Ankita Salunkhe – Transforming Clinical Research: The Future Awaits

CV of Ankita Salunkhe

Personal Summary

A motivated Clinical Research Coordinator with hands-on experience in coordinating and managing clinical trials. Skilled in patient recruitment, informed consent, data collection, and maintaining regulatory compliance. Seeking to contribute to impactful clinical research while continuing to build a strong foundation in clinical operations and GCP standards.

Academic Qualification

• MSc – Shivaji University – 2023 – 83%
• BSc – Shivaji University – 2021 – 9.1/10

Skillset and Professional Learning

• NIDA Clinical Trials Network certificate- Good Clinical Practice
• Global Health Training Centre: INTRODUCTION TO CLINICAL RESEARCH
• Professional Diploma in Clinical Research, Clinical Data Management, and Pharmacovigilance

Experience

1. Clinical Research Coordinator (Dec 2024 – Present)

[Lifepoint Multispeciality Hospital] — [Pune, Maharashtra]

• Coordinated 4 clinical trials – COPD, Asthma, Type II DM, Obesity
• Assisted in screening, enrolling, and following up with patients as per protocol.
• Maintained accurate and timely documentation of source data and CRFs.
• Supported site monitoring visits and audit preparations.
• Managed study supplies, lab samples, and regulatory binders.
• Collaborated with investigators, sponsors, and CROs to ensure protocol compliance.

2. Trainee Clinical Research Coordinator (3 months internship)

[Lifepoint Multispeciality Hospital] — [Pune, Maharashtra]

• Clinical trial coordination
• Informed consent process
• Patient recruitment and retention
• Source documentation & CRF completion
• ICH-GCP guidelines
• IRB/EC submissions
• Protocol adherence
• Safety reporting (e.g., AE/SAE documentation)

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Cover Letter:

A motivated Clinical Research Coordinator with hands-on experience in coordinating and managing clinical trials. Skilled in patient recruitment, informed consent, data collection, and maintaining regulatory compliance. Seeking to contribute to impactful clinical research while continuing to build a strong foundation in clinical operations and GCP standards.