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SAS Consultant

SAS Consultant

HyqooMalappuram, IN
12 days ago
Job description

Title - SAS Programmer

Type - Contract

Location - Remote

Note - Please apply only if interested for contract role and working hours would be full US PST Hours.

Development and generation of SAS analysis datasets, tables, listings, and graphs from assigned clinical sources; leading development and maintenance of associated operating procedures; and participating in external industry forums (e.g., CDISC, SCDM, and User Groups). This individual performs with minimal on moderately difficult deliverables.

POSITION DUTIES & RESPONSIBILITIES :

  • Utilize programming standards to develop efficient and accurate programs;
  • Support the maintenance of established SAS platform;
  • Support the maintenance a global SAS macro library;
  • Work with Data Management leadership to provide input on reporting processes and standards;
  • Support programming deliverables for clinical trials and support for any custom Data Management reports;
  • Participate in the development and maintenance of global harmonized processes and procedures for programming;
  • Provide quality programming deliverables;
  • Work with BSDM partners, and leadership in Clinical Operations and Franchise to set implement plans for timely delivery of reports, metrics and study deliverables;
  • Facilitate the delivery of standard metric reports;
  • Ability to design, implement and maintain moderately complex programming deliverables across a wide variety of clinical platforms and therapeutic areas

Functional and Technical Competencies :

  • Proficiency in Base SAS, SAS / STAT and SAS Macro language. Advanced SAS certification desirable. Experience programming with R desirable;
  • Demonstrated ability to work in teams to deliver critical milestones;
  • Experience with CDISC datasets, tables , listings and figures desirable;
  • Excellent verbal and written communication skills
  • Leadership Competencies :

  • Connect – Participate in strategic partnerships with Clinical System and Biostatistics at the Enterprise level to ensure MD programming practices meet the needs of the organization
  • Shape – Develop knowledge of therapeutic areas within the Franchises and adapt ADaM and STDM standards for medical devices for use in the MD sector; participate in industry initiatives to define / refine STDM standards
  • Lead – Present opportunities in programming practices that increase quality of deliverables
  • Deliver – ensure high quality programming deliverables for clinical programs are delivered on time and in compliance to regulations and SOPs, seamlessly across all Franchises
  • EDUCATION & EXPERIENCE REQUIREMENTS :

  • A Bachelor’s degree in Statistics , Computer Science or related discipline (required), with at least 6 years of system support in clinical research within Medical Device or Pharmaceuticals .
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