A new Job, ID: 51570 <http://ejobsville.com/display-job/51570> was
added at eJobsVille.com
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Title:  SAS Inform Programmer  posted on 2013-10-16 12:38:19

Job Description:Position Role:
Team Member – Programmer
Immediate Supervisor:  Team Leader

Job Purpose:
To provide timely quality programming support for eCRF development
activities following relevant GSK processes, procedures, guidelines,
practices and standards. To provide timely feedback to internal and GSK
study team contact, on inefficient or ineffectual processes as identified.


Role and Responsibilities:

eCRF SCREEN BUILD:
* To develop/modify eCRF screens as per specification.
* Unit Test eCRF screens.
* Update the screens based on the feedback from the study team.
* Validation, creation and installation of deployment package in InForm
application.
* Completion of all activities as detailed in the relevant section of
developer checklist.

eCRF CHECK PROGRAMMING:
* To review the Data validation specification (DVS) document for clarity
and to ensure checks are consistent and appropriate based on eCRF design.
Provide feedback to the DVS author.
* Implement standard template checks to meet DVS specifications.
* Create new study specific checks to meet DVS specifications.
* Unit Test eCRF checks.
* Incorporate eCRF checks into study.
* Receive and implement feedback from the execution of the DVS test scripts.
* Update DVS with details of individual data validation checks.
* Completion of all activities as detailed in the relevant section of the
developer checklist.

USER ACCEPTANCE DEPLOYMENT AND ISSUE RESOLUTION :
* Creation of admin files using master user list to assign rights & roles
for user acceptance testing
* Completion of requests for deployment of user acceptance trial for study
team evaluation.
* Update e CRF/ checks based on the feedback from the study team after user
acceptance testing.
* Completion of all activities as detailed in the relevant section of the
developer checklist.

PRODUCTION AND TRAINING TRIAL DEPLOYMENT:
* Creation of admin files using master user list to assign rights & roles
for training & production
* Completion of request for deployment of training and production trails.
* Completion of all activities as detailed in the relevant section of the
developer checklist.

SAS PROGRAMMING
* Review of the DVS for clarity and to ensure checks are consistent and
appropriate based on eCRF design.
* Provide feedback to DVS author.
* Creation and testing for external checks.
* Store files in VSS.
* Completion of all activities as detailed in the relevant section of the
developer checklist.
* Set up of checks in production/ EXACT

InView Automation
* Follow up with data processor / study team leader at TCS for the required
information
* Follow the InView automation checklist points to create a run batch file
& execute on UNIX server
* Inform the study point of contact from data processing at TCS once the
extraction is scheduled
* Review & report any discrepancies

BULK MUL
* Follow up with point of contact from GSK & PhaseForward
* Follow Bulk MUL checklist points to process the MUL & generate admin
files to add new users & sites
* Install test the extract once all the files edited & users/sites added
* Send the admin files generated to PhaseForward to be deployed in the
trial.
* Review & report any discrepancies

Academic Qualification:

Minimum of Bachelors’ degree in a scientific / technical discipline.

Experience:

* 1-3 years of experience in programming (Pharmaceutical Industry) and
familiarity with CDM system is desirable.
* Knowledge/experience of Inform / SAS programming is preferable


Skills required:

* Ability to work across different platforms like SAS, VB, UNIX, and remote
data capture technology
* Effective communication skills. (Verbal and Written).
* Time management skills.
* Collaboration and team work
* Assertiveness in explaining issues and ability to make recommendations
* Effective decision making at a study team level with consultation with
team members and internal Inform programmer (GSK).


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