Principal Statistical Programmer, RWE

IQVIA Argentina; Durham (NC); Remote; USD 60,000 - 80,000; Full time

Job summary

An innovative firm is seeking a Principal Statistical Programmer to join their RWE biometrics team. In this role, you will work closely with study statisticians to design data structures and ensure compliance with CDISC standards. Your expertise in SAS and R programming will be essential as you lead programming efforts for health outcomes and epidemiology studies. This position offers an opportunity to leverage real-world data and contribute to significant study initiatives. If you have a strong background in statistical programming and a passion for clinical research, this is the perfect opportunity to advance your career while working from the comfort of your home.

Qualifications

• 7+ years of experience in pharmaceutical or clinical research settings.
• Strong knowledge of CDISC standards and SAS programming.

Responsibilities

• Collaborate with statisticians to design data structures for study deliverables.
• Ensure programming activities comply with CDISC standards.

Skills

SAS Programming

R Programming

Data Analysis

Organizational Skills

Communication Skills

Education

Bachelor's degree in Statistics

Bachelor's degree in Mathematics

Bachelor's degree in Computer Sciences

Bachelor's degree in Pharmacology

Bachelor's degree in Biology

Tools

CDISC Standards

ADaM Datasets

Job description

Summary: IQVIA is hiring a Principal Statistical Programmer to join a sponsor-dedicated, RWE biometrics team. Expect to work fully within the sponsor environment to progress with long-term study initiatives. Contribute to establishing processes and standards for RWE/RWD and establish yourself as a key resource in this area. Apply your skills in both SAS and R programming.

Job Expectations:

• Serves as statistical programming member and represents Biometrics on health outcomes and epidemiology studies.
• Collaborates with the study statistician to design data structure and specifications for programming study deliverables including ADaM datasets, Tables, Listings and Figures. Contribute to leading the production and validation efforts for the outputs.
• Ensure all programming activities comply with CDISC standards (SDTM and ADaM) and regulatory guidelines.
• Leverages administrative claims, electronic medical records, or other real-world data to complete appropriate study tasks.
• Identifies innovation opportunities for the use of real-world data (RWD).

Qualifications:

• Bachelors degree in Statistics, Mathematics, Computer Sciences, Pharmacology, Biology or similar.
• Ideal candidates will have 7+ years of experience working within a pharmaceutical or clinical research setting.
• Must have excellent knowledge of CDISC standards.
• Strong SAS programming skills when applying to clinical trial data.
• Moderate level skills in R programming with organizational and data analysis purposes.
• Experienced with handling real-world data (RWD) with advanced content knowledge.
• Experienced with clinical trial data and extremely hands-on in data manipulations, analysis, and reporting of analysis results.
• Excellent organizational skills and proven ability to effectively lead multiple projects to successful completion.
• Ability to effectively interpret and communicate research results to internal and external audiences.

Location: Work-from-home. Candidates located in the U.S. or Canada can be considered.