Lokesh Pudukarapu
Bloomington,IL
Summary
Accomplished Clinical Research Associate with almost 4 years of experience performing and documenting pre-study site evaluations, regulatory document collection, interim monitoring, and study close-out visits. Diligent in performing studies aligned with good clinical practices, study-specific requirements, and clinical monitoring plans. In-depth knowledge of company procedures, regulatory requirements and quality standards.
Overview
4
4
years of professional experience
2
2
Languages
Work History
Clinical Research Associate
GANDHI INSTITUTE OF MEDICAL SCIENCES
10.2020 - 06.2023
- Conducted clinical trial in accordance with protocol and recorded and monitored progress.
- Coordinated and scheduled protocol-related visits and required testing to demonstrate vigilance in patient safety, protocol compliance and data quality.
- Gathered and organized clinical trial documentation to meet rigorous standards for site approval.
- Reviewed data queries and listings and worked with study centers to resolve data discrepancies.
- Conducted initiation, monitoring and closeout visits to verify study procedures, regulatory documents and data completion.
- Developed strong relationships with investigators and site personnel to ensure ongoing compliance with study requirements.
- Monitored safety of human subjects and oversaw consent procedures to comply with local and federal regulations.
- Maintained site monitoring schedules to facilitate effective communication with members of clinical team.
- Created and maintained database and records filing system to document data on specimen collection, processing and storage.
- Collaborated with cross-functional teams to successfully meet project timelines and deliverables.
- Liaised with clinical investigator to identify, assess and resolve site performance, quality and compliance issues.
- Monitored unit budget to meet financial objectives for spend rate and funding.
- Monitored patient safety throughout clinical trials and reported any adverse events.
- Managed patient recruitment, informed consent process and data entry to support trial objectives.
Clinical Research Coordinator
MALLA REDDY UNIVERSITY - SCHOOL OF ALLIED HEALTH SCIENCES
08.2019 - 09.2020
- Collected data and followed research protocols, operations manuals, and case report form requirements.
- Assessed patients'' eligibility criteria following strict adherence to inclusion/exclusion guidelines.
- Trained new team members on essential clinical research protocols and procedures, promoting a culture of continuous learning.
Education
Master of Science in Information Technology Management (MSTM) -
Lindsey Wilson University
Columbia, Kentucky05.2025
Doctor of Pharmacy - CLINCAL RESEARCH, PHARMACOLOGY
St. Peter's Institute of Pharmaceutical Sciences
WARANGAL, INDIA07.2019
Skills
Strong communication
Interests
Magazines, Medical journals, Research, Laboratory studies, Emerging technologies
Timeline
Clinical Research Associate
GANDHI INSTITUTE OF MEDICAL SCIENCES
10.2020 - 06.2023
Clinical Research Coordinator
MALLA REDDY UNIVERSITY - SCHOOL OF ALLIED HEALTH SCIENCES
08.2019 - 09.2020
Master of Science in Information Technology Management (MSTM) -
Lindsey Wilson University
Doctor of Pharmacy - CLINCAL RESEARCH, PHARMACOLOGY
St. Peter's Institute of Pharmaceutical Sciences