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Sr Sas Programmer

3+ years
Not Disclosed
10 Dec. 17, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Company Overview

Sitero is a leading organization specializing in clinical research and healthcare solutions, dedicated to advancing medical research and improving patient outcomes through innovative technologies and services. As we continue to grow, we are looking for a highly motivated and detail-oriented Senior SQL Reports Programmer to join our dynamic team and contribute to our mission.

Position Overview

The Senior SQL Reports Programmer will provide expert statistical programming and clinical insights in the production of SDTM and AdaM domains, tables, listings, and graphics from clinical trial data. This role will also involve programming Data Management Listings in alignment with sponsor requirements. The ideal candidate will be responsible for preparing, documenting, and testing programs to ensure compliance with regulatory and company standards, while also conducting quality assurance checks. Additionally, the role involves supporting production activities and assisting in training new employees.

Primary Responsibilities

  • Deliver high-quality data to clients (internal and external) by:

    • Developing and executing SAS edit check programs
    • Validating SAS programs following standard validation practices and processes
    • Creating SAS programs to convert data from EDC to protocol-specific SAS datasets according to customer specifications
    • Contributing to the creation of SAS-related project programming and validation documentation
    • Developing SAS macros and format libraries
  • Ensure the quality of clinical data and its export by:

    • Reviewing and approving User Requirement Specifications (URS), Clinical Data Management (CDM) conventions, and working procedure documents
    • Developing and enhancing CDM systems
    • Ensuring the generation of CDISC-compliant datasets
    • Maintaining documentation for customer-specific SAS datasets
    • Assisting with the testing of protocol-specific SAS conversion programs
  • Support project timelines and departmental productivity by:

    • Assessing and assigning target dates for project timelines in collaboration with managers
    • Ensuring adherence to target dates and communicating any necessary changes
    • Coordinating with other departments (operations, study QA, PM, and DM) to ensure departmental efficiency
    • Identifying opportunities to improve departmental procedures and workflows

Secondary Responsibilities

  • Contribute to team success by:

    • Identifying opportunities for process improvement
    • Supporting colleagues and performing additional tasks as required
  • Maintain technical expertise by:

    • Participating in company-sponsored training programs
  • Ensure quality and departmental standards by:

    • Adhering to organizational Standard Operating Procedures (SOPs)
    • Assisting in the creation and enforcement of departmental standards
    • Reviewing and providing recommendations on operational procedures

Qualifications

Education:

  • Bachelor’s degree in Computer Science, Design, or a related field is required
  • An educational background in human-computer interaction, usability, user experience, cognitive science, or applied sciences is a plus

Experience:

  • 8+ years of SAS programming experience in the pharmaceutical industry (required)
  • 5+ years of experience with CDISC, SQL, and relational databases (required)
  • 3+ years of experience in database organization and extracting data to generate listings and reports (required)

Skills:

  • Ability to work independently and within a team setting, adapting to changing priorities
  • Exceptional attention to detail and a commitment to high-quality work
  • Strong interpersonal, verbal, and written communication skills
  • Excellent documentation, organizational, and project management skills
  • Professional demeanor with the ability to maintain a positive and collaborative attitude

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