Harsha K Rajasimha Email and Phone Number
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Harsha K Rajasimha, Ph.D., is a serial entrepreneur, scientist, patient advocate, and philanthropist. Harsha is Founder and CEO of Jeeva Clinical Trials Inc.(https://jeevatrials.com) a AI-driven unified platform for sponsors to execute modern clinical trials with efficiency and universal accessibility. Harsha serves as the founder chairperson of the Indo US Organization for Rare Diseases (https://indousrare.org), where he is forging a new era of cross-border cooperation among various stakeholders of rare diseases in the US, India, and globally by convening the annual Indo US bridging RARE Summit (https://summit.indousrare.org) and the Abbey Meyers Khushi Bridging RARE Awards Gala. Harsha’s 20 years of experience in precision medicine data research spans academia, federally funded research, healthcare and life science consulting, and multiple startups. Harsha made bold career moves after losing a newborn child to a rare congenital disease in 2012 and his younger brother with juvenile diabetes in 2017. He decided to apply his years of postdoctoral training at NIH and FDA to combat rare diseases. At Jeeva, Harsha leads the development of a unified software platform for efficient clinical trials for rare and common conditions that are universally accessible. He knew that technology is not the limiting factor and that patient-centered design guided by stakeholder needs and regulatory requirements would be critical ingredients of the continuously learning digital platform. By digitizing and automating manual repetitive tasks and reducing the logistical burdens on patients and study teams by over 70%, Jeeva accelerates the process of bringing new medicines or vaccines to diverse patients who need them anywhere by over 3x faster.Harsha maintains academic affiliation at George Mason University since 2012 and has authored 17+ publications, book chapters, and patents. Harsha’s work has been recognized by Lead India Foundation 2020 Award for leadership and outstanding achievement in rare diseases, a travel award to join the NGO Committee on Rare Diseases at the United Nations headquarters, New York City in Feb 2019, NTT DATA Healthcare Life Sciences Silver award for outstanding achievement 2017, Sanofi Genzyme patient advocacy leadership award 2016, Bioscience company of the year 2014, NEI director’s innovation award 2012 for building their genomics data infrastructure. Harsha earned his M.S. in Computer Science (2004) and Ph.D. in Genetics, Bioinformatics and Computational Biology (2007) from Virginia Tech.
Jeeva Clinical Trials Inc.
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Founder & CeoJeeva Clinical Trials Inc. Feb 2019 - PresentManassas, Va, UsJeeva is a modern clinical trial control room with one-login, one-subscription solution for efficient clinical trial execution with universal access to patients. Vision, Strategy and Execution of Innovative unified digital health (eClinical) platform Startup focused on addressing the most pressing problems in clinical research: protocol complexity, patient recruitment & retention, patients travel burden, investigator site burden, manual repetitive tasks, and need for 30 different point solutions. Advisory consultant to biopharmaceutical & medical device sponsors, CROs, government grants and contracts, academic medical centers (AMCs), patient foundations, and other health research organizations. Recipient of NSF-ICorps grant 2019 & Montgomery County Bioscience Company of the Year 2014, Prince William County IGNITE Grant 2021, Virginia Governor's commonwealth commercialization fund grant 2021 and 2022, featured in the Everest PEAK Matrix 2021, 2022, and 2023. -
Founder And Executive ChairmanIndousrare Nov 2019 - PresentHerndon, Va, Us"IndoUSrare", an independent non-profit organization focused on helping patients with rare diseases of Indian origin in the USA, India and globally with a vision to build collaborative bridges between the east and the west to accelerate research and development of diagnostics and therapies through education, advocacy, research & grants.Member, Rare global advocacy leadership council, Globalgenes, Platinum member of NORD, Collaborator with numerous organizations in the US, India, and globally.Represent global data and research disparity perspectives at various global rare diseases forums, events, conferences. -
Member Of The Board Of AdvisorsInstitute For Biohealth Innovation Jan 2023 - PresentFairfax, Va, Us -
Clinical Trials Working Group: Rare Disease Diversity CoalitionBlack Women'S Health Imperative Apr 2022 - PresentWashington, District Of Columbia, UsI serve on the Rare Disease Clinical Trials steering committee of the Rare Disease Diversity Coalition (RDDC). -
