Aditi Sharma

Motivated Clinical Research professional with hands-on experience as an Intern Clinical Research Coordinator, supporting and managing clinical trial activities. Proficient in patient recruitment, screening, and enrollment while ensuring adherence to GCP and regulatory requirements. Experienced in IRB documentation, site coordination, and monitoring activities, with a commitment to advancing clinical research quality and patient safety.

Intern Clinical Research Coordinator - Max Super Speciality Hospital, Patparganj Delhi - Delhi, India

• Executed patient pre-screening, recruitment, follow-up, and data entry in eCRF; resolved EDC queries within defined timelines
• Managed informed consent (ICF) process, safety reporting, and maintained complete source documentation
• Coordinated daily clinical trial activities in collaboration with the Principal Investigator, ensuring protocol adherence and ICH-GCP compliance
• Performed investigational product (IP) management including dispensing, temperature monitoring, accountability, and storage documentation
• Prepared and submitted documents to Ethics Committee (EC); managed EC communications, notifications, and regulatory correspondence
• Maintained Investigator Site File (ISF) and provided regular study status updates
• Ensured with internal teams to complete study trackers, address EDC queries, and ensure timely EC notifications
• Supported site feasibility assessments and qualification visits
• Verified logs and ensured compliance with storage requirements

Master in Clinical Research - Clinical Research - Max Healthcare (2025-01)

Bachelor of Biotechnology - Biotechnology - Mody University of Science and Technology (2021-01 - 2024-12)

12th Up Board (PCB) - Physics, Chemistry, Biology - S. V.

Vidya

Mandir, Ghaziabad, UP (2021-01 - 2021-12)

10th UP Board - Ganga Inter College (2018-01 - 2018-12)