Shejal Gundla

Pharmacy-trained clinical research professional with an Advanced Diploma in Clinical Research and nearly 2 years of hands-on laboratory and pharmaceutical manufacturing experience. Equipped with solid knowledge of ICH-GCP guidelines, pharmacovigilance, clinical data management, electronic data capture (EDC), and Good Clinical Practice (GCP). Seeking an entry-level role as CRC, CDM, CRA, CTA, or PV Associate to leverage scientific expertise and clinical research training in a CRO/pharma environment.

Trainee R&D Chemist - YMC India Pvt. Ltd. - Hyderabad

(2023-10 - 2024-12)

• Performed synthesis of Active Pharmaceutical Ingredients (APIs) and impurities under GMP-aligned laboratory conditions.
• Executed flash column chromatography for purification and isolation of chemical compounds.
• Maintained accurate laboratory records, batch documentation, and analytical reports in compliance with regulatory standards.
• Collaborated with R&D and QC teams to evaluate compound purity and yield against specifications.

Junior Research Associate – Process Chemistry - Morepen Proprietary Drug Research Pvt. Ltd. - Hyderabad

(2025-06 - 2025-12)

• Executed large-scale pharmaceutical manufacturing reactions with strict adherence to SOPs and quality compliance protocols.
• Monitored reactions in real time and performed process optimization to improve yield and batch consistency.
• Coordinated with QA, QC, Production, and R&D departments to ensure seamless batch execution and timely documentation.
• Prepared and reviewed batch records, deviation logs, and change control documentation per regulatory requirements.

M.Sc. - Pharmaceutical Chemistry - D.B.F. Dayanand College of Arts & Science, Solapur (2023-03)

B.Sc. - Chemistry - D.B.F. Dayanand College of Arts & Science, Solapur (2021-03)

Advanced Diploma - Clinical Research - Bangalore Clinical Research Institute (BCRI) (2024-01 - 2024-05)