Susanna Thomas

About Susanna Thomas

A detail oriented and quality driven life science professional with 4 years of experience in pharmaceutical and health care industries including 3 years of experience in CRO environments. Proficient in Good Documentation Practices (GDP), GCP, ICH guidelines and regulatory and SOP compliance clinical and analytical documentation. Demonstrated success in quality control reviewing, data verification and document integrity. Passionate about contributing to patient safety and regulatory excellence through data driven insights and documentation accuracy.

Experience

1. Reporting Associate Ii

   Labcorp

   Jul 2022 — Present · Bengaluru, IN

   Experienced in preparing and reviewing clinical documentation with strong focus on data accuracy, regulatory compliance, and submission readiness. Demonstrated ability to compile final clinical and non-clinical study reports by extracting data from LIMS, TRFs, SOPs, and protocols. Skilled in performing comprehensive quality control (QC) of clinical and analytical documents including data tabulation, formatting, and consistency checks in alignment with GCP, ICH, and internal SOPs. Adept at ensuring documentation audit-readiness and supporting regulatory inspections through meticulous QC of raw data, LIMS outputs, and finalized reports. Proven track record in managing multiple studies simultaneously, resolving data inconsistencies, and delivering high-quality outputs under tight deadlines. Strong understanding of Good Documentation Practices (GDP) and, contributing to reporting compliance.

Education

• Amrita School of Biotechnology

  Msc Biotechnology

  2019 — 2021

• Amrita School of Biotechnology

  BSc Biotechnology