
Senior Statistical Programmer
ImmunityBio, Inc.
full-time
Posted on:
Location Type: Remote
Location: California • United 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