SAS ,TRAININGS AND PROJECTS @DNA RESEARCH CENTRE

DNA Research Centre and Axis group announces new batches for different Modules in Bioinformatics, Biotechnology, Molecular Biology, and Recombinant DNA Technology. DRC proudly announces its involvement in DNA Forensics and Biotechnology Research. We have updated all the projects available with us and providing more challenging, live and industrial projects with different module of training programmes. DRC are privileged members of ABLE, BCIL, FQS, USP Brazil, Bode Tech Lorton, U.S.A etc and dealing with the companies like Beta Genetics and Face key for a wide range of services.
DRC has been contacted by A.P govt. for a fingerprinting and data mining cum data basing project for stopping fraud of Ration cards and work is in progress. DRC has developed different range of Bioinformatics and Biotechnology projects, some of them include EST data basing for Fruit fly, Human genome project (Cell markers data basing) etc .
BASIC MODULE(30 Days)
CORE MODULE (45 days)
ELECTIVE MODULE (60 days)
ADVANCE MODULE (90 days)
FOUNDATION MODULE (180 days)
IMMUNOINFORMATICS
METABOLOMICS
PATTERN RECOGNITION IN BIOLOGY
PHARMACOINFORMATICS
MEDICAL AND CLINICAL INFORMATICS
CHEMIOINFORMATICS/CHEMICAL INFORMATICS
SAS Clinical Trials/Proteomics/ Genomics etc
WET LABS @ DNA RESEARCH CENTRE
Microbial Biotechnology
Recombinat DNA Technology
Enzymology
Immunotechnology
Plant Tissue Culture
culture media:
Industrial Microbiology
Clinical Microbiology
Microbial Biotechnology

All the listed trainings except the wetlab Practicals are available via Online Mode via our web based facilities.
*Courses for one week and 20days are available, for details email or call us.
Note: Registration open till June 2008 batches.

Administrative office:

DNA Research Centre
12-13-1249, 1st floor
Besdies Andhra Bank
Tarnaka -500017
Hyderabad (India)

LAB Address:

DNA Research Centre
12-8-259/1
Near Aaiyappa Temple
Mettuguda Hyderabad-500017
dnaresearchcentre@gmail.com
www.dnares.in
Phone: +91-40-40180502/9247438983

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For careers @ Clinical research company

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For more details please visit www.clinireach.in
CLINiREACH Clinical services Offers a Distance education program in clinical research with live video classes
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There is a huge gap between demand of trained clinical research professionals and supply. CLINiREACH Clinical Services is a division of CLINiREACH SERVICES (P) Ltd. is a Contract Research Organization decided to fill this gap by training students in this domain. CLINIREACH Clinical Services (Training and Consultancy Division) offers a comprehensive course on Clinical Research, Database Management and Statistical Analysis (SAS®) for students & professionals seeking a career in the multi billion dollar Clinical Research industry
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Opening for Clinical Consultant

We feel that your skills are inline with our current requirements for Sr. Clinical Solution Consultant positions.

Roles and Responsibilities:

· Guide the customer during the initial requirements process so that the EDC specification takes advantage of clients EDC platform capabilities in achieving the functionality needed by the customer.

Work with customer and Application Development team to transfer a clear
understanding of the requirements (including CRF design, edit checks, clinical
workflow), anticipate customer needs (to reduce the likelihood of future change
requests) and remove ambiguity in the requirements process.

Complete and baseline the specification documents (UI wireframes, edit check
and workflow specifications, etc).

Work with the customer to define the data transfer plan, data integration points
and reporting/listing requirements.

Help to define and enforce data collection and data management standards and comply with all regulatory requirements.

Mandatory Skills:

4+ years Experience with clinical trials and the associated clinical operations workflow in bio-pharma and /or medical devices.

Solid understanding of clinical trial protocols, CRF layout, clinical data collection and management issues.Effective communication skills, both oral and written and the ability to engage the customer during the requirements phase and manage customer expectations.

Competent in the use of MS Office, Self directed and detail-oriented.

Ability to collaborate with internal and external teams and work effectively using web-meetings to review and revise requirements.

Knowledge of quality assurance processes in a FDA regulated software development environment.

In case you are interested please send me a copy of your Updated CV to Preejith.shashi@proteans.com or for more information call me Preejith @ 080-66186513

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