• Building comprehensive Bio-scientific information management services, software and databases using BioC and other industry standard tools
  • Clinical, Bio-statistics and Bioinformatics consulting by group of scientists armed with BioC and other bioinformatics tools
  • Technical support for building Bioinformatics infrastructure
  • Technical support in software development using our libraries of routines for scientific data analysis and manipulations
  • Our capabilities include: Services in Clinical data analysis, Bio-statistics, Bioinformatics, Protein Structure Modeling, Microarray and other large-scale data analysis
 
  • Scientific Software Developer
    • Ph.D. (Physics and Mathematics)
    • Expertise in Software Development, Bioinformatics, Nanotechnology, Quantum Physics, Chemistry, Molecular Simulations and Artificial Intelligence.
    • Developed multiple know-how algorithms for information analysis, manipulation and prediction
    • Recent significant contributions: development of protein family hierarchy analysis and annotation toolbox, biological activities of organic molecules and bioassays information resource, Bio- and Medical-Informatics exploration and discovery toolbox, genome assembly and annotation engine, simulation software for protein and DNA interaction with nano-media
    • Author of +40 publications in Physics, Chemistry, Biology
    • Professional experience in most of the modern IT hardware and software technologies


  • Bioinformatics Scientist
    • Ph.D. (Biology)
    • Expertise in developing procedures and software for analysis and visualization of high-throughput biological data
    • Significantly contributed to internationally renowned molecular biology information resources and software tools related to complex DNA and protein sequence analysis, protein classification, molecular evolution, comparative genomics, proteomics data analysis
    • 7+ years of industry, non-profit and academic experience


  • Computational Biologist
    • Ph.D. (Biology)
    • Expertise in molecular modeling, DNA and protein sequence analysis, protein classification, microarray data analysis and gene network and pathway analysis
    • Track record of algorithm development using ANNs and HMMs.
    • Experienced in developing workflows and analysis pipelines for automation
    • 10+ years of industrial and academic work experience


  • Structural Bioinformatics Specialist
    • Ph.D. (Biology)
    • Structural Biologist by training, solved several structures by X-ray crystallography
    • Additional skills include structure based modeling, RNA biology and bioinformatics
    • Experience in working on renowned molecular information resources
    • Contributed significantly to the development of novel tools for doing structure analysis and modeling
    • Unique expertise of combining sequence and structure information
    • 9+ years of work experience.


  • Computer Scientist
    • Ph.D. (Chemistry)
    • Expertise in programming, Bioinformatics and ChemInformatics
    • Member of OMG (Object Management Group: http://www.omg.org/) and co-author of CORBA (http://www.corba.org/) standard in ChemInformatics.
    • Skill set: platforms - UNIX clones, Win32, .NET, Win16, DOS, MacOS, Netware, OS/2, Java, QNX, Windows CE, Palm OS, Symbian OS; computer Languages - C/C++, C#, Java, SQL, PL/SQL, Delphi, Pascal, Perl, VB, FORTRAN, Assembler x86/386+; web- HTML/DHTML, XML/XSL, JavaScript, VBScript, ASP, ASP.NET, PHP, JSP, WML, VRML; technologies - MFC, OWL, COM/DCOM, CORBA, OLE, J2EE, *.NET; CASE - Rational Rose, RUP, ErWin, BpWin, Visio 98 2003, UML; DBMS - Oracle, SQL Server, DB2, FoxPro, Informix, Interbase, Sybase, MySQL, PostgreSQL, Paradox. Member of OMG (Object Management Group: http://www.omg.org/) and co-author of CORBA (http://www.corba.org/) standard in ChemInformatics. Technical support in software development using our libraries of routines for scientific data analysis and manipulations


  • Biostatistician
    • M.S. (Statistics)
    • Expertise in statistical and programming activity for large projects, SAS programming with the proven experience in developing statistical programs, performing analysis and data validation for epidemiological studies and microarray data.
    • 7+ years of industry and academic experience.


  • Clinical Trial Auditor
    • B.S. (Biology)
    • Expertise in Domestic and International Clinical Research Trial Audits- established expertise in Good Clinical Practices (GCP) auditing to comply with FDA regulations, International Congress on Harmonization (ICH) Guidelines, specific company SOPs/guidelines and local governmental regulations
    • Expertise in Pre-study site evaluation and setup; Ongoing data verification, test article accountability, and study file monitoring; Study-site closeout visits; In-house prospective and retrospective clinical study data collection and CRF completion; Query management
    • Expertise in audits of Final Study Reports/NDA submissions/Safety Reports/IND updates
    • 12+ years of experience.


  • Medical Writer
    • M.S. (Microbiology)
    • Expertise in development of FDA IND Safety Updates, development of NDA/PLA submissions/updates, design and implementation of clinical project workflow/timelines.
    • 12+ years of experience.