www.mokshabio.com Moksha Biosciences Hyderabad : Clinical Research/CDM/CLINICAL SAS Training

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    www.mokshabio.com Moksha Biosciences Hyderabad : Clinical Research/CDM/CLINICAL SAS Training

    Moksha Biosciences is a Hyderabad Based Contract Research Organization to Support Global and Indian Pharmaceutical and Biotech companies in their Preclinical, Bio analytical and Clinical Development programs. Our training Division, Moksha Institute of Fundamental Research (MIFR), is offering Corporate training for industrial people and job oriented training for academic students in clinical research.

    Many companies are involved in clinical research and data management services in India and abroad

    Quintiles-Bangalore, Siro Clinpharm- Mumbai, ICON Clinical Research-Chennai, Pharmanet”s(SFBC international)-Bangalore, Asian Clinical Trails-Hyderabad, Clininvent-Mumbai, Dno Clinical Research-Mumbai , Ecron Acunova-Mumbai, Synchron-Banglore, Covance Clinical Research-Mumbai, Parexel-Hyderabad,Prainternational-Mumbai,,Lambda Cinical research-Mumbai and many more………


    There are more than 2,50,000 positions vacant globally and the salaries vary approximately $40000 per annum for clinical research coordinator to almost $100000 per annum for business development manager.

    Course modules
    CLINICAL RESEARCH –Duration 30 days
    1) Introduction to Clinical Research.
    2) Introduction to Drug Discovery and Development
    3) Regulations in clinical research
    4) Designing of clinical research
    5) Essentials for Clinical Monitoring
    6) Bio Ethics in Clinical Research
    7) Roles and Responsibilities of study team.
    8)Introduction to CDISC
    9) Clinical Trial Process.
    10) ICH-GCP
    11) 21 CFR 11
    12) Clinical Data Management Process.

    CLINICAL DATA MANAGEMENT
    ----- Duration 30 days
    1) Protocols and CRF Design
    2) Data management Plan
    3) Good Clinical Practice & Other Regulatory Guidelines
    4) Data Capture Methods and Data Entry
    5) External Data Loading And Data Validation
    6) Statistical Analysis & Reporting
    7) Regulations & Guidelines for CDM
    8) Pharmacovigilance.
    9) EDC (Electronic Data Capture.)
    10) MedDRA
    11) Management of ADR.
    12) OpenClinica.
    13) Oracle Clinical (overview)
    14) Safety Data Management.

    SAS With Clinical Trails
    -----Duration 30 days
    1) Basics of statistics for Clinical
    2) Reporting Clinical Trial analysis.
    3). Introduction to SAS in CDM.
    4) Base/SAS.
    5) SAS/STAT.
    6) SAS/GRAPH.
    7) SAS Macros.
    8) Statistical significance
    9) Custom Derived SAS data sets
    10) SAS-Programming for NDAs (New Drug Applications)
    11) Data Cleaning,

    For more details and registrations send mail to

    cdm@mokshabio.com
    mokshabio@yahoo.com

    ADDRESS:
    1st Floor, opp. Geetha Hospital
    Maruthi Nagar Road
    CHAITANYAPURI, Dilshuknagar,
    Hyderabad-60 ,PH. 9959861177
    Website: http://www.mokshabio.com

    M.PHARM/B.PHARM FINAL YEAR PROJECTS AT MOKSHABIO, HYD.

    Moksha Biosciences is a Hyderabad Based Contract Research Organization to Support Global and Indian Pharmaceutical and Biotech companies in their Preclinical, Bio analytical and Clinical Development programs. Our training Division, Moksha Institute of Fundamental Research (MIFR), is offering corporate training for industrial people in pharmaceutical development programs.

    We are offering job relevant Academic projects for M.pharm/B.pharm final year students


    M.PHAMACY PROJECTS

    M.Pharmacy- pharmaceutics
    M.phaemacy-Pharmacology
    M.pharmacy- pharma.Analysis
    M.pharmacy-pharm.chemistry or Medicinal chem

    B.PHARMACY PROJECTS.

