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 materials aligned with the objectives of clinical trials for regulatory submissions. This role encompasses a wide range of statistical programming tasks within our DS3 environment (home based):

Key Responsibilities:

  • Import data from diverse sources
  • Develop quality control checks for source data and address reporting data issues
  • Analyze project-level requirements and formulate programming specifications
  • Write programming code adhering to established Good Programming Practices
  • Create ADaM datasets
  • Generate statistical analysis tables, listings, and figures
  • Validate datasets and all statistical outputs according to prescribed gate checks
  • Collaborate with internal and client statisticians and clinical team members to ensure a clear understanding of requirements and timelines
  • Advocate for the use of established standards, SOPs, and best practices
  • Export data and clinical study report materials
  • Provide training and mentorship to team members and departmental staff

You can contribute to advancing clinical trial statistical analysis. Recognized for innovation, we offer access to cutting-edge in-house technology, enabling you to engage in global projects across various therapeutic areas. Experience a dynamic team environment that fosters collaboration in biostatistical analyses and advanced statistical programming. Opportunities for development and mentorship at all levels support your long-term career progression in your chosen direction.

Candidate Profile:

We understand that achieving meaningful results requires not only the right approach but also the right individuals. Candidates should hold a Master's or Bachelor's degree in Biostatistics, Statistics, Mathematics, or Computer Science, with strong educational or practical experience in programming.

Essential Skills:

  • Home Based/Remote
  • 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
  • Experience in SAS programming within the CRO/Pharma/Biotech/Healthcare sectors
  • Knowledge of statistics with routine and occasionally complex analytical skills
  • Commitment to quality, accuracy, and completeness in work activities
  • Strong communication abilities
  • Understanding of Good Clinical Practice and ICH guidelines
  • Capacity to independently lead or demonstrate lead potential, estimate programming scope of work, manage resource assignments, communicate work status, and adhere to project timelines for deliverables
  • 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 exciting environment where development is prioritized. Think innovatively and challenge conventional thinking. Enjoy your work and discover a career with greater purpose, contributing to a healthier world.

Whatever your career aspirations, we are dedicated to supporting your journey.

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to create the most significant impact possible – assisting our customers in fostering a healthier world.

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