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September 24th, 2010, 01:25 PM
Post Count Number #1
Moksha Biosciences Hyderabad : CDM SAS Pharmacovigilance Industrial Training
Company Name : mokshabio
Company Location : hyderabad
Designation (of vacancy) : Industrial Training on CDM, SAS AND Pharmacovigilance
Company E-mail ID : cdm@mokshabio.com
Company Website :http://www.mokshabio.com
Job Description, Candidate Profile, Company Profile, Company Address :
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,CDM,SAS AND Pharmacovigilance
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 :
1) CLINICAL DATA MANAGEMENT
2) SAS With Clinical Trails
3) Pharmacovigilance
4) Regulatory Affairs
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
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August 8th, 2011, 04:16 PM
Post Count Number #2
IJT addict
Name : mukesh
Email : mukeshtexv AT gmail.com
Designation / Skillset : fresher
Resume :
Objective
- Seeking a career in a company that provides a competitive environment and an opportunity to learn and develop, both in professional and personal life.
Educational Qualification
- SSLC, VIDYANIKETHAN ENGLISH MEDIUM AND HIGH SCHOOL
Domlur layout
Percentage : 83.04%
- P.U.C Sri M.G.Jain college
Indiranagar.
Percentage : 73.26%
Discipline : PCME
- Bachelor of Technology,
Govt. S.K.S.J.T.I
Bangalore
Aggregate Percentage : 72.2%
Discipline : Textile technology.
Semester University Year of passing Percentage
1st VTU 2008 62.25%
2nd VTU 2008 63.60%
3rd VTU 2009 69.05%
4th VTU 2009 66.82%
5th VTU 2010 66.36%
6th VTU 2010 68.64%
7th VTU 2011 77.82%
8th VTU 2011 78%
Field Of Interest :
- Planning
- Pattern making and designing
- Production field
- Merchandising
- Marketing
Personal Strength :
- Commitment towards work
- Confidence
- Ability to work in Group
- Adjustable to the environment in wherever I work.
- Enthusiastic to learn new concepts.
Declaration :
I hereby declare that all of the above information is correct to the best of my knowledge.
Date :
Place : BANGLORE MUKESH.V
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More Information about this submission and submitter :-
___________________________________________________
Submission ID : 4342968
Date & Time : 7th Jul 2011 3:03 PM (UTC)
IP Address : 122.178.197.236
Browser Info : Mozilla/5.0 (Windows; U; Windows NT 5.1; en-US; rv:1.9.2.3) Gecko/20100401 Firefox/3.6.3
Predicted Country ;: India
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November 23rd, 2011, 12:25 PM
Post Count Number #3
sas resume 3+yrs exp
CURRICULUM VITAE
K. kethana
Email : safireketu AT gmail.com
OBJECTIVE
To obtain a challenging position as SAS Programmer where I can put forth the best of my experiences for the growth of the organization
.
EXPERIENCE SUMMARY
- Over 3.5yrs of Good programming skills in BASE SAS, MACROS, SQL, SAS/STAT, ODS.
- Experienced in proc sql, proc report, proc freq, proc means, proc summary, proc import, proc export and merge statement, Gplot, GChart.
- Good Exposure in SAS functions, procedures, statements, formats, Informats.
- Experienced in generating listing, summary and Pdf reports using SAS Technologies Excellent logical and analytical skills.
- Debug SAS Applications for reduce time management and process
- Relevant exposure to Clinical data management according FDA regulatory authorities
- Good interpersonal, communication and presentation skills.
EXPERIENCE
Organization Designation Duration
Clinnovo Research Labs SAS programmer may’11–Till date
Info Global SAS Mentor Oct’8-oct’11
Vasthalya College of Pharmacy Assistant Professor Oct’9– Dec’10
TECHNICAL SKILLS
- Operating systems : windows (XP , 7, 2000,98)
- Languages : C language
- Analytical Tool : SAS/base, SAS/macros, SAS/GRAPHS
- RDBMS : Sql Server
- Packages : Ms-office, Adobe live cycle
AREA OF INTEREST
- To generate and implement SAS programming for various projects
EDUCATION DETAILS
- Bachelor's Degree in Pharmacy in the year of 2007 from SNVPMV
PROJECT DETAILS
Project #1
Project Title : An eight week, double-blind, randomized, multicenter, parallel group,
Active-controlled study comparing safety and efficacy of therapeutic
Drug in patients with essential Hypertension
Domain : clinical domain
Role : SAS programmer
Environment : SAS/Base, SAS/Macros, sql
Procedures : Report, Transpose, Macros
Responsibilities :
- Extracted data from database using proc sql and created SAS data sets.
- Developed SAS programs for creating intermediate data sets, generating statistical reports as per statistical analysis plan.
- Programs are developed according to specifications of user’s requests and creation of reports for all programs using proc report.
- Developed standard SAS macros to reuse across all clinical studies.
- Performed review and evaluation of clinical research related programs, involved in coding analyzing, report generation and testing programs according to the client requirement.
Project#2
Project Title : A PhaseII, pilot, randomized, placebo-controlled, double-blind study to
Determine safety, tolerability and preliminary evidence of analgesic
Efficacy of drug in patients with third molar extraction dental plan
Domain : clinical domain
Role : SAS programmer
Environment : SAS/Base, SAS/Macros, sql
Procedures : format, sort, merge, Report, Macros
Responsibilities :
- Provided SAS programming and Data base support on conduct & analysis of safety & efficacy of Phase-II studies.
- Developed SAS programs to generate formats and concatenated data using merge.
- Provided SAS programming support on conduct & analysis of clinical trial data.
- Generated reports through macros.
- Process external databases.
- Understand and comply with all SOPs.