SAHITHI KANTAMANENI
Houston,USA
Summary
Dynamic research professional specializing in overseeing clinical studies and navigating complex project management. Proven success in ensuring compliance with research protocols while effectively managing multifaceted projects. Recognized for fostering collaborative team environments and adapting to evolving project demands, with a strong track record in data management and regulatory adherence. Committed to driving results and enhancing research outcomes through strategic planning and execution.
Overview
5
5
years of professional experience
1
1
Certification
Work History
Clinical Research Coordinator
Biopharma Informatic
Houston, TX
03.2025 - Current
- Coordinated clinical trial activities to ensure compliance with regulatory standards and protocols.
- Assessed patients'' eligibility criteria following strict adherence to inclusion/exclusion guidelines.
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- Followed informed consent processes and maintained records.
- Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
- Coordinated and monitored clinical trial activities to support timely and accurate completion of studies.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Facilitated clear communication between principal investigators, sponsors, and study participants for seamless trial execution.
Clinical Research Assistant
Biopharma informatics
Houston, TX
09.2024 - 03.2025
- Screened, selected, and enrolled clinical study subjects by reviewing medical records and conducting screening interviews, meeting enrollment goals.
- Obtained informed consent, conduct patient assessments, and collect vital signs and medical histories in accordance with study protocol.
- Monitored participants throughout the trial to ensure their safety, compliance with recommendations, and accurate reporting of adverse events and deviations.
- Developed and handled clinical trial documentation, including case report forms, informed consent forms, and regulatory submissions.
- Handled data queries and followed participants in study activities to comply with study requirements.
Research Assistant
Baylor College of Medicine- Children's Nutrition and Research Center
Houston, TX
01.2024 - 05.2024
- We engaged with participants during house visits to gather data that was compliant with the predetermined protocol.
- We conducted questionnaires or surveys to gather information from study participants.
- I conducted phone interviews to determine each participant's eligibility.
- We developed a video intervention to educate parents about recommended practices and alternatives for screen time.
- Worked with a research team to create, test, and distribute survey instruments for an intervention evaluating the effects of screen use on children's health, particularly regarding sleep and weight.
- We developed a codebook with appropriate responses from the interviews.
Clinical Research Assistant
Alluri Sitharama Raju Academy of Medical Sciences
Vijayawada, Andhra Pradesh, India
04.2021 - 06.2022
- Achieved seamless coordination of clinical trial operations, maintaining strict adherence to protocols and regulatory guidelines.
- Developed effective methods for patient recruitment while ensuring proper screening procedures and obtaining informed consent.
- Captured and managed clinical data with precision while maintaining compliance with source documents and case report forms.
- Maintained participant safety and regulatory compliance by meticulously monitoring, recording, and reporting adverse events.
- Facilitated communication between stakeholders and clinical staff regarding research protocols.
Education
Master's - Public Health: Epidemiology
University of Texas Health Science Center at Houston
Houston, TX05-2024
Bachelor - Medicine and Surgery (MBBS)
NTR university of health sciences
Andhra Pradesh06-2020
Skills
- Documentation management
- Informed consent
- Adverse event reporting
- Study protocols
- Investigational product management
- Good clinical practice
- Time Management
- Attention to Detail
- Microsoft Office
- Work Prioritization
- Critical thinking
- Qualitative and Quantitative Research
- Data Collection
- Teamwork and Collaboration
- Multitasking and Organization
- Interpersonal Communication
- Electronic data capture
- Clinical trial management
Certification
- Social and Behavioral Research
- Biomedical Research
- Responsible conduct of Research
- IATA Certification
- Health Information and Privacy Security (HIPS)
- Good Clinical Practice (GCP)
- Research Conflict of Interest
Languages
Telugu Native
Hindi Fluent
English Fluent
Timeline
Clinical Research Coordinator
Biopharma Informatic
03.2025 - Current
Clinical Research Assistant
Biopharma informatics
09.2024 - 03.2025
Research Assistant
Baylor College of Medicine- Children's Nutrition and Research Center
01.2024 - 05.2024
Clinical Research Assistant
Alluri Sitharama Raju Academy of Medical Sciences
04.2021 - 06.2022
Bachelor - Medicine and Surgery (MBBS)
NTR university of health sciences
Master's - Public Health: Epidemiology
University of Texas Health Science Center at Houston