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Senior Biostatistician

4-6 years
Preferred by Comapny
11 Nov. 25, 2024
Job Description
Job Type: Full Time Education: PhD in Statistics or related discipline, MS in Statistics or related discipline 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

Role: Senior Biostatistician

The Senior Biostatistician is an integral part of the project team, working independently to deliver high-quality statistical analysis and guidance. This role involves the production, review, and quality control of statistical deliverables while interacting with clients and leading project execution within specified timelines and budgets.


Key Responsibilities

Operational Execution

  1. Project Coordination:

    • Lead project teams to ensure timely and budget-compliant project completion.
    • Act as the primary client contact for statistical and contractual discussions.
  2. Quality Assurance:

    • Perform quality control of derived datasets, tables, figures, and listings.
    • Ensure the accuracy and quality of own work through continuous checks.
  3. Advanced Statistical Application:

    • Apply advanced statistical methods for analyses.
    • Lead production of randomizations, analysis plans, statistical reports, and other documents.
  4. Client Collaboration:

    • Provide statistical data and analysis for Data Monitoring Committee (DMC) reviews.
    • Attend client meetings, contributing to discussions, presenting results, and interpreting findings.

Business Development

  • Actively participate in study design discussions for client and internal meetings.
  • Provide sample size scenarios and statistical expertise during proposal and budget development.
  • Attend and prepare for bid defense meetings for studies and programs.

General Activities

  • Fulfill additional responsibilities as defined by the supervisor or manager.

Required Skills

  • Strong analytical and project management skills.
  • Attention to detail and a professional attitude.
  • Comprehensive understanding of statistical issues in clinical trials.
  • Proficiency in SAS programming.
  • Ability to work independently with good leadership skills.
  • Awareness of business development and matrix team collaboration.

Knowledge and Experience

  • Education:

    • Ph.D. in Statistics or related discipline with relevant experience.
    • Master’s in Statistics or related discipline with 4-6 years of significant experience.
  • Experience:

    • Background in clinical trials or statistical analysis in a similar environment.
    • Knowledge of pharmacokinetic data is advantageous.
  • Language Proficiency:

    • Competency in written and oral English, alongside any local languages.

This position is suited for a motivated professional eager to lead statistical projects, contribute to business growth, and ensure the quality of deliverables while driving clinical trial success.