Prasanna Kumar Kodali
Sunnyvale,CA
Summary
- Highly skilled pharmaceutical research professional with extensive experience in in-vivo and in-vitro studies, particularly in oncology research
- Proficient in conducting mammalian cell culture in a BSL-2 environment, cell-based assays, and utilizing animal models for in vivo studies
- In vivo work includes tumor inoculation and measurement, various dosing methods (Oral, SC, RO, IP, IV), and blood/tissue collection for model development
- In vitro work includes cancer cell-based assay design, assay development and drug testing
- Adept in various laboratory techniques including Flow cytometry, FACS, ELISA, and fluorescence microscopy for cell and tissue analysis
- Extensive laboratory skills adhering to Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) standards
- Experienced in designing and executing cell culture media experiments, maintaining precise records, aseptic technique
- Skilled in chemical characterization assays, evaluating immune responses, RNA extraction and analytical testing
- Strong skills in biology, statistical analysis, and technical writing
- Expert in cell-based assays (flow cytometry, proliferation, cytotoxicity, cytokine release) with a background in immune cell biology
- Good understanding of immune cell functional assays, multi-color flow cytometry, primary cell isolation/culture
- Proficient in RNA/DNA isolation, qPCR, cloning, and virus production
- Experienced in histology, immunohistochemistry, assay development, and laboratory compliance
- Strong ability to design experiments, solve scientific problems, and maintain lab protocols and equipment
- Strong IT skills including project management, data analysis, and proficiency in MySQL with familiarity in Python programming
- Skilled in research methodology, literature reviews, and biostatistics for robust scientific investigations
- Skillful in utilizing Microsoft Office applications such as Excel, PowerPoint, and Word
- Thorough understanding of FDA, EMA, ICH, and GCP guidelines
- Knowledgeable about advanced drug delivery systems, drug development, and clinical trials
- Extensive understanding of pharmaceutical research, molecular biology, microbiology, Immunology, cell biology
- Extensive experience in molecular biology
- Proven track record in western blotting, PCR, DNA sequencing
- Proficient in executing experiments, monitoring cell culture quality, and supporting technology transfer and manufacturing activities
- Passionate about innovation and dedicated to maintaining a strong research-oriented mindset
- Committed to continuous learning, enhancing skills, and improving the technical knowledge base
Overview
7
7
years of professional experience
Work History
Research Scientist Intern
Johnson & Johnson
New Brunswick
02.2024 - 06.2024
- Spearheaded the design and execution of pioneering in vivo studies, including patient-derived xenograft (PDX) models and humanized mouse models, to accurately recapitulate human cancer conditions and drive translational research efforts
- Applied project management expertise to support critical activities, including timeline creation, risk assessment, and mitigation plan development, ensuring efficient and effective execution of research projects
- Actively participated in ideation sessions and think tanks, contributing insights and perspectives that catalyzed the development of novel cancer therapies, diagnostic tools, and personalized treatment approaches.
Senior Research Associate
Syngene Biocon Limited
10.2020 - 06.2022
- Designed and executed xenograft experiments to evaluate the efficacy of novel anti-cancer compounds in vivo
- Established patient-derived xenograft (PDX) models to mimic human cancer conditions, contributing to translational research
- Managed xenograft colonies, including implantation, monitoring tumor growth, necropsy procedures and imaging analyses.
Product Quality Analyst
Dr. Reddy's Laboratories
Hyderabad
05.2017 - 06.2018
- Assisted the Quality Assurance (QA) team in conducting quality audits and inspections to ensure adherence to current Good Manufacturing Practices (cGMP) across multiple manufacturing facilities
- Supported the preparation process for regulatory inspections by organizing relevant documentation and facilitating inspection activities
- Gained hands-on experience in a GMP-compliant manufacturing environment, fostering a deep understanding of quality assurance processes.
Education
Masters in Technology Management Science -
Lindsey Wilson College
01.2024
M.S in Pharmacology and Regulatory Toxicology -
NIPER- (National Institutes of Pharmaceutical Education and Research)
01.2020
Bachelor of Pharmacy -
Sri Venkateshwara college of Pharmacy
01.2017
Skills
- Research Expertise
- Oncology research
- Mammalian cell culture
- Cell-based assays
- Animal models
- Fluorescence microscopy
- Cancer biology
- PKPD studies
- Imaging studies
- Bioinformatics
- Research methodology
- Literature reviews
- Data analysis
- Biostatistics
- Pharmaceutical Knowledge
- Molecular biology
- Microbiology
- Advanced drug delivery
- Clinical trials
- Project management
- Risk management
- Problem-solving
- MySQL
- Python programming language
- GLP standards
- GMP standards
- Strong research-oriented mindset
- Analytical thinking abilities
- Excellent communication skills
- Collaboration skills
- Attention to detail
- Meticulousness
- Adaptability
- Eagerness to learn new techniques and technologies
- Experimental design
- Research methods
References
References available upon request.
Timeline
Research Scientist Intern
Johnson & Johnson
02.2024 - 06.2024
Senior Research Associate
Syngene Biocon Limited
10.2020 - 06.2022
Product Quality Analyst
Dr. Reddy's Laboratories
05.2017 - 06.2018
Masters in Technology Management Science -
Lindsey Wilson College
M.S in Pharmacology and Regulatory Toxicology -
NIPER- (National Institutes of Pharmaceutical Education and Research)
Bachelor of Pharmacy -
Sri Venkateshwara college of Pharmacy
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