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    Clinical Programmer

    Gsk Plc
    3-5 years
    preferred by company
    Bangalore
    15 Nov. 22, 2024
    Job Description
    Job Type: Full Time Remote Education: BSc (Bachelor of Science) or BA (Bachelor of Arts) in Mathematics, Statistics, Computer Science, or a related subject. 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 Programmer
    Site Name: UK – London – New Oxford Street, India - Karnataka - Bengaluru
    Location: Bengaluru (Hybrid Mode: 3 days in-office)
    Experience Required: 10-15 years

    Job Purpose:

    The Senior Clinical Programmer at GSK plays a key role in supporting all aspects of programming activities related to clinical trials. This position involves developing, verifying, and documenting analyses of clinical data while adhering to study protocols, analysis plans, and GSK/industry standards. Senior Programmers are expected to mentor and train junior team members, engage in study lead activities under supervision, and support the planning and execution of programming activities.

    Key Responsibilities:

    Programming Expertise:

    • Demonstrate proficiency in developing, QCing, and debugging complex code and macros with minimal supervision.
    • Identify gaps in current programming best practices and offer suggestions for improvement.
    • Ensure adherence to internal and external standards, with an awareness of evolving programming standards.
    • Implement internal processes and standards for accurate, high-quality deliverables within agreed timelines.
    • Proactively anticipate problems related to assigned work and implement solutions with input from colleagues as needed.
    • Contribute to programming best practices and provide innovative solutions for complex problems.
    • Perform Quality Control (QC) of others' work under supervision and ensure compliance with GxP and ICH requirements.

    Leadership & Collaboration:

    • Participate in strategic planning under supervision and collaborate with stakeholders.
    • Engage in cross-functional collaborations, providing input on safety issues and processes.
    • Lead programming aspects of a study, while interacting with non-programming team members.
    • Present technical approaches to peers and non-technical colleagues, both in internal forums and external professional settings.
    • Mentor junior programmers and new hires, providing training and guidance where required.

    Documentation & Compliance:

    • Ensure all documentation is accurate, timely, and archived as per regulatory standards.
    • Anticipate compliance, quality, or governance issues and propose solutions for resolution.
    • Contribute to process improvement initiatives and maintain awareness of departmental strategies.

    Qualifications & Skills:

    Required:

    • A BSc or BA (or equivalent) in Mathematics, Statistics, Computer Science, or a related subject.
    • Experience or knowledge of programming languages such as R, Python, Spotfire, S-Plus, and/or SAS.
    • Intermediate to advanced programming skills in one or more languages (R, Python, SAS).
    • Familiarity with CDISC standards and their application.
    • Basic knowledge of Microsoft Office (MS Word, Excel, PowerPoint, Outlook).

    Preferred:

    • Experience with submission activities.
    • Intermediate to advanced understanding of the end-to-end clinical trial process.
    • Strong understanding of the purpose and application of key clinical documents.
    • Experience representing the programming function in cross-functional meetings and initiatives.
    • Some experience in training and mentoring junior programmers.
    • Therapeutic area expertise, preferably in Oncology.

    Why GSK?

    At GSK, we aim to positively impact the health of 2.5 billion people over the next 10 years. Our commitment to R&D and the development of transformational vaccines and medicines drives us to revolutionize the way we approach medical discovery. By uniting science, technology, and talent, we are advancing the field of clinical research and improving patient outcomes globally.

    Closing Date for Applications: November 22, 2024

    Please ensure to attach your cover letter or CV when applying, describing how you meet the competencies for this role. The information provided in these documents will be used to assess your application.

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