Clinical SAS programmers walk-in drive

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,
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


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.

Walkin SAS Programmers and Clinical Data analyst

 Learn how to manage Clinical data

Walkin - Clinical SAS Programming (cdp/clinical Domain)

Eligibility:

Good Communication
Solid understanding of clinical domain,experience on Clinical SAS Programming ( Experience in Clinical Domain Mandatory ) (Working large data)
Excellent organizational, communication, and technical database skills 
Ability to establish and maintain effective working relationships with coworkers, managers and clients 

Interested candidates can walk-in to our Mumbai Office Thane on 
1-Oct-2016 Timing 8:30 AM,  send their Resume to naveen.alexander@quintiles.com


Company : 
+Quintiles 
Address :
G Corp Tech Park, Next to Hypercity Mall, Ghodbunder Rd, Thane-400601, Maharashtra 

Walkin - Clinical SAS Programming

Eligibility:

Good Communication
Experience in Clinical Domain - Mandatory 
Solid understanding of clinical domain,experience on #Clinical #SAS #Programming  - Mandatory 
Excellent organizational, communication, and technical database skills 
Ability to establish and maintain effective working relationships with coworkers, managers and clients 

Interested candidates can send their Resume to naveen.alexander@quintiles.com and can 

Walkin on 17-Sept-2016


Timing - 8:30 AM


Address - 
+Quintiles 
Prestige Technology Park II, 
Etamin Block B Wing 1st Floor ,
Sarjapur-Marathahalli ,
Outer Ring Road ,Bangalore 560 103 India

Walk in Drive for Clinical SAS Programmers

Job location  : Hyderabad.


1.Statistical Programmer       -      3 - 5 Years
2.Senior SAS Programmer    -      5 - 8 Years
3.Lead  / Principal SAS Programmer    -     8+ Years


Job Description:Locally coordinate and take responsibility for trial level programming activities (analysis datasets, pooled datasets, listings, tables and figures) of individual Phase I-IV clinical trials to support program programmers and statistician in project level activities.
Be responsible for statistical tasks on assigned clinical trials e.g. RAP.
Maintain efficient interfaces with internal and external customers with support of ONC Biometrics management and the Program Programmer/Statistician.
Make certain that documents and specifications are consistent and comply with company standards by providing input into CRF and data structures tables, listings and figures for phase I-IV clinical trials and submission activities.
Program and deliver, according to specifications, analysis datasets, pooled datasets, listings, tables, and figures for phase I-IV clinical trials and for pooled analysis with high quality and within milestones.
In consultation with the statistician, develop specifications for analysis datasets, pooled datasets, and listings
Maintain records for all assigned projects and archiving of trial / project analysis and associated documentation.
Provide input on process improvement initiatives and participate in non-clinical project activities with support from GH

NOTE:   Only the shortlisted applications are invited for the drive


Walk-in date : 26th Aug


Reach undersigned or drop  a note for more details 
Naresh Kumar.Gunda
040-67581684.
Naresh_kumar.gunda@Novartis.com

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