    B.pharmacy-pharmaceticts
    B.pharmacy-Pharma analysis
    B.pharmacy-Regulatory affairs
    B.pharmacy- QC/QA

    We also offer job relevant academic projects in Bioinformatics, Biotechnology, and Drug Designing


    1) New Drug Discovery and design projects in following diseases

    a) Tuberculosis b) Malaria c) Aids d) Diabetics-II e) Parkinson’s f) Brest and Brain Cancer g) Alzheimer’s disease h) Eye disorders I) Hypertensive disorders j) Inflammation k) Cardio vascular disorders.

    2) Bioinformatics projects
    3) QSAR and Docking projects
    4) Molecular Modeling and CADD projects
    5) SAS with Clinical trials projects
    6) Pharmacoinformatics projects
    7) Biomarkers and protein modeling projects


    TRAINING PROGRAMS

    Courses
    1) CLINICAL RESEARCH
    2) CLINICAL DATA MANAGEMENT
    3) SAS WITH CLINICAL TRAILS
    4) PHARMACO VIGILANCE
    5) MEDICAL CODING

    CONTACT

    1)DILSHUKNAGAR

    MOKSHA BIOSOLUTIONS
    3RD FLOOR, PRASHANTH COMPLEX
    OPP: VENKATADRI THEATRE
    DILSHUKNAGAR
    HYDERABAD-38
    mokshabio@yahoo.com
    info@mokshabio.com
    Ph: 995861177


    2) RTC ‘X’ ROADS

    Mokshabiosolutions
    304,sri data sai complex
    Opp: saptagiri theatre
    RTC X OADS
    Hyderabad-26
    mokshabio@yahoo.com
    info@mokshabio.com
    Ph: 9959861177
    www.Mokshabio.com

  2. Post Count Number #2
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    Reply

    HELLO,
    Can you give me your full information about this training

  3. Post Count Number #3
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    Re: Moksha Biosciences Hyderabad : Clinical Research/CDM/CLINICAL SAS Training

    hello sir iam lavanya iam searching for smart openings

  4. Post Count Number #4
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    Raji_SAS_fresher

    Rajyalakshmi Pulla
    E-mail : rajyal10 AT gmail.com
    Objective
    Seeking an opportunity in the field of Clinical Research domain, I am looking forward to an opportunity where I can utilize my experience and skills in contribution effectively to the success of the organization and also further improve my professional and personal skills.
    Professional Summary
    - 4 years of experience in Medical Transcription/Proofreader.
    - PR Accumedscript, Hyderabad, 2009 to 2010
    - MT-PR Medisigma, Hyderabad, 2006 to 2009
    Job Responsibilities :
    - Proofread the jobs done by the MTs and OJTs.
    - Analyze the quality of the job and accuracy of the transcriptionist.
    - Grade the errors and review the errors with the transcriptionist.
    - Counsel the MTs on the ways to improve the quality and quantity.
    - Performing final QA of medical documents for US hospitals and clinics.
    Skill Set :
    - Well versed with anatomy, physiology, drugs, and medical terminology.
    - Good listening and comprehension skills.
    - Well accustomed to structuring, formatting, editing and proofreading medical content.
    SAS COURSE DETAILS
    Name of the institution : Visva Technology, Hyderabad
    Duration of the course : 3 months
    Brief Discussion Of Base SAS Project
    Adverse event is a situation in which the patients are incoherent and respond negatively to the therapeutic drug. By identifying the appearance of most common adverse event/events, client can search/apply for better drug combination in the healing process. Hence identification of AEF (Adverse Event Frequency) is an important task with which the hospital/research lab/pharmaceutical companies are able to identify the suitability of drug or combination of drugs to the individual physical condition upon application.
    Salient Features Of AE Frequency
    1. Data was searched for both missing values and duplicate values. The duplicate values were deleted where as the missing values data was sent back to the client to get the missing information.
    2. With the graphical representation of the adverse event frequency, one can identify the occurrence of AE.
    3. The tabular report also mentioned for AE frequency.
    4. Frequency of AE for each drug can be identified.
    Responsibilities
    1. Designing, building and testing in a series of SAS programs for generation of different data sets.
    2. Developing macros for automatic running of frequency report for each composition.
    3. Accessing data from Excel database and SAS data sets/importing the initial data set from the source file.
    4. Developing reports using PROC REPORT, PROC TABULATE, PROC FREQ and PROC MEANS.
    5. Generating graphs, Gcharts for adverse events for each composition.
    Scholastics
    - M.Sc. (Microbiology), Acharya Nagarjuna University, Guntur, AP, June, 2011 (Expecting results in September)
    - B.Sc (Life Science-Botany, Zoology, Chemistry), Andhra University, Visakhapatnam , 81%
    - Intermediate (Bi. P.C), St. Ann's College for Women, Visakhapatnam, 83%
    - I.C.S.E., St. Ann's Convent School, Visakhapatnam , 72%
    Technical Skills
    - Statistical Packages : SAS.
    - SAS Tools : SAS/BASE, SAS/MACROS, SAS/STAT, PROC/SQL, SAS/GRAPH.
    - Operating System : Windows XP.
    - Office Tools : Ms-word, Excel, Access, PowerPoint.
    - Post Graduate Course in Computer Applications from CMC Ltd, Hyderabad.

