Suryoday Rathod

Pharm.D graduate with hands-on internship experience in a Phase III clinical trial, supporting core Clinical Data Management (CDM) activities including case report form (CRF/eCRF) review, source data verification, and discrepancy resolution under ICH-GCP and SOP-driven protocols. Well-versed in data integrity principles (ALCOA), adverse event and serious adverse event (AE/SAE) documentation, and Trial Master File (TMF) standards. Known for strong attention to detail, analytical thinking, and clear cross-functional communication.

Seeking to apply these clinical research and data management fundamentals in an entry-level Clinical Data Management Associate role at a CRO or pharmaceutical company.

Clinical Research Intern (CRC), Phase III Clinical Trial at Dr. D. Y. Patil Medical College, Hospital and Research Centre (2025-10 – 2025-11)

• Supported Phase III clinical trial conduct under ICH-GCP guidelines and site SOPs, contributing to protocol-compliant data collection.
• Reviewed source documents against case report forms (CRF/eCRF) to verify completeness, consistency, and accuracy, supporting data cleaning and quality control (QC).
• Cross-checked trial documentation to support discrepancy identification and query resolution, applying ALCOA data integrity principles throughout.
• Assisted with subject screening and the informed consent (ICF) process in line with protocol-defined visit schedules.
• Maintained essential study records, including AE/SAE safety documentation, in accordance with Trial Master File (TMF) and Investigator Site File (ISF) requirements.
• Upheld participant confidentiality and regulatory compliance standards throughout study conduct.

Clinical Pharmacist Intern (CP) at Lokmanya Hospital, Pune and Ruby Hall Clinic, Pune (2025-06 – 2026-06)

• Performed medication therapy review (MTR) and prescription review, verifying data accuracy across patient records.
• Conducted medication reconciliation and drug-drug interaction assessment, cross-referencing clinical data for consistency.
• Monitored and documented adverse drug reactions (ADRs) using structured, protocol-based recording practices, and reviewed case documentation for completeness.
• Interpreted laboratory data for therapeutic monitoring, applying analytical review to clinical datasets.
• Collaborated with multidisciplinary care teams during ward rounds and case presentations, coordinating across roles in a manner consistent with cross-functional stakeholder collaboration in clinical research.

Doctor of Pharmacy in Pharmacy – Dr. D. Y. Patil College of Pharmacy (2020 – 2026)

HSC – Omkar Vidyalaya (2018 – 2018)

SSC – J.V.J. Vidyalaya (2016 – 2016)