Senior RWE Data Programmer & Analyst

Cytel; Raleigh (NC); On-site; USD 110,000 - 160,000; Full time

Job summary

Cytel is seeking an experienced professional to support the Epidemiology team with Real World Data (RWD) analytics. You will program and conduct statistical analyses, code data, create algorithms, and link datasets to enable observational studies.

Collaborating with epidemiologists, you will manage stakeholder relationships, prioritize multiple projects, and deliver timely results. You will present findings and contribute to study reports and regulatory documents as needed.

Qualifications

• Master’s or PhD in a related field and 5+ years of RWE analytics experience.
• Proficiency in SQL is required; SAS or R proficiency is also required.
• Experience with RWE data sources such as Optum, Truveta, UK Biobank is highly valued.

Responsibilities

• Provide support to Epidemiology by preparing Real World data and advising on analytic strategies.
• Program and conduct statistical analyses including data coding, algorithm creation, and dataset linkage.
• Support medical affairs and regulatory activities with observational data analyses.
• Partner with epidemiologists to manage stakeholder relationships and deliver timely results.
• Produce tables/figures for study discussions and reports and present results to clients.

Skills

SQL proficiency

SAS or R

RWE analytics

Relational databases

Applied statistics

Project management

Communication skills

Education

Master’s or PhD in epidemiology, biostatistics, statistics, bioinformatics, economics

Tools

Optum Clinformatics Datamart

Market Clarity

Truveta

UK Biobank

Job description

Cytel is seeking an experienced professional to support the Epidemiology team with Real World Data (RWD) analytics. You will program and conduct statistical analyses, code data, create algorithms, and link datasets to enable observational studies.

Collaborating with epidemiologists, you will manage stakeholder relationships, prioritize multiple projects, and deliver timely results. You will present findings and contribute to study reports and regulatory documents as needed.