Sr. Research Associate

The role involves supporting method development, method validation, and sample analysis while ensuring full compliance with GLP, GCP, Q1/Q2 guidelines, and all applicable regulatory standards.The Analyst and Senior Analyst will support analytical studies in the clinical research domain, focusing on analytical method development, validation, and sample analysis of E & L / Elemental. The candidates will contribute to the execution of analytical projects in compliance with Q1, Q2 residual analysis, GLP (Good Laboratory Practices), GCP (Good Clinical Practices), and applicable regulatory requirements.Maintain accurate and complete documentation, including lab notebooks, SOPs, protocols, and reports.Process raw data and generate reports for study documentation and regulatory submission.Troubleshoot bioanalytical methods and equipment issues, providing solutions to improve performance.Oversee and implement quality control measures for all bioanalytical processes, including internal audits.

We are looking for skilled Sr Research Associate with 3–5 years of experience in the clinical research domain, specializing in Extractables & Leachable (E&L) and Elemental analytical studies.