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Clinical SAS, SDTM programmer

Location:
India
Posted:
February 20, 2018

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Resume:

Name : Sridevi Vishwagna

Email : ac4jjh@r.postjobfree.com

Contact no. : +91-830*******

KNOWLEDGE, SKILLS AND ABILITIES:

•Clinical Data Programming: Good knowledge of Oracle and/or SAS.

•Solid understanding of clinical drug development process.

•Excellent organizational, communication, and technical database skills

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

PROFESSIONAL EXPERIENCE:

IQVIA SERVICES PVT. LTD. (FORMER- QUINTILES) Bangalore, India May 2017-Present

Designation: Programmer Analyst, Clinical Data Programming

Responsibilities:

•Plan and coordinate database design, development, implementation, maintenance, and user support of clinical systems.

•Provide technical expertise in conjunction with internal and external clients.

•Program, test, and document databases in accordance with programming standards and validation procedures.

•Program database manipulation and transfers of data for internal and external clients.

•May assist IT in developing and implementing new technologies.

•May assist IT in testing and evaluating new upgrades to technologies.

•May assist in developing, revising, and maintaining core operating procedures and working instructions.

•Meet objectives as assigned, and interact with the project team to organize timelines, responsibilities and deliverables.

•Develop and maintain good communications and working relationships with teams and external clients.

•May interact with corporate team and CDM team members to negotiate timelines, responsibilities, and deliverables.

•May serve as Lead Programmer on the corporate team.

ACCENTURE SERVICES PVT. LTD. Bangalore, India December 2013-April 2017

Designation: SDTM Sr. Associate

Responsibilities:

•Review and analysis of source (raw) data.

•Author mapping specifications from source (raw) data to target (CDISC SDTM and/or sponsor defined standards).

•Develop CDISC SDTM domains utilizing SAS, PL/SQL and data conversion tool.

•Quality Control of CDISC SDTM domains.

•Assist with project status report and project related documentation.

•Proactively identify issues and contribute to solutions.

•Ensure quality for internal and external deliverables.

•Additional responsibilities as assigned or required.

IDDCR PVT. LTD. Hyderabad, Telangana May 2012-December 2013

Designation: Clinical SAS Programmer

Responsibilities:

•Importing excel sheets using SAS.

•Creating tables and listings using different procedures and functions.

•Creating SDTM standardized datasets using SAS.

•Perform domain level, variable level, value level mapping.

•Standardizing all the created datasets according to CDISC SDTM v3.1.2

REWARDS AND RECOGNITION:

•Recognition Award: Received for excellent quality work and managed to deliver multiple studies in the specified time line.

•PACE Award: Received for Delivery Excellence.

•NUMERO UNO: Handling multiple studies at a time. Meeting timelines consistently with 100% quality.

•Bravo Award: Conducting training sessions on base SAS certification and gaining positive feedback.

•Applause Award: Pitching in one of the trial activities at the crunch time and completed within 2 days timeframe. For coordination and team work.

COMPUTER SKILLS:

•SAS / BASE, SAS/ADVANCED,MACROS, SQL

•Oracle Clinical/ PL SQL

•Oracle Argus

•MS Office

•C language

EDUCATION/TRAINING:

•B.Tech, Biotechnology, Sree Nidhi Institute of Science and Technology, Hyderabad, Telangana, 2011.

•Base SAS Certified Programmer, June, 2013.

•Advanced SAS Certified Programmer, June, 2015.

DECLARATION:

I hereby declare that the information furnished above is correct and true to the best of my knowledge.

PLACE : Bangalore (V.SRIDEVI)



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