Member Of The Board Of AdvisorsSynergy Bis Aug 2017 - PresentReston, Virginia, Us -
Member Board Of DirectorsGreater Gift Jan 2022 - Mar 2024Winston-Salem, North Carolina, UsGreater Gift is a 501 (c)(3) non-profit organization whose mission is to help the public understand the powerful role clinical trial volunteers play in the development of new drug therapies, medicines, and vaccines. -
Mindshare Class Of 2022Mindshare, Inc. Jan 2022 - Dec 2022Its an honor and privilege to graduate and become a part of the #Mindshare community of #CEOs #DMV. Access to 1000+ successful #Founders of product companies in the DC, MD, VA region. If you are one (of a product company) and like to join ping me for a referral to this elite community network #Mindshare2022. -
Co-Founder And Co-Chair, Board Of DirectorsOrganization For Rare Diseases India Sep 2012 - Nov 2019Banglore, Karnataka, InAfter a personal family experience with a rare congenital disease, I set out on a journey of global patient advocacy. Starting with volunteering for Rare Genomics Institute in 2012, I cofounded and assembled a dedicated team of 7 social entrepreneurs in founding ORDI in 2014 as the national umbrella organization for rare diseases in India representing the collective voice of all 70+ million patients. (see attached publication).Represented global data and research disparity perspectives at various global rare diseases forums such as IRDiRC, UDNI, Globalgenes, NORD, World Orphan Drugs Congress, Global commission to end diagnostic odyssey for children with a rare disease, and United Nations.While ORDI was still in its infancy in India in 2016, I founded and chaired a humanitarian non-profit 501c3 organization ORDI in the USA to promote Indian rare disease resources and capabilities in the USA. Winning the Sanofi Genzyme's patient advocacy leadership (PAL) award and playing a key role in organizing the 7th annual undiagnosed diseases network international (UDNI) meeting at New Delhi, IN. Administered two grants from Globalgenes towards engaging Indian rare diseases advocates community with Globalgenes summit at San Diego, CA and bringing Indian rare advocates at a needs assessment workshop at New Delhi, IN. An article in preparation will be published soon. Organized Racefor7 in USA. -
Lead Managing Consultant, Life Sciences And Healthcare TechnologiesNtt Data Services Apr 2016 - Aug 2018Plano, Texas, UsI manage the full life cycle of all R&D programs and hold ultimate responsibility for program success and client satisfaction. My focus is on solving big-picture customer challenges through the design of high-impact, scalable Big Data and technology solutions tailored to the biopharmaceutical and medical devices industry’s demands. In addition, I maintain relationships with top biopharma companies and technology partners. By leveraging my strong scientific and leadership backgrounds across healthcare and life science, I work to align technical solutions with my customers’ strategic goals (target division revenues $170M). Received Silver award for showing outstanding achievement, make an impact on one business segment and positively affect the business unit’s fiscal year initiatives. -
Vice President Global Strategy And DevelopmentStrand Life Sciences Nov 2013 - Apr 2016Bangalore, Karnataka, In Reporting to the Chairman and CEO of this Venture backed company, lead the strategic planning and development of NGS CLIA/CAP labs and tests for oncology and inherited diseases. Spearheaded the launch of StrandAdvantage, a 152-gene pan-cancer panel featuring integrated immunohistochemistry (IHC) markers for molecular diagnosis and first-line therapy selection. By combining lab work with bioinformatics analysis and clinical interpretation, StrandAdvantage allows for more precise therapy selection. Lead the customer adoption of StrandNGS software product, StrandOMICS data analysis / interpretation services, partnerships with an innovative SmartLabTM model. Led filing of major scientific/technical patent effort involving 40+ inventors; contributing as one of the inventors. Lead Strategist for diagnostic regulatory affairs in accordance with CMS and FDA’s most current guidance on LDTs. -
Sr. Director - Bioinformatics And Health ItDovel Technologies Mar 2012 - Apr 2013Mclean, Va, Us Served as technical advisor/subject matter expert contractor to US FDA Office of Regulatory Affairs. The $60M+ contract included LIMS implementation for 14 labs nationwide. Held leadership responsibilities as Functional Head of bioinformatics, LIMS, genomics, and Next-Generation Sequencing research programs. Developed cloud-based NGS bioinformatics solution to FDA involving analysis of 20 exome sequencing datasets from Alzheimer’s patient blood samples, key to efforts to discover biomarkers for early diagnosis of Alzheimer’s/dementia. -
