Bio Statistician - Clinical Research - Pharma/Healthcare

- 4+ years of experience as a statistician and/or statistical programmer with at least 2+ years direct experience using observational/real-world data (RWD) in the pharmaceutical or medical device sector.

- Demonstrated experience of leading analyses for RWE studies to meet regulatory requirements within the agreed upon budget, timeline, and resources.

- Experience with advanced statistical methods utilized for RWE studies (e.g., propensity score matching) and eagerness to continuously learn and expand statistical expertise.

- Expert in SAS programming.

- Experience using the Premier Healthcare Database is required.

- Experience with large healthcare databases (e.g., Truven MarketScan, Optum Clinformatics) and other data models (e.g., OMOP, CDM).

- Familiarity with relevant medical coding vocabularies (e.g., ICD, CPT, HCPCS, LOINC)

- Certification in Research HIPAA, Good Clinical Practice, Human Subject Protection, Healthcare Quality Principles preferred.