Sr SAS Programmer - Bengaluru / Bangalore - Thepharmadaily

    Thepharmadaily
    Thepharmadaily Bengaluru / Bangalore

    1 week ago

    Full time
    Description

    rimary Responsibilities

    • Data Provision to Clients
    • Create and execute SAS edit check programs .
    • Validate edit check programs using standard validation practices and processes.
    • Develop SAS programs to convert data from EDC systems to protocol-specific SAS datasets according to customer specifications.
    • Assist in the creation of SAS-related project programming and validation documentation.
    • Develop SAS macro and format libraries.
    • Data Quality Assurance
    • Review and approve User Requirement Specifications (URS) , Clinical Data Management (CDM) conventions, and related documents.
    • Develop and implement new CDM systems or enhancements to current systems.
    • Ensure the creation of CDISC-compliant datasets .
    • Generate documentation for customer-specific SAS datasets.
    • Maintain the SAS environment, providing assistance with SAS installation , updates, and maintenance.
    • Project Management Support
    • Collaborate with the Study Quality Representative to test protocol-specific SAS conversion programs.
    • Assess and assign target dates for project timelines, adhering to these dates in conjunction with your manager.
    • Communicate any changes in project timelines to the Project Manager and other relevant personnel.
    • Keep department heads informed of ongoing project issues.
    • Process Improvement Efficiency
    • Coordinate activities between the Clinical Programming department and other related departments (Operations Programming, Study QA, PM, and DM) for improved efficiency.
    • Evaluate current procedures and work instructions, recommending improvements to achieve departmental objectives.
    • Assist the Training Department in developing and maintaining training materials for Clinical Programming.

    Secondary Responsibilities

    • Team Collaboration
    • Explore new opportunities to add value to departmental processes and the organization as a whole.
    • Support team members in achieving goals and contribute to team success.
    • Perform additional duties as assigned and deemed necessary.
    • Technical Knowledge Continuous Learning
    • Participate in applicable company-sponsored training programs to maintain and expand technical expertise.
    • Maintaining Standards Quality
    • Read, understand, and adhere to organizational Standard Operating Procedures (SOPs) .
    • Assist in establishing and enforcing departmental standards.
    • Provide recommendations on operational procedures and actively engage in process improvement initiatives.

    Qualifications

    Education

    • Bachelor s degree in Computer Science , Design , or a related field.
    • Educational background in Human-Computer Interaction , Usability , User-Centered Design , User Experience , Information Design , Applied Psychology , Cognitive Science , Human Factors , Informatics , or other design/applied science fields is a plus.

    Experience

    • 8+ years of SAS programming experience in the pharmaceutical industry.
    • 5+ years of experience working with CDISC , SQL , and Relational Databases .
    • 3+ years of experience with database organization and the ability to extract data to generate listings and reports.

    Additional Skills

    • Ability to work both independently and as part of a group.
    • Strong attention to detail and a meticulous approach to work.
    • Excellent communication skills, both verbal and written.
    • Strong documentation and organizational skills.
    • Professional and positive attitude with a focus on maintaining high standards
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