Lead Statistical Programmer

3 weeks ago

London, Greater London, United Kingdom IQVIA Full time

IQVIA is seeking experienced statistical programmers proficient in the SAS programming language to create clinical study report documentation in alignment with clinical trial objectives for regulatory submissions. This role encompasses a wide range of statistical programming tasks within our DS3 environment (remote):

Key Responsibilities:

  • Extract and integrate data from diverse sources
  • Develop quality control procedures for source data and address reporting discrepancies
  • Analyze project-level requirements and formulate programming specifications
  • Craft programming code adhering to established Good Programming Practices
  • Generate ADaM datasets
  • Create statistical analysis tables, listings, and figures
  • Validate datasets and all statistical outputs according to defined gate checks
  • Collaborate with internal and client statisticians and clinical team members to ensure clarity of requirements and timelines
  • Advocate for the use of established standards, SOPs, and best practices
  • Export data and clinical study report documentation
  • Mentor and train team members and departmental staff

Contribute to the advancement of clinical trial statistical analysis in a forward-thinking environment. Recognized for innovation, we provide access to state-of-the-art in-house technology, enabling you to engage in global projects across various therapeutic areas. Experience a dynamic team atmosphere that fosters collaboration in conducting biostatistical analyses and sophisticated statistical programming. Opportunities for professional development and mentorship at all levels empower you to shape your long-term career path.

Candidate Profile:

We understand that impactful results require not only the right methodology but also the right talent. Ideal candidates should hold a Master's or Bachelor's degree in Biostatistics, Statistics, Mathematics, or Computer Science, with substantial educational or practical experience in programming.

Essential Skills:

  • Remote Work Capability
  • Over 5 years of experience in a Statistical Programmer role within CRO/Pharma, specifically with ADaM and TFL
  • Exceptional accuracy, attention to detail, problem-solving, organizational, and interpersonal communication skills
  • Proficiency in SAS programming within the CRO/Pharma/Biotech/Healthcare sectors
  • Strong knowledge of statistics and the ability to perform routine and complex analytical tasks
  • Commitment to quality, accuracy, and thoroughness in work activities
  • Excellent communication abilities
  • Familiarity with Good Clinical Practice and ICH guidelines
  • Capability to independently lead projects, estimate programming scope, manage resource assignments, communicate work status, and adhere to project timelines
  • Initiative and reliability in completing tasks with integrity
  • Self-awareness to recognize when negotiation skills and assistance are required
  • Ability to establish and maintain effective working relationships with colleagues, managers, and clients

Embrace your curiosity and advance your career in an engaging environment where professional growth is prioritized. Challenge conventional thinking and enjoy your work. Discover a career with a greater purpose and contribute to creating a healthier world.

At IQVIA, we are a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We are committed to pushing the boundaries of human science and data science to maximize our impact, helping our clients create a healthier world.

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