Featured post

Where the Nervous System findings go?

Check out video version of this topic

Monday 3 November 2014

Walk-in for team member Quality -global MNC

Check quality of medical reports
Fraud detection
Training of diagnostic centres

Eligibility:
Any Graduate / Post Graduate
Self-motivated and results-driven
Excellent communications skills - writing, oral, presentation


Walkins dates: From 3rd November to 7th November 2014 from 10.00 am to 5.00 pm

Readmore:

https://www.linkedin.com/groups/Global-Pharma-Science-Network-6731934/about

Tuesday 21 October 2014

Walk-ins for CDA for freshers with global MNC



Eligibility:

Bachelors degree/post graduate  in clinical or life science background


Medical terminology exposure

Excellent organizational, communication and computer skills

Ability to exercise excellent attention to detail

Ability to act independently and with initiative required to resolving problems

Ability to establish and maintain effective working relationships with coworkers, managers and clients

Experience:

0-2yrs


Sunday 19 October 2014

1day to go-Walk-ins for freshers for Pharmacovigilance with global MNC

Experience: 

B-Pharm Freshers 0-3 months experience 

Skills: .Good Communication skills (Written & Verbal)
. Good Analytical skills.

Sunday 21 September 2014

How to submit ‘NOT DONE’ and ‘NONE’

If group of tests or an individual test is ‘not done’ and the information is captured on CRF, it should be indicated in corresponding dataset


On the other hand, if there is no information for group of tests or an individual test whether it is done/yes/no/not done or data on CRF is missing, a record must not be created to indicate that data was not collected.

Sunday 24 August 2014

Walk-ins for Life science grads/freshers as project assistants with leading research based organization

Qualification : MSc microbiology/biochemistry/Biotechnology/Organic Chemistry/Chemistry
B tech/M tech Chemical engineering
M tech Biotechnology
M tech nanotechnology

Wednesday 11 June 2014

TYPES OF CONTROLLED TERMINOLOGY(CT) IN CDISC SDTM

  •  Single asterisk(*) – Specifies there is no CT currently, sponsor defines their own CT while CDISC team may be developing one
         Ex: Variables in DM domain

Variable name
Label
Type
Controlled terminology
Role
ARMCD
Planned arm code
Char
*
Record qualifier
ARM
Description of planned arm
Char
*
Record qualifier


Friday 2 May 2014

Pharmacovigilance opening at Crest..

identifying and evaluating individual case safety reports (ICSRs) of adverse drug reactions from the published literature 
creating summary content in a range of formats (narrative summaries, structured database inputs, electronic formats for regulatory filing ) to support the drug safety reporting and information requirements of pharma industry clients

Thursday 1 May 2014

University of Hyderabad is Hiring..

Applications are invited for the following posts.
Project Assistants (PA): 02 PostsQualification:M.Sc. (Organic Chemistry)/ those who have appeared for the semester final examination upon completion of previous semesters are also eligible.

Monday 28 April 2014

THE SDTM STANDARD DOMAIN MODELS


They are about 46 domains of which 32 clinical data domains are contained into Interventions, Events and Findings.Six domains for trial design and four domains for special purpose.

Friday 25 April 2014

SDTM DATA CLASSES

Describes the datasets or domains within SDTM. These are of six types as follows
General observation Classes:
Subject level observations collected during the study goes into one of three general observation classes as follows

Wednesday 23 April 2014

SDTM(Study Data Tabulation Model): An Introduction (continued)

SDTM BASIC CONCEPTS:
Of the numerous standards developed by CDISC, this blog focus on one of the standards i.e SDTM.SDTM is defined   with  two key documents-The Study Data Tabulation Model, and the SDTM Implementation Guide(SDTMIG).