  5. Post Count Number #5
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    CURRICULUM VITAE
    G.SRIKANTH email :srikanth.gundawar AT gmail.com
    Career Objective :
    Looking a position that offers me an opportunity for advancement in my career endeavors, where I can utilize my current technical skills, knowledge & can complete my project from conception to completion under a boss who can take best out of me & gives me a chance for my innovative work as well.
    Academic profile :
    Course Institute Name University Year of Passing Percentage
    B.Pharmacy
    (final year) Sitha Institute of Pharmaceutical Sciences Jawaharlal Nehru Technological University 2008-2011 67.3%
    Diploma in Pharmacy
    Gokaraju Rangaraju College Of Pharmacy State Board of Technical Education & Training 2006-2008 78.6%
    Intermediate
    Sri Vijaya Sai Junior College Board of Intermediate Education 1999-2001 76.4%
    SSE Jawahar Navodaya Vidyalaya Central Board of Secondary Education 1994-1999 55%
    Laboratory skills :
    - Have practical knowledge in operating Analytical Techniques U.V Spectrophotometer, Chromatography, Operating of Water’s HPLC with EMPOWER , Dissolution apparatus ,Testing of Disintegration of tablets, Gas chromatography, Friability.
    COMPUTER SKILLS :
    - Operating Systems : MS OFFICE & XP
    - Programming Languages : C
    Project Details :
    "FORMULATION AND EVALUATION OF MOUTH DISSLOVING TABLETS OF DOMPERIDONE BY USING SUPERDISINTEGRANTS"
    - Ease of administration to patient who refuses to swallow tablets such as
    pediatric, geriatric and psychiatric patients.
    - No need of water to swallow the dosage form, which is highly convenient feature for patients who are traveling and do not have immediate access to water.
    - Rapid dissolution and absorption of drug, which will produce quickonset of action

    Presentations :
    - “ FORMULATION AND INVITRO EVALUATION OF OMEPRAZOLE LIPID MICROSPHERE” At APTICON 2010
    - Presented a poster on “Chromotherapy –the healing power of colors” in a national level competition held at Pulla Reddy Institute of pharmacy
    Publications :
    - Formulation and Evaluation of Salbutamol sulphate Fast Dissolving Tablet
    In International Journal of Research in Pharmaceutical and Biomedical Sciences.
    STRENGTHS :
    - Effective communication skills and can express my opinion very clearly in all types of situations.
    - Have a proactive approach to problem solving with the ability to work well in a team.
    - Enthusiastic, detail oriented, independent, interpersonal with strong determination and will power to achieve my goals and good time management skills.
    Conferences Attended :
    - Attended 62nd Indian Pharmaceutical Congress held at Manipal University, Manipal during 17-19 December 2010.
    Extra Curricular Activities :
    - I have been the sports and anti-ragging representative in college.
    - Participated in blood donation camp in College.
    - Participated and distributed tablets in flood relief camp in Kurnool.
    DECLARATION :
    I here declare that all the information in this document is true and accurate to the best of my knowledge.
    Date :
    Place : (G.SRIKANTH)