Cheruku Vennela

Pharm.D graduate With 10 Months of hands-on experience as a Clinical Research Coordinator Intern, Supporting Phase III trial experience across Cardiology and Pulmonary therapeutic areas. Coordinated end-to-end patient management for 12 study participants, maintained 100% ICH-GCP compliance across 3 concurrent trials, and supported Site Qualification and Site Initiation Visits. Proficient in EDC systems (Medidata, Clario, Calyx), Trial Master File maintenance, IP accountability, and adverse event documentation.

Seeking an opportunity to contribute to Clinical Research, clinical research operations clinical trial management role where I can apply my clinical research knowledge and contribute to high – quality clinical trial execution.

Clinical Research Intern - Gleneagles Aware Hospital - Hyderabad

(2025-09)

• Coordinated 3 concurrent Phase III clinical trials across Cardiology and Pulmonary therapeutic areas, ensuring protocol adherence and data integrity throughout all study phases.
• Managed end-to-end patient coordination for 12 study participants, encompassing screening assessments (inclusion/exclusion criteria), randomization, and scheduled follow-up visits — contributing to 0 screen-failure documentation errors.
• Supported Site Qualification Visit (SQV) by evaluating site feasibility and Site Initiation Visit (SIV) by coordinating protocol training, regulatory documentation, monitoring visits, and audit readiness.
• Maintained Trial Master Files (TMF) per ICH-GCP and regulatory standards; prepared and submitted Ethics Committee documentation on schedule.
• Executed Investigational Product (IP) accountability and reconciliation, including daily temperature log monitoring, ensuring zero cold-chain deviations recorded.
• Identified, documented, and escalated protocol deviations and violations to the Principal Investigator, maintaining full compliance with ICH-GCP guidelines.
• Obtained informed consent documentation under investigator supervision, safeguarding participant rights and regulatory compliance.
• Resolved data queries in EDC systems (Medidata, Clario, Calyx) in a timely manner, maintaining data accuracy and minimizing query backlog.
• Reviewed and maintained Investigator's Brochures (IB), keeping study teams updated on product safety and procedural changes.

Clinical & Hospital Posting - Mamata Academy of Medical Sciences

(2022-01 - 2025-12)

• Audited IP & OP case sheets across multiple departments to verify accuracy of documentation and treatment compliance.
• Participated in pharmacovigilance activities including systematic ADR identification, assessment, and data entry into reporting systems.
• Reviewed patient case sheets for diagnosis, investigations, and prescribed therapy during ward rounds, building clinical decision-making acumen.
• Assisted in medication chart reviews and delivered patient counseling sessions under clinical supervision.

Doctor of Pharmacy - Pharmacy - Chilkur Balaji College of Pharmacy (2026-06)