Ranjith Gowda

Clinical programming and data review professional with a B.Pharm, M.Sc. in Bioinformatics, and Advanced Diploma in Clinical SAS. Currently working as a Clinical Data Analyst, reviewing clinical trial data, performing R and SQL checks, identifying discrepancies, and working with data management teams to resolve queries. Hands-on experience with SAS, Python, and R for data validation, cleaning, and analysis, including CDISC SDTM datasets.

Interested in applying these skills to clinical programming, data quality checks, edit checks, and clinical reporting.

Clinical Data Analyst at Janani Bio Solutions (2026-05 – Present)

• Review clinical trial datasets for completeness, accuracy and protocol compliance using SAS and SQL checks.
• Work with clinical and data management teams to raise and resolve queries and discrepancies, keeping data traceable from source to clean dataset.
• Track open data quality issues and support clinical database updates.
• Keep documentation aligned with SOPs and study protocols so records stay audit-ready.
• Learning the full study data flow, including centralized monitoring.

Python and Data Analysis Intern at QSkills (2026-04 – 2026-04)

• Built data validation and cleaning workflows in Python and SQL to find and correct dataset errors, improving accuracy and consistency.
• Prepared analytical reports and summaries in Excel for timely reporting.

Clinical Bioinformatics and Data Analysis Intern at St. John's Research Institute – Cancer Biology (2025-12 – 2025-12)

• Reviewed and processed genomic and clinical research data as part of a cancer genomics research team, coordinating with researchers and bioinformaticians on data specifications.
• Performed NGS quality control, sequence alignment, and variant calling to support integration of clinical and genomic datasets.
• Documented analytical workflows and results in line with research documentation standards, supporting peer review and clear communication of findings.

Industry Training Intern at C-Chem Pharmaceuticals Pvt. Ltd (2023-05 – 2023-05)

• Managed documentation and adhered to rigorous quality-control practices within a regulated pharmaceutical environment.
• Developed a strong foundational understanding of international compliance standards, including ICH guidelines, Good Clinical Practice (GCP), and Good Laboratory Practice (GLP).
• Gained exposure to regulatory affairs frameworks and the end-to-end drug development life cycle.
• Studied the clinical trial process, focusing on procedural compliance, data integrity, and safety protocols.

Master of Science (MSc) in Bioinformatics – Garden City University, Bangalore (2024-09 – 2026-06)

Advanced Diploma in Clinical SAS – Clinilaunch Research Institute, Bangalore (2024-02 – 2024-09)

Bachelor of Pharmacy (B.Pharm) – Mallige College of Pharmacy, Bangalore (2019-05 – 2023-12)