Riya Sachan

Hi, I’m Riya Sachan, a biotechnology professional with a master’s degree in Pharm. Biotechnology from NIPER-Raebareli. I have a strong interest in clinical research, regulatory documentation, and drug safety, and I’m eager to apply my knowledge in pharmacovigilance and scientific writing.

I’ve worked with PCR, Real-Time PCR, DLS-Zeta Sizer, and spectrophotometric techniques, and I’m well-versed in Good Clinical Practice (GCP) and Good Manufacturing Practices (GMP). I enjoy working with data management, compliance, and research-based roles, and I’m always looking to expand my skills in the evolving field of life sciences and healthcare

I have a strong academic background in M.S. (Pharm.) Biotechnology from NIPER-Raebareli, with a keen interest in clinical research, regulatory documentation, and drug safety. My experience includes working with pharmacovigilance processes, scientific writing, and data management, ensuring compliance with Good Clinical Practice (GCP) and Good Manufacturing Practices (GMP). I have hands-on expertise in molecular biology techniques such as PCR, Real-Time PCR, DLS-Zeta Sizer, and spectrophotometry, which have strengthened my analytical and technical skills.

I am detail-oriented, highly organized, and passionate about contributing to clinical trials, safety data analysis, and research-driven roles in the pharmaceutical and healthcare industry.

I am pursuing my M.S. (Pharm.) in Biotechnology from NIPER-Raebareli, where I gained in-depth knowledge of biopharmaceutical research, clinical research methodologies, and regulatory compliance. My academic training has provided me with a strong foundation in drug safety, pharmacovigilance, and scientific documentation, along with hands-on experience in molecular biology techniques such as PCR, Real-Time PCR, DLS-Zeta Sizer, and spectrophotometry. Additionally, I have a B.

Pharmacy degree, which has further strengthened my understanding of pharmaceutical sciences, quality assurance, and Good Clinical Practices (GCP). This educational background has equipped me with the necessary skills to contribute effectively to clinical research, regulatory affairs, and drug development.