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IQVIA

Runs drug trials and sells health data to pharma

Senior Statistical Programmer in Pharmacometrics - Multiple Teams

Quantitative Biology & BiostatisticsConfirmed live in the last 24 hours
Full-timeNo salary listed

About the Job

Requirements

  • A bachelor's degree in Statistics, Computer Science, or a related field.
  • At least 2 years working with efficacy analysis (ADaM datasets and TLFs) and/or at least 4 years in ADaM statistical programming on clinical trials.
  • Hands-on proficiency in the R programming language is mandatory.
  • Proficiency in the SAS programming language.
  • Advanced English proficiency in both written and spoken communication; this is tested during the interview process.
  • A native LATAM language: Spanish or Portuguese.
  • Ability to lead and manage others, ensuring adherence to standards and mentoring junior programmers.
  • Ability to maintain confidential information, sensitive project data, and internal communications.
  • Sound judgment and decision-making when selecting statistical methods and programming techniques.
  • Ability to manage time and resources to deliver high-quality programming outputs within tight deadlines.
  • Project management skills to coordinate tasks and resources efficiently.
  • Technical aptitude and deep understanding of SAS programming and CDISC standards.
  • Ability to analyze and interpret financial data accurately for informed decision-making in statistical programming.
  • Problem-solving skills to overcome programming challenges and optimize workflows.
  • Written and verbal communication skills to document programming methodologies and procedures clearly and facilitate collaboration and process improvement with cross-functional teams.
  • Ability to inspire and motivate programming teams to align their work with organizational goals and quality standards.

Responsibilities

  • Develop and validate complex datasets and outputs using SAS programming, ensuring compliance with CDISC standards, including ADaM and SDTM models.
  • Collaborate with cross-functional teams to optimize statistical programming processes and improve efficiency and accuracy.
  • Provide technical guidance on statistical methodologies to support clinical trial projects and departments.
  • Mentor and guide junior programmers.
  • Contribute to continuous improvement of programming workflows and departmental standards.
  • Ensure high-quality deliverables from the statistical programming department by following best practices and established protocols.
  • Lead initiatives to enhance programming tools and techniques.
  • Partner with leadership to align programming objectives with organizational goals.

About the Company

IQVIA

Runs drug trials and sells health data to pharma

IQVIA runs clinical trials for drug, biotech and medical device companies and sells them the health data, software and analytics they use to develop and market treatments. Its research arm designs studies, recruits trial sites and patients, and manages trials through to regulatory filing. Its commercial arm sells market data, consulting and software that pharma sales and marketing teams use to plan product launches. Clients pay through multi-year service contracts and data and software subscriptions. IQVIA was formed in 2016 when clinical research firm Quintiles merged with health data company IMS Health, and it is based in Durham, North Carolina.

Company size
10,001+
Company stage
IPO
Headquarters
Durham, NC
Founded
1998

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