SRI VARSHINI CHERUKU
Prosper,TX
Summary
Clinical researcher coordinator with over 2 years of experience working with physicians and medical staff to correlate hospital procedures with clinical trials and reports. Proven experience with regulations regarding research projects. Produced accurate documents, and reports while maintaining a compassionate relationship to study participants.
Versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities.
Experience in working on PHASE II, PHASE III,PHASE IV CARDIORENAL, PSYCHIATRY TRAIL STUDIES.
Overview
5
5
years of professional experience
1
1
Certification
Work History
Primary Clinical Research Coordinator
Dallas Renal Group, Liberty Research Center
05.2025 - Current
- Followed informed consent processes and maintained records.
- Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Experience in Cleaning EDC QUERIES, like veeva Vault, IRave medidata.
- Experience in IRT portal like suvoda, Advara, IQVIA.
- Experienced working in complex study procedures like EKG, Blood pressure measurements.
- Enrolled in the Phlebotomy classes will be a certified phlebotomist by july 2025.
- Have experience in cardio Renal clinical Trial Studies.
- Took a lead on three IgA nephropathy studies and 2 Cardiovascular studies.
- Responsible for preparation and maintenance of regulatory documents for clinical trial Submissions.
- Primary point of contact for the studies with the medical monitors.
- Experience in lab processing's, shipping and packaging of the collected biological samples.
Clinical Researcher Coordinator 1
Revival Research Institute
09.2024 - Current
- Designs clinical trials and plans research protocols
- Ensures that standards of good laboratory practices are met
- Liaises with other medical researchers.
- Coordinated multiple clinical trials, including Phase Ib, II and III studies, in therapeutic areas such as oncology, cardiology, and Nephrology, Psychiatry.
- Oversaw daily trial activities, including subject screening, enrollment, and monitoring for a Phase III oncology trial.
- Collected and managed clinical data for over 150 patients, ensuring compliance with study protocols and regulatory requirements.
- Collaborated with the clinical trial sponsor and research team to prepare regulatory submissions and progress reports.
- Assisted in patient recruitment and retention for a Phase II study investigating the efficacy of a new antihypertensive drug.
- Administered informed consent to study participants, ensuring understanding of risks and procedures.
- Managed the collection of patient data, including laboratory tests and adverse event reporting.
- Acted as a primary point of contact for enrolled subjects, ensuring compliance with study timelines and data accuracy.
- Assisted with the management of investigational drug supplies, including proper storage and distribution.
- Took part in lab processing, storing and packing of biological samples according to study protocols and study specific Lab manuals.
- Have experience in Addressing EDC queries: ¡Mediata, Rave.
- Experience in source build for new studies.
- Took part in Pl oversight, Study-start up and study-close-out.
- Addresses lab queries in labcorp, PPD.
- Performed e-consent in IQVIA.
- Softwares: Realtime CTMS, Clario portal, Suvoda, IWRS, MS outlook, MS EXCEL, EMR.
- Took part in payment for study visits for the Participants.
- Involved in inventory for the site and Placing orders for supplies and kits for study specific protocols.
- Actively participated in Randomization of Subjects.
Clinical Research Intern
Apollo Hospitals
01.2020 - 01.2021
- Company Overview: India
- Assisted in the preparation of study documentation, including case report forms, patient recruitment materials, and informed consent forms for clinical trials in oncology and cardiology.
- Supported the Clinical Research Coordinator and Principal Investigator in day-to-day operations, including participant screening and data collection.
- Monitored patient visits and maintained accurate patient records, ensuring compliance with Good Clinical Practice (GCP) and institutional regulatory guidelines.
- Assisted in data entry and data cleaning tasks using
- Participated in study team meetings, contributing to discussions on protocol amendments and patient safety monitoring.
- Conducted literature reviews to support research and development of new clinical trial protocols.
- India
Education
Doctor OF Pharmacy (PHARM D) -
OSMANIA UNIVERSITY
01.2020
Skills
- Adverse event tracking
- Case report management
- Participant screening
- Informed consent
- Reporting SAE's and AE's
- Maintenance and submission of regulatory Documents
- Lab processing, packing and shipping
- Research experience
- Specimen handling
- Trial management
- Trial oversight
- Phlebotomy
- Dispensing oversight
- Specimen collections
- Meeting coordination
- Schedule coordination
- Participant recruitment
- Test environment establishment
- Data collection techniques
- Report preparation
- Database organization
- Medication dispensing
- Good clinical practices
- Records maintenance
- Data analysis
- Research sops understanding
Certification
- Good Clinical Practice Certifications
- Pharmacy Technician Certification (PTCB)
- HIPAA certification
- IATA CERTIFICATION
- CCRC - Clinical research coordinator certification
- GCP CERTIFICATION
- BLS CERTIFICATION
Research Interests
- Emerging drugs in the fields of cardiology, nephrology, psychiatry oncology and infectious disease
- Gene therapy, particularly for cancer and heritable diseases
- Precision Medicine
Personal Information
Immigration Status: Greencard Holder
Timeline
Primary Clinical Research Coordinator
Dallas Renal Group, Liberty Research Center
05.2025 - Current
Clinical Researcher Coordinator 1
Revival Research Institute
09.2024 - Current
Clinical Research Intern
Apollo Hospitals
01.2020 - 01.2021
Doctor OF Pharmacy (PHARM D) -
OSMANIA UNIVERSITY
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