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Aishwarya Loliyekar

@aishwaryaloliyekar

I support high-quality clinical research through accurate data management, documentation, validation, and ICH-GCP-compliant study coordination.

India

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What I'm looking for

I'm looking for an opportunity in clinical data management or clinical research where I can support accurate, ICH-GCP-compliant study data, strengthen my EDC and trial documentation experience, and contribute to high-quality clinical trials.

I've supported clinical research at Healthway Hospitals, maintaining research databases, reviewing source documents, and verifying study data for accuracy, completeness, and protocol compliance.

I handle clinical data collection, entry, validation, cleaning, CRF review, documentation queries, and study-record management. I coordinate with physicians and research teams to support timely data collection and reporting.

During clinical department, bioavailability, and bioequivalence internship work, I contributed to EDC concepts, data reconciliation, documentation, and ICH-GCP-aligned trial workflows.

I've also contributed to pharmacoeconomics and pediatric nephrotic syndrome research, including two peer-reviewed national-journal articles, case reports, systematic reviews, manuscript preparation, and clinical data analysis.

Experience

Work history, roles, and key accomplishments

Research Office Assistant

Healthway Hospitals PVT LTD

Oct 2024 - Apr 2026 (1 year 6 months)

Assisted investigators in clinical research studies involving clinical data collection, review, verification, and documentation. Maintained accurate research databases and supported protocol compliance in accordance with ICH-GCP guidelines.

Clinical Data Management Clinical Data Collection Data Entry Data Verification Data Validation Data quality review CRFs Review Source Data Review (SDR)Query Management ICH GCP Regulatory Documentation Study Coordination Adverse Drug Reaction (ADR) Documentation literature review Excel Tracking and Reporting Research Register Maintenance Clinical Trials Data Management

Intern in Clinical Department and BE and BA

KLE College of Pharmacy

Nov 2023 - Jan 2024 (2 months)

Assisted in Bioavailability (BA) and Bioequivalence (BE) clinical studies, supporting clinical data collection, entry, verification, and documentation. Participated in Case Report Form (CRF) review and study documentation activities.