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    Senior Clinical Data Science Programmer

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    2+ years
    Not Disclosed
    Bangalore
    10 Oct. 30, 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

    Job Title: Senior Clinical Data Science Programmer - Bengaluru/Chennai, India (Hybrid)

    Company: ICON plc

    About Us: ICON plc is a world-leading healthcare intelligence and clinical research organization. We foster an inclusive environment that drives innovation and excellence. Join us in shaping the future of clinical development!

    Position Overview: We are seeking a Senior Clinical Data Science Programmer with 4+ years of experience in SAS programming. This role involves supporting clinical trials through various data management and programming activities.

    Key Responsibilities:

    • Lead and coordinate programming activities related to clinical data management and analytics.
    • Provide functional knowledge in at least two areas of clinical data science programming, such as data validation, ingestion, extraction, and risk management.
    • Serve as the primary contact during study setup for system programming inquiries.
    • Review database specifications and programs within clinical data management and electronic data capture systems.
    • Build and maintain collaborative relationships with stakeholders to gather business requirements and create specifications for data outputs.
    • Program medium-to-high complexity data ingestion, CDMS outputs, and custom reports.
    • Design cross-page visualization solutions and write scripts in R and Python as needed.
    • Perform data refreshes and track project issues that may affect timelines or budgets.
    • Independently assure the quality of programming outputs and support validation activities.
    • Mentor junior programmers and contribute to a culture of process improvement.

    Qualifications:

    • 4+ years of experience in SAS programming, with a strong understanding of clinical trials and data management concepts.
    • Excellent communication, presentation, and interpersonal skills.
    • Ability to manage multiple tasks and communicate effectively with project teams and management.

    What ICON Can Offer You: Our success relies on the quality of our people. Alongside a competitive salary, ICON provides a comprehensive benefits package focused on well-being and work-life balance, including:

    • Various annual leave entitlements.
    • Health insurance options tailored for you and your family.
    • Competitive retirement planning offerings.
    • Global Employee Assistance Programme for 24-hour support.
    • Life assurance and flexible optional benefits.

    To learn more about our benefits, visit our careers site.

    Diversity and Inclusion: At ICON, diversity, inclusion, and belonging are fundamental to our culture. We are committed to providing an inclusive environment free from discrimination and harassment. All qualified applicants will receive equal consideration for employment.

    If you require reasonable accommodations during the application process, please let us know or submit a request here.

    Interested but Unsure? If you're interested in this role but don’t meet all the requirements, we encourage you to apply—there’s a chance you might be exactly what we’re looking for!

    Current ICON Employees: If you are a current ICON employee, please click here to apply.

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