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    Senior Programming Associate / Programming Manager

    Genmab
    2+ years
    $76.500,00---$127.500,00
    Remote, USA
    10 Aug. 16, 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

    About Genmab

    At Genmab, our mission is to build extraordinary futures together. We are dedicated to developing cutting-edge antibody therapies that transform the lives of patients and revolutionize the future of cancer treatment and other serious diseases. Our commitment is reflected in our innovative, science-driven approach and our team’s values of authenticity, excellence, and impact.

    The Role

    Position: Senior Programming Associate / Programming Manager
    Location: Princeton, NJ, USA; Copenhagen, Denmark; or Utrecht, the Netherlands (Hybrid)

    The Senior Programming Associate / Programming Manager plays a crucial role in supporting the development of new therapies by ensuring the integrity, consistency, and adherence to data standards. You will work closely with the Lead Programmer and collaborate with various departments, including Data Management, Statistics, Drug Safety, Medical, Clinical Pharmacology, and Biomarkers. Your primary responsibilities will include:

    Responsibilities

    • Data Review & Standards:

      • Review CRFs for adequacy and consistency.
      • Support the establishment and maintenance of Genmab’s SDTM and ADaM database standards.
      • Perform consistency checks on databases delivered by preferred vendors.

    • Programming & Analysis:

      • Develop and write SAS or other programs to produce well-structured data summaries, tables, figures, and listings for various deliverables, including regulatory submissions and internal reports.
      • Aid in sponsor oversight of programming activities and perform QC on SAS code written by colleagues.
      • Support resource planning and outsourcing of programming activities.

    • Collaboration & Support:

      • Collaborate with Data Management, Statistics, and other departments to support cross-functional projects.
      • Contribute to process improvements and knowledge sharing within the team.
      • Maintain up-to-date knowledge of relevant regulatory guidelines and therapeutic areas.

    Requirements

    • Education & Experience:

      • Bachelor’s degree or equivalent in a relevant field.
      • Minimum of 2 years of experience in the pharmaceutical industry as a Programmer (for Senior Programming Associate level).
      • Experience with SAS, R, and Python programming languages.

    • Skills:

      • Proficiency in CDISC, SDTM, and ADaM data models.
      • Strong analytical and problem-solving skills.
      • Ability to write efficient, well-documented programs and maintain high-quality standards.
      • Effective communication and teamwork abilities.
      • Proactive, accountable, and goal-oriented with a flexible approach to managing multiple tasks.

    About You

    You are passionate about Genmab’s mission to innovate cancer treatment and improve patient lives. You bring rigor and excellence to your work and thrive in a dynamic, fast-paced environment. You excel in collaboration and knowledge sharing, and you are committed to continuous improvement and innovation.

    Locations

    This role is based in Genmab's offices in Princeton, NJ; Copenhagen, Denmark; or Utrecht, the Netherlands, with hybrid work options available. Remote work may be considered, preferably for candidates in Eastern or Central Time Zones (US) or European time zones.

    Application & Salary

    Please apply by February 12, 2024. For US-based candidates, the proposed salary range is $76,500 to $127,500, with additional compensation such as bonuses potentially available. Actual salary offers will consider skills, qualifications, experience, and location.

    Diversity & Inclusion

    Genmab is committed to diversity, equity, and inclusion at all levels of the company. We value and respect diverse backgrounds and strive to ensure fairness and equal opportunity for all applicants. Learn more about our commitment to diversity on our website.

    Privacy

    Genmab is dedicated to protecting your personal data and privacy. Please review our privacy policy on our website for details on how we handle your application data: Genmab Privacy Policy.

    Note: In the Netherlands, Genmab initially offers a fixed-term employment contract for one year, with the possibility of renewal for an indefinite term based on performance and business conditions.

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