Executive Consultant - GenomicsGenome International Corporation Oct 2010 - Dec 2012Madison, Wi, UsProduct Development: Directed a team of genomic scientists and engineers to architect a web-based software "Genome Explorer" for integrative analysis of NGS data for popular applications such as - DNA-seq, RNA-seq, and Methylome-seq. The software integrates selected open source algorithms, tools and databases into an interactive user-friendly framework. Established a Genomic Services Business Unit: Initiated NGS data analysis and custom Bioinformatics projects with a number of clients.For more information: www.genome.com -
Next Generation Sequencing Cyber Infrastructure And Bioinformatics Research - Retinal DiseasesNational Institutes Of Health Mar 2009 - Mar 2012Bethesda, Md, UsReporting to the CIO and Scientific Director of NEI, NIH.• Architect, Design, Procure, Implement and Administer Cyberinfrastructure to support Next Generation Sequencing laboratory including optimized data analysis workflows for NGS applications such as genomics and transcriptomics.• Statistical analysis of next generation sequencing data (mRNA, Exomes, miRNA, ChIP-seq) and microarray data• Work closely with laboratory personnel to elicit data and software requirements on various laboratory reagents and processes (mice colonies, antibodies, primers, plasmids, images) and provide end-to-end technical implementation support.• Provide full IT support (server-side, client-side, scientific programming, databases, and technical) and collaborate with research investigators and postdocs. -
Senior Software Engineer - Health ItSaic / Nci Feb 2008 - Mar 2009Reston, Va, Us• Software design and development for the Enterprise Vocabulary Services (EVS) project in NCI's cancer common infrastructure of cancer informatics (caCORE) and Biomedical Informatics Grid (caBIG) effortso Implemented a mechanism to restrict access to licensed vocabularies in NCI’s EVS to unauthorized users• Design, develop, test, and document a general purpose NCI Thesaurus report writerTechnologies used: UML, Java, JBoss, Spring, Hibernate, Struts, JSF, Oracle, Ant, Apache-AxisTools: MyEclipse IDE, DBVisualizer, Enterprise Architect, LexBIG -
Research Associate - Software EngineerVirginia Tech - Virginia Bioinformatics Institute Jun 2004 - Feb 2008Blacksburg, Va, UsDesign, development, and deployment of Java and XML webservices. Software visualization plugins development in Java for the PathogenPortal project. Mining biological pathway data from pathway genome databases such as Kyoto Encyclopedia of Genes and Genomes and in house biochemical pathways database. Provide visualization support for web and semantic web based standards for pathway data exchange, namely, Systems Biology Markup Language and BioPAX. Memory Performance tuning of existing software plugins using the DevPartner package. Lead a scientific team on pathway data integration, curation, visualization and analysis with the goal of moving from data to knowledge. Project management.Technologies used: Java, Oracle, XML, RDF/OWL, Perl, PHP, DBVisualizer, Taverna, PathwayToolsPlatforms: Windows, Linux -
Software Design Engineer In TestMicrosoft Corporation, Redmond, Wa May 2002 - Aug 2002Redmond, Washington, UsProgramming and test design projects in the COM+ team at Microsoft’s Redmond campus
Harsha K Rajasimha Skills
Harsha K Rajasimha Education Details
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Virginia TechAnd Computational Biology -
Virginia TechComputer Science And Applications With Bioinformatics Option -
Bangalore UniversityComputer Science And Engineering
Frequently Asked Questions about Harsha K Rajasimha
What company does Harsha K Rajasimha work for?
Harsha K Rajasimha works for Jeeva Clinical Trials Inc.
What is Harsha K Rajasimha's role at the current company?
Harsha K Rajasimha's current role is Human-Centric Software and Turnkey CRO Solutions for Modern Clinical Research | #BridgingRare.
What is Harsha K Rajasimha's email address?
Harsha K Rajasimha's email address is ha****@****adx.com
What is Harsha K Rajasimha's direct phone number?
Harsha K Rajasimha's direct phone number is +154023*****
What schools did Harsha K Rajasimha attend?
Harsha K Rajasimha attended Virginia Tech, Virginia Tech, Bangalore University.
What are some of Harsha K Rajasimha's interests?
Harsha K Rajasimha has interest in Children, Drug Discovery, Agrigenomics, Entrepreneurship, Genomic Sequencing Technologies, Bioinformatics, Education, Science And Technology, Clinical Genomics, Alchemy.
What skills is Harsha K Rajasimha known for?
Harsha K Rajasimha has skills like Bioinformatics, Genomics, Life Sciences, Genetics, Perl, Dna Sequencing, Sequencing, Biochemistry, Data Analysis, Lifesciences, Informatics, Databases.
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