ImmunityBio, Inc.

Senior Statistical Programmer

ImmunityBio, Inc.

full-time

Posted on:

Location Type: Remote

Location: CaliforniaUnited States

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Salary

💰 $135,000 - $150,000 per year

Job Level

About the role

  • Lead all aspects of statistical programming activities inclusive of creation, validation, traceability, reproducibility, and maintenance of analysis datasets and statistical outputs.
  • Contribute to and review statistical analysis plans and analysis datasets specifications.
  • Prepare the electronic submission of clinical trial data to regulatory authorities.
  • Anticipate statistical programming resource needs and work with management to ensure adequate long-term resource allocation within a project.
  • Provide effective solutions for complex statistical programming tasks.
  • Provide input or lead data standardization efforts (e.g., CRF and database design, edit checks, standard statistical programs, data presentations, data standards such as CDISC STDM/ADaM, and e-submissions).
  • Create and manage project and study electronic subdirectories ensuring consistency in structure.
  • Contribute to the design, creation, and validation of global programming macros that streamline programming activities and increase efficiency.
  • Participate in development of new processes or revision of existing processes.
  • Keep current with new statistical programming techniques and technical advancements.
  • As necessary, provide work direction, guidance, mentoring, influence and support to junior staff.
  • Train junior staff in more complex statistical programming techniques.
  • Adhere to Standard Operating Procedures (SOPs), process improvements, and standardization of templates.
  • Perform ad-hoc and cross-functional projects assigned to support business needs and provide developmental opportunities.

Requirements

  • Bachelor’s Degree in Statistics/Biostatistics, Computer Science, or Mathematics with at least 7+ years of relevant experience is required ; OR Master’s Degree in Statistics/Biostatistics, Computer Science, or Mathematics with at least 5+ years of relevant experience is required.
  • 5+ years of experience as a statistical programmer in the pharmaceutical industry is preferred.
  • Demonstrated knowledge and ability in efficient programming techniques
  • Working knowledge of clinical research, Good Clinical Practices, and regulatory requirements/guidelines.
  • Technically strong with regard to statistical programming processes and activities.
  • Highly proficient in SAS.
  • Experience as a lead statistical programmer on several concurrent projects.
  • Understanding of CDISC STDM/ADaM guidelines.
  • Excellent English verbal and written communication skills; good organizational and interpersonal skills.
Benefits
  • Medical, Dental and Vision Plan Options
  • Health and Financial Wellness Programs
  • Employer Assistance Program (EAP)
  • Company Paid and Voluntary Life/AD&D, Short-Term and Long-Term Disability
  • Healthcare and Dependent Care Flexible Spending Accounts
  • 401(k) Retirement Plan with Company Match
  • 529 Education Savings Program
  • Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks
  • Paid Time Off (PTO) includes: 11 Holidays
  • Exempt Employees are eligible for Unlimited PTO
  • Non-Exempt Employees are eligible for 10 Vacation Days, 56 Hours of Health Pay, 2 Personal Days and 1 Cultural Day
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
statistical programmingSASdata standardizationprogramming macrosstatistical analysis plansanalysis datasets specificationsclinical trial data submissionprogramming techniquesdata presentationsedit checks
Soft Skills
communication skillsorganizational skillsinterpersonal skillsmentoringguidanceinfluencesupportproblem-solvingleadershiptraining