Shivanandini Thummala
CLINICAL RESEARCH COORDINATOR
NEW HAVEN,CT
Summary
Experienced clinical research professional with a strong background in coordinating patient information, laboratory samples, and compliance documents for various clinical trials. Demonstrates exceptional organizational skills, attention to detail, effective planning, and problem-solving abilities. Skilled in recognizing clinical values and abstract data from source documents, utilizing analytical skills to identify data and patient safety issues.
Overview
5
5
years of professional experience
2025
2025
years of post-secondary education
2
2
Certifications
Work History
Clinical Data Analyst
Fair Haven Pharmacy
, CT
12.2024 - Current
- Analyzing and interpreting clinical and prescription data to identify trends and support patient care strategies
- Ensuring data integrity and assisting in the development of data-driven reports
- Supporting compliance and documentation in alignment with industry regulations
- Enhanced data accuracy by implementing rigorous validation processes and quality control measures.
- Established strong relationships with internal stakeholders such as statisticians, project managers, and clinicians for seamless collaboration on projects.
- Developed custom algorithms for complex data analysis, leading to actionable insights and better decision-making in clinical trials management.
- Conducted periodic audits of database systems, ensuring compliance with regulatory requirements and adherence to industry best practices.
- Maintained thorough documentation of analytical methods employed throughout each project lifecycle, ensuring reproducibility of results when needed.
Clinical Research Coordinator
Nizam's Institute Of Medical Sciences
01.2021 - 07.2023
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- Coordinated and monitored clinical trial activities to support timely and accurate completion of studies.
- Managed patient recruitment, informed consent process and data entry to support trial objectives.
- Prepared detailed informed consent documents to clearly communicate risks, benefits, expectations, rights and responsibilities related to participation in clinical trials.
- Assessed patients'' eligibility criteria following strict adherence to inclusion/exclusion guidelines.
Clinical Informatics Intern
Nizams Institute of Medical Sciences
05.2020 - 12.2020
- Managed and analyzed healthcare data to establish trends and improve patient care delivery.
- Utilized SQL and Excel to develop reports for healthcare professionals to make informed decisions.
- Assisted in the creation of workflows to improve clinical documentation in EHR systems.
- Trained healthcare personnel on best practices for EHR data entry and retrieval to ensure data accuracy and compliance.
- Collaborated with interprofessional teams to improve patient access by streamlining scheduling and referral coordination.
- Supported staff members in their daily tasks, reducing workload burden and allowing for increased focus on higher-priority assignments.
- Gained valuable experience working within a specific industry, applying learned concepts directly into relevant work situations.
Education
Master of Science - Healthcare Informatics
Sacred Heart University, College of Health Professions
Fairfield, CT12-2024
Bachelor of Nursing - undefined
Nizam’s Institute of Medical Sciences
Skills
SQL
Python
R
Tableau
MS Excel
Power BI
MySQL
Microsoft SQL Server
Jupyter Notebook
NumPy
Pandas
Electronic Health Records (One Glance)
Agile methodology
undefinedCertification
Good Clinical Practice (GCP)
Timeline
Clinical Data Analyst
Fair Haven Pharmacy
12.2024 - Current
Clinical Research Coordinator
Nizam's Institute Of Medical Sciences
01.2021 - 07.2023
Clinical Informatics Intern
Nizams Institute of Medical Sciences
05.2020 - 12.2020
Bachelor of Nursing - undefined
Nizam’s Institute of Medical Sciences
Master of Science - Healthcare Informatics
Sacred Heart University, College of Health Professions
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