Senior Statistical Analyst - RWE - SAS programming

410 ICR United States USA
Wilmington, NC, United States
3 days ago
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Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Experience level
Expert
Experience required
5 years minimum
Working hours
Regular working hours

Tech stack

Clinical Data Management Computer Programming Python (Programming Language) SAS (Software) Extensible Markup Language (XML) Information Technology Data Management

Job description

  • Develop and validate analysis datasets, tables, listings and figures.
  • Apply programming standards and specifications consistently.
  • Perform quality control and resolve data or programming issues.
  • Collaborate with biostatistics, data management and clinical stakeholders.
  • Maintain traceable programming documentation and submission readiness.
  • Provide technical guidance, peer review or mentoring on complex work within the discipline.

Requirements

  • Degree in statistics, mathematics, computer science or related quantitative discipline, or equivalent relevant programming expertise.
  • Minimum of 5 years of experience in statistical analysis within the pharmaceutical, biotechnology, or CRO industry.
  • Proficiency in statistical software SAS (R or Python are also used in a more limited capacity)
  • Understanding of clinical trial design, statistical methodologies, and regulatory requirements.
  • Practical statistical programming experience in clinical trials using SAS or another appropriate statistical programming environment.
  • Knowledge of CDISC SDTM and ADaM standards.
  • Understanding of clinical trial data, statistical outputs and validation practices.
  • Experience developing and validating analysis datasets, tables, listings and figures.
  • Experience reviewing colleagues’ work and providing technical guidance on clinical statistical programming., * Experience supporting regulatory submissions.
  • SAS programming capability (R or Python are also used in a more limited capacity)
  • Advanced CDISC or Define XML expertise.

Benefits & conditions

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

About the company

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

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