Jobs Career Advice Signup
X

Send this job to a friend

X

Did you notice an error or suspect this job is scam? Tell us.

  • Posted: Nov 14, 2023
    Deadline: Not specified
    • @gmail.com
    • @yahoo.com
    • @outlook.com
  • Never pay for any CBT, test or assessment as part of any recruitment process. When in doubt, contact us

    IQVIA, formerly Quintiles and IMS Health, Inc.,is an American multinational company serving the combined industries of health information technology and clinical research. It is a provider of biopharmaceutical development and commercial outsourcing services, focused primarily on Phase I-IV clinical trials and associated laboratory and analytical services,...
    Read more about this company

     

    Senior / Principal Statistical Programmer (m/w/d)

    Job duties:

    • Development of study outputs including SDTM/ADaM datasets, tables, listings, figures and QC of requested output.
    • Participate in the design, development and quality control process for SAS programs used to access, extract, transform, review, analyze and submit clinical data for all requested analyses.
    • Interact with internal departments of the sponsor - Biostatistics, Data Management, Regulatory Operations and Medical Writing.
    • Collaborates with peers and statisticians to ensure the submission readiness of clinical data as required by authorities (i.e. SDTM, ADaM, tables, figures, listings, define.xml).
    • Involvement with creation and maintaining programming specifications for SDTM, ADaM and integration of data in support of ISS/ISE.
    • Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group.
    • Perform additional statistical analyses including but not limited to: support responses to regulatory agencies; generate integrated summary of safety and efficacy; support publications and presentations; support planning and reporting of clinical trials via exploratory analyses of available data; replicate vendor and statistician analyses for QC.

    Our expectations of you:

    • 5 years or more in SAS programming for clinical trial data.
    • Bachelor’s degree in Math, Stats, Computer Science, Pharmacy, Biology or related.
    • Strong knowledge in CDISC standards (SDTM, ADaM).
    • Knowledge in the creation of define.xml, Pinnacle 21, aDRG, and sDRG.
    • Knowledge of pharmaceutical clinical development - understanding of safety deliverables and efficacy analysis supporting regulatory submissions.
    • Knowledge of base SAS, proc report, exposure to macros, current CDISC data structures, and standardization methodology; demonstrated ability to debug SAS programs.
    • High degree of technical competence in SAS Macro programming, SAS SQL, XML, RTF, and PDF.
    • Demonstrated teamwork, pride of ownership, accountability, problem-solving and innovative skills.

    Method of Application

    Interested and qualified? Go to IQVIA on jobs.iqvia.com to apply

    Build your CV for free. Download in different templates.

  • Send your application

    View All Vacancies at IQVIA Back To Home

Subscribe to Job Alert

 

Join our happy subscribers

 
 
Send your application through

GmailGmail YahoomailYahoomail