Principal Biostatistician Consultant - Remote (experience working with medical affairs and commercial)

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds….

ClinChoice is searching for an Principal Biostatistician Consultant to join one of our clients.

ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.

Position Description:

We are seeking an experienced Contract Biostatistician to support Medical Affairs and Real‑World Evidence (RWE) activities. The role will provide statistical leadership in the design, analysis, and interpretation of RWE/observational studies, external comparator analyses, and evidence generation strategies to support post‑marketing, payer, and hypothesis generation analysis. This position requires close collaboration with cross-functional teams including Medical, HEOR, Clinical Development, and Commercial.

