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    Senior Statistical Programmer- Fsp- Permanent-Remote

    Cytel
    5+ years
    Not Disclosed
    Remote, USA
    10 Aug. 6, 2024
    Job Description
    Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, 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

    Senior Statistical Programmer

    About Cytel:

    Cytel offers unparalleled expertise in biostatistics and operations research to life sciences industries through innovative software and services. At Cytel, we focus on fostering professional growth and creating successful careers for our employees, which in turn drives our own success. We are a dynamic environment where talent, experience, and integrity converge to advance clinical development.

    Role Overview:

    As a Senior Statistical Programmer, you will work under the direction of the Principal Programmer, conducting programming activities for trials, early-phase projects, indications, or publication activities. You will lead and guide at least one study team, and may manage a team of 2-4 members. Your responsibilities will include data migration, SAS programming, and ensuring high-quality delivery of analysis datasets and reports.

    Key Responsibilities:

    • Lead and provide technical and domain-related guidance to at least one study team; may manage a team of 2-4 members.
    • Perform data migration from legacy datasets to CDISC or other client-specific standards.
    • Read and understand program specifications documents.
    • Prepare SAS analysis datasets, tables, listings, and figures according to specifications.
    • Create programs to generate graphs and tables for Clinical Study Reports (CSRs), safety reports, efficacy reports, etc., ensuring timely and high-quality delivery.
    • Validate and transform datasets, tables, listings, and figures as per client specifications.
    • Coordinate with clients and the US team to clarify specifications, resolve data issues, manage outliers, and adhere to schedules.
    • Contribute to the recruitment process by identifying resource needs, conducting interviews, and hiring appropriate candidates.
    • Adhere to standard operating procedures (SOPs) as defined in the Quality Management System or by respective clients.

    Qualifications and Experience:

    • Bachelor's or Master’s degree in Computer Science, Statistics, or a related health science field.
    • Minimum of 5 years of SAS programming experience with clinical trial data.
    • Required experience with CDISC standards.
    • Strong understanding of regulatory requirements and the drug development process.
    • Solid knowledge of the clinical trial domain and proficient SAS programming skills.
    • Ability to work independently and manage multiple tasks effectively.

    Why Cytel?

    • Career Growth: We offer competitive compensation, a comprehensive benefits package, and opportunities for professional development.
    • Work Environment: Benefit from a collaborative and innovative workplace with a focus on results.
    • Diversity & Inclusion: Cytel is an Equal Employment / Affirmative Action Employer. We consider all applicants without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity, or any other protected characteristic.

    Important Notice:

    Cytel does not accept referrals from employment businesses or agencies for vacancies posted on this site. All employment businesses or agencies must obtain prior written authorization from Cytel’s human resources department before referring candidates. Unauthorized referrals will not incur any liability or fees for Cytel.

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