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Data Analyst
2 months ago
In this role we are looking for individuals with a quantitative science background (statistics, data science, computer science, mathematics, or similar), database and programming expertise, and a passion for drug development. The candidate for this role will primarily work within the Biomedical Data Stewardship team, but may also collaborate with an analytic group within Global Statistical Science team here at company. This role will have an opportunity to work across client's pipeline to participate in and lead the extraction, consolidation, analysis, and presentation of complex internal and external clinical trial data standards.
Responsibilities:
- Build a comprehensive understanding of Client's data standards structure across stages of development
- Build a comprehensive understanding of the Metadata Repository (MDR) product and design, and identify areas for improvement and expansion
- Develop integrations with the MDR enabling visualization of the standards, compliance reporting, and metrics
- Use SAS Enterprise Guide to develop and maintain SAS programs to extract Data Element Standards and to create datasets, reports, and workbooks
- Develop and maintain VBA programs to post-process SAS output and automate repetitive document/file processing activities
- Support development of machine learning and other statistical model
Top 3 Must Have Skill Sets:
- Excellent R computing, SAS, modeling, and visualization skills
- Experience working with multiple languages in the Shiny environment (for example. JavaScript, CSS, Python, VBA, etc.)
- Independent and self-motivated / Strong organizational skills / Strong communication and collaboration skills
Basic Qualifications:
- Master's degree and 3 years quantitative science experience OR Bachelor's degree and 5 years quantitative science experience OR Proficient in SAS programming language
- Good understanding of clinical trials and clinical data
- Proficient in R programming language and Shiny app development
Preferred Qualifications:
- Doctoral degree or master's degree with relevant experience
- 4 or more years of pharmaceutical/biotech experience in drug development
- Proven project leadership experience
- Experience in designing, analyzing, and reporting clinical trials
- Excellent SAS and/or R computing, modeling, and visualization skills
Compensation:
The pay rate range above is the base hourly pay range that Aditi Consulting reasonably expects to pay someone for this position (compensation may vary outside of this range depending on several factors, including but not limited to, a candidate's qualifications, skills, competencies, competencies, competencies, experience, location and end client requirements).
Benefits and Ancillaries:
Medical, dental, vision, PTO benefits and ancillaries may be available for eligible Aditi Consulting employees and vary based on the plan options selected by the employee.
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