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    Senior / Principle Statistical Programmer

    Clinovo
    3-5 years
    Preffered by Company
    Remote
    10 Aug. 29, 2024
    Job Description
    Job Type: Full Time Education: B.Pharm/ M.Pharm/ B.Sc/ M.Sc/ Any LifeScience 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 Statistical Programmer

    Company Overview:

    Clinovo is dedicated to empowering healthcare and life science companies by connecting them with top clinical research professionals. Our proven track record spans pharmaceutical, biotechnology, diagnostic, medical device, and CRO sectors. Clinovo is the trusted partner of leading companies due to our exceptional customer service, quality candidate profiles, and long-term relationships.

    Position Summary:

    Our esteemed client is seeking a highly skilled and motivated Senior Statistical Programmer to develop and implement process methodologies that address both internal and external client needs. This role involves planning and coordinating the development of integrated programming solutions for a wide range of statistical programming requirements. The position will provide technical leadership and internal consulting services, including developing specifications and analyzing user needs for complex projects or client requirements.

    Key Responsibilities:

    • Plan, coordinate, and execute programming tasks for complex studies, including:
      • Programming, testing, and documenting statistical programs for creating tables, figures, and listings.
      • Programming analysis datasets (derived datasets) and transfer files for internal and external clients.
      • Performing quality control checks on source data and reporting data issues as needed.
    • Interpret project-level requirements and develop detailed programming specifications for complex studies.
    • Offer advanced technical expertise and solutions to internal and external clients, handling complex projects effectively.
    • Serve as the technical team lead for individual complex studies or groups of studies.
    • Communicate directly with internal and client statisticians and clinical team members to ensure clarity on requirements and project timelines.
    • Estimate the scope of programming work, manage resource assignments, communicate project status, and negotiate or renegotiate timelines as needed.
    • Utilize and promote established standards, SOPs, and best practices.
    • Provide training and mentoring to Statistical Programming (SP) team members and department staff.

    Preferred Skills and Experience:

    • Extensive experience with statistical programming in SAS within the CRO/Pharmaceutical/Biotechnology/Healthcare industries.
    • Proven experience as a technical team lead, engaging directly with clients and coordinating tasks within a programming team.
    • In-depth knowledge of clinical research regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
    • Advanced understanding of statistics, programming, and/or the clinical drug development process.
    • Proficiency in Base SAS, SAS/STAT, SAS Graph, and SAS Macro Language.
    • Strong organizational, interpersonal, leadership, and communication skills.
    • Ability to independently manage multiple tasks and projects.
    • Skill in delegating work and mentoring SP team members.
    • High attention to detail and accuracy.
    • Competence in solving routine and complex problems.
    • Ability to lead teams and manage projects effectively.
    • Strong capability to establish and maintain productive working relationships with colleagues, managers, and clients.

    Requirements:

    • Master’s degree in Computer Science or a related field with 3 years of relevant experience; or
    • Bachelor’s degree in Computer Science or a related field with 5 years of relevant experience; or
    • Equivalent combination of education, training, and experience.

    Location: Remote

    Compensation: Commensurate with experience, skills, and qualifications.

    Clinovo is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

    If you are passionate about making a difference and possess the skills and experience we are looking for, we encourage you to apply!

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