Sri Gayathri Chebrolu
Glenn Heights,TX
Summary
Dedicated clinical research coordinator experienced in complying with study protocols, standard operating procedures, and good clinical practices. Practiced problem-solver with strong attention to detail. Prepared to offer several years of experience in the field and take on a fast-paced position. Adapt to coordinating all aspects of clinical research studies, from recruitment to data analysis, with a strong focus on patient safety and data integrity. Proven ability to work collaboratively with multidisciplinary teams and effectively communicate complex information.
Overview
2
2
years of professional experience
Work History
Clinical Research Coordinator
Syneos Health
05.2021 - 01.2022
- Coordinating the day-to-day activities of the research study team specifically engaged in carrying out the research clinical protocol
- Preparing research study advertisements submission to the institutional review board (IRB) for approval aid in recruitment
- Performing input, retrieval, and analysis of data for processing and validation, and maintaining research databases on Excel
- Managing calendars and conducting telephone, and face-to-face interviews, or sending emails for follow-up visits as per protocol to administer data collection instruments
- Conduct and document study visits and procedures, including vital signs, medical history, and medication review
- Collaborate with investigators, sponsors, and other team members to ensure the study's success
- Participate in the development of study-related documents, such as protocols, informed consent documents, and case report forms (CRFs)
- Accompanied the clinical research manager while interacting with patients directly
- Coordinated procurement and shipment of necessary equipment and research specimens
- Reviewed clinical data and assisted the clinical research manager in providing reports and presentations
- Initiate submission of regulatory documents to applicable research sub-committees, VA R&D committee, and sponsors
- Maintained accurate records of Adverse Events, expedited reports of Serious Adverse Events, and conducted neurocognitive assessments and mental status exams throughout a patient's treatment
- Collaborated with Pharmacists and Medical Oncologists to build and manage patient treatment plans
Clinical Research Coordinator
Dr. Reddy
08.2019 - 03.2021
- Assisted in the management of clinical trials from start-up through close-out
- Conducted patient screenings and eligibility assessments by study protocols
- Maintained accurate and up-to-date regulatory documents and study binders
- Provided training and support to research staff and study team members
- Facilitated site monitoring visits and resolve any issues identified by monitors
- Utilized Tableau to create visually compelling data reports and dashboards, enhancing management's understanding and facilitating data-driven decisions
- Ensured that the data is handled securely and in compliance with laws such as HIPAA (Health Insurance Portability and Accountability Act)
- Coordinated multiple clinical trials, ensuring adherence to study protocols and regulatory requirements
- Managed patient recruitment, and informed consent processes, and maintained communication with participants throughout the study
- Collaborated with Principal Investigators to develop study protocols and amendments
- Monitored patient progress, recorded adverse events, and reported findings to the Institutional Review Board (IRB)
- Utilized Electronic Data Capture (EDC) systems to ensure accurate and timely data entry and management
- Conducted regular site visits and audits to ensure compliance with Good Clinical Practice (GCP) guidelines
Education
Masters in Health Informatics -
Sacred Heart University
06.2023
Bachelor of Dental Surgery -
Dr NTR University of Health Science
02.2020
Skills
- Clinical Trial Management
- Patient Recruitment and Retention
- Regulatory Compliance (ICH-GCP, FDA)
- Data Collection and Analysis
- Protocol Development
- Adverse Event Reporting
- Electronic Data Capture (EDC) Systems
- Excellent Organizational Skills
- Strong Interpersonal and Communication Skills
- Case report management
- Documentation Management
- Good clinical practice
- Schedule Coordination
- Data Analysis
- Site Management
- Clinical Research Ethics
- Informed Consent Process
- Task Prioritization
Timeline
Clinical Research Coordinator
Syneos Health
05.2021 - 01.2022
Clinical Research Coordinator
Dr. Reddy
08.2019 - 03.2021
Masters in Health Informatics -
Sacred Heart University
Bachelor of Dental Surgery -
Dr NTR University of Health Science
Similar Profiles
Lauren M. Wahl-RiversLauren M. Wahl-Rivers
Clinical Research Associate II at Syneos HealthClinical Research Associate II at Syneos Health
Marshonda WootenMarshonda Wooten
Engagement Center Specialist at Syneos HealthEngagement Center Specialist at Syneos Health
Marie Emmanuelle Koffi KouameMarie Emmanuelle Koffi Kouame
Results Analyst II – Immunology at Syneos HealthResults Analyst II – Immunology at Syneos Health
Tracy ToppTracy Topp
Associate Director, Clinical Trial Management at Syneos HealthAssociate Director, Clinical Trial Management at Syneos Health
Tonia HollowayTonia Holloway
Lead Customer Care Associate at Neiman Marcus DirectLead Customer Care Associate at Neiman Marcus Direct