Wednesday, 9 November 2016
Wednesday, 2 November 2016
Hiring Drive Clinical Database Programmers
Any of the following Database Programming Expertise :
1. OCRDC
2. RAVE
3. INFORM.
Expectations:
With general direction, develop and maintain all standard objects, procedures, templates and views for clinical database management system (such as OC/RDC, Inform, Rave) using relevant programming languages (SQL, PL/SQL, C #, VB script, SAS) standard Global Library. With guidance, translate data models into metadata specifications for inclusion into the Metadata Repository .
With general direction begin to assist more experienced CSA in the interpretation of data collection requirements and the creation of data models of low to moderate complexity
Ideal Background :
Minimum 2 years and up to 10 yrs. clinical database programming,
With general direction, develop and maintain all standard objects, procedures, templates and views for clinical database management system (such as OC/RDC, Inform, Rave) using relevant programming languages (SQL, PL/SQL, C #, VB script, SAS) standard Global Library. With guidance, translate data models into metadata specifications for inclusion into the Metadata Repository .
With general direction begin to assist more experienced CSA in the interpretation of data collection requirements and the creation of data models of low to moderate complexity
Ideal Background :
Minimum 2 years and up to 10 yrs. clinical database programming,
setup of clinical databases and CRF design experience gained in the pharmaceutical industry or CRO as well as the following:
Basic CDISC Understanding: Implementation of CDISC Standards (SDTM).
Good Understanding of clinical data management systems and/or relational databases as applied to clinical trials: Input to requirements for eCRF Development.
Good knowledge of (SQL, PL/SQL, C #, VB script, SAS): Development of validation and derivation procedures.
Ability to translate technical concepts for non-technical users in the areas of CRF and validation procedure implementation in CDMS
Basic CDISC Understanding: Implementation of CDISC Standards (SDTM).
Good Understanding of clinical data management systems and/or relational databases as applied to clinical trials: Input to requirements for eCRF Development.
Good knowledge of (SQL, PL/SQL, C #, VB script, SAS): Development of validation and derivation procedures.
Ability to translate technical concepts for non-technical users in the areas of CRF and validation procedure implementation in CDMS
Mail your application across Naresh_kumar.gunda@Novartis.com
Novartis is Hiring for Hyderabad based Vacancies from Mumbai on 04 Nov 2016 and From Bangalore on 11 Nov 2016.
Interview Venue details will be sent to the shortlisted applicants.
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