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Sr. Clinical Programmer Analyst Resume

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Alameda, CA

SUMMARY:

  • More than 10 years working on Clinical Trials with Phase I, II, III & IV study.
  • More than one year working on CDISC SDS ADAM data sets generating and maintaining.
  • More than two years working with Regulatory FDA submission
  • Using SAS/AF etc. develope one Application that can be used to support Clinical Data Collect and Data Clean activities
  • Good working knowledge of more than one programming tool and usually work on more than one platform.
  • Ability to work independently or under direct supervision, but typically assumes independent task management responsibility.
  • More then 10 year experience in SAS/AF, SAS/FSP, SAS/BASE. SAS/STAT, SAS/GRAPH;
  • Broad knowledge of computer language: BASIC, FORTRAN, dBase, and familiar with C/C++.
  • Outstanding quantitative & analytical skill.

EXPERIENCE:

Sr. Clinical Programmer Analyst

Confidential, Alameda, CA

Responsibilities:

  • Provide SAS programs for all Tables and Listings for clinical studies according to Statistical Analysis Plan (SAP) using Phase 1 & Phase 3 data.
  • Perform Ad Hoc analyses of data as needed by the Company.
  • One of major team member to do SAS Serve Soft Ware instillation and IQ, PQ, OQ.
  • Using SAS/AF, FSP, Base, STAT, & Graph etc. developed one Application that can be used through the whole Clinical Data Collection; i.e. start from 1.
  • Patient Enrollment, 2. CRF Data Entry Form Design, 3.
  • Initialize Data Sets depended on Protocol and SAP with Audit Trial Set Up, 4. CRF Receiving, 5.
  • Using Data Entry Form to do double Data Entry, 6. DCF (Data Clarify Form) or Query/Tracking create, 7. Primary & Secondary Data Entry Comparison, 8.
  • Edit Check, 9. Data Edit with 5 Data change reason (Data Entry Error, Edit Check Error, Audit Error, Self Evident Correction, Site Initialized Correction), all the change will be automatically recorded in Audit Trial, 10.
  • Created MedDRA auto coding function .

Sr. SAS Programmer

Confidential, Indianoplis, IN

Responsibilities:

  • Work with Statisticians, Programmers, Medical doctor etc.
  • Using SAS, MS tool to create SAS analysis databases, summary tables and graphs for presentations, manuscripts and reports.
  • Write and document SAS production macro code.

SAS Programmer

Confidential, San Francisco, CA

Responsibilities:

  • Provide SAS and other programming support with respect to design, conduct & Analysis of clinical trials.
  • Create SAS analysis databases, summary tables and graphs for presentations, manuscripts and reports.
  • Write and document SAS production macro code that can be used for a wide variety of applications.
  • Develop SAS programs for statistical tables, data listings, and edit checks.
  • Assist with Programming for editing and quality control of clinical trial data.
  • Documentation of all SAS production code.
  • Review CRFs, Data Management and Analysis Plans.
  • Serve as the lead on a programming team. It will be the responsibility to ensure that work has been distributed appropriately and that all tasks are completed accurately and on time.

Sr. Stistical Programmer

Confidential, Baltimore, MD

Responsibilities:

  • Work with Statisticians, Programmers, Medical doctor etc.
  • Using SAS, Microsoft Word, EXCEL R etc. to do Safety and Efficacy TLG for CSR, NDA, BLA.
  • Using SAS and other software to do CDISC SDS & ADAM data set generating and maintaining, data mining & data manipulating.
  • Some QC & Documentation.

Sr. Stistical Programmer

Confidential, Rockville, MD

Responsibilities:

  • Work with Statisticians, Programmers, Data Management Analysts;
  • Using SAS, Microsoft Word, HTML etc. to do Safety TLG for CSR, NDA, BLA.
  • Using SAS and other software to do data transfer, data mining, & data manipulating.
  • QC & Documentation.

Sr. Stistical Programmer

Confidential, Lexington, MA

Responsibilities:

  • Work with Statisticians, Programmers, Data Management Analysts, Regulatory staff and Medical
  • Using SAS and other software to do data mining, data warehouse maintaining and exterior data convert to SAS data or vice verse.
  • Using SAS to do Subject Auditing, Safety and Efficacy Auditing, and Data Edit Auditing.
  • Using SAS, Microsoft Word, EXCEL etc. to do Subject Audit Documentation, Safety and Efficacy Audit Documentation and Data Edit Audit Documentation.
  • Using SAS to do table, listing & figure generation for FDA submission.
  • Work with Statisticians Data analysts or other programmers in building or analyzing data files or providing survey support services.
  • To do initiate and analyze, evaluate, test and code programs.

Sr. Statistical Programmer

Confidential, Foster City, CA

Responsibilities:

  • Working with statisticians, Data coordinator, and Medical Doctor, and using SAS and some other software through Window NT to do data transfer, validation, edit check, data mining, and data warehouse maintain; generating the report and documentation for some clinical trial project.
  • Some QA/QC job.

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