Chaithra Kumar Email & Phone Number

India

• Develop and draft comprehensive trial protocols, outlining the purpose, methodology, and objectives of the study.• Present trial protocols to steering committees, ensuring clear communication of research goals and methodology.• Design and create case report forms (CRFs) for accurate data collection, ensuring adherence to regulatory standards.• Coordinate with ethics committees to ensure compliance with regulations safeguarding the rights and safety of trial subjects.• Manage regulatory authority applications and approvals, overseeing the process for research and marketing authorization of pharmaceuticals, while adhering to industry regulations and guidelines.

Bengaluru, Karnataka, India

During my time at ICBio, I participated in a rigorous program featuring six-month internships per semester at respected CROs/SMOs and pharmaceutical firms. Through these immersive experiences, I gained valuable expertise in protocol design, document preparation, medical writing, project management, regulatory submissions, and proficient data handling. This comprehensive journey refined my practical skills and positioned me as a competent professional within the industry.

Bangalore Urban, Karnataka, India

• Conducted insect sample sorting and accurately identified insects according to their orders, specializing in bee identification and specimen pinning.• Assisted in gathering research subject information from records and aided in specimen collection, ensuring meticulous attention to detail.• Demonstrated proficiency in conducting research projects using standardized techniques and protocols, contributing to the advancement of scientific knowledge.• Executed entry-level research tasks in support of ongoing projects, maintaining precision and adherence to established procedures.• Provided essential support to research staff by performing basic data entry functions, ensuring the accuracy and integrity of research data.