical insights to support product lifecycle management.
• Tracked real-world evidence (RWE) outcomes in immunocompromised oncology patients to inform evidence-based therapeutic decision-making.

Clinical Pharmacist Intern – Regulatory & Safety Documentation at District Civil Hospital (2024-08 – 2025-02)

• Drafted Risk Management Plans (RMP) and post-market surveillance protocols for 3 drug products in alignment with ICH E2E guidelines.
• Supported clinical study reports and patient safety summaries for regulatory submissions, contributing to cross-functional evidence generation.
• Applied research methodology including study design, protocol adherence, data validation, and documentation of study findings.

Doctor of Pharmacy in Pharmacy – K.T. Patil College of Pharmacy – Babasaheb Ambedkar Marathwada University (2020 – 2026)