Haripriya Mandayam

Developed patient educational brochures and booklets for disease awareness and treatment guidelines, ensuring medical accuracy by collaborating with physicians and clinical teams to translate complex concepts for the general public.

Maintained SOPs and checklists for biosimilar monoclonal antibody production, coordinated with QA and regulatory teams to ensure GMP compliance, and monitored laboratory instrument calibration and operation.

Authored and reviewed 30+ clinical trial documents including protocols, ICFs, CSRs, and source documents; conducted regulatory submissions to Ethics Committees and registered trials on CTRI while ensuring alignment with approved labeling and guidelines.

Completed a certificate program in biosciences focusing on practical skills for biomanufacturing and regulatory compliance.

Completed an M.Sc. in Biochemistry with coursework and training relevant to clinical research and scientific communication.

Completed a B.Sc. with majors in Chemistry, Botany, and Microbiology providing foundational knowledge for laboratory and research roles.