Biostatistician
đź“Ť Location: London, UK (Remote)
🕒 Duration: 1–2 Years Contract
We are seeking a highly skilled Biostatistician with strong experience in Real World Evidence (RWE), Medical Affairs, and Phase 4 studies to join our team. The ideal candidate will provide statistical expertise across study design, analysis, and reporting within interventional and observational research.
Key Responsibilities:
* Provide statistical input in the design, analysis, and reporting of observational and/or clinical studies.
* Author and review statistical analysis plans (SAPs), analysis dataset specifications, and TFL shells.
* Collaborate with programming and cross-functional teams to develop CRFs, validate datasets, and review results for non-interventional Phase 4 studies.
* Conduct programming and analysis for Medical Affairs and RWE projects.
* Contribute to the development of abstracts, posters, and manuscripts for publication.
Core Skills & Experience:
* PhD or Master’s degree in Biostatistics or Statistics.
* Minimum 4 years’ experience in the pharmaceutical industry providing statistical input for interventional or observational studies.
* Proven experience with Phase 4, Medical Affairs, RWE or HEOR studies.
* Proficiency in SAS and R (minimum 4 years).
* Hands-on experience with SDTM and ADaM data standards.
* Strong knowledge of Real World Data (RWD) and RWE methodologies, including propensity score analysis and causal inference.
* Experience with advanced statistical modeling, including mixed-effects models and Machine Learning (ML) approaches.
Why Join Us:
* Opportunity to contribute to impactful research in Real World Evidence and Medical Affairs.
* Work remotely with a collaborative, global team.
* Long-term project stability (1–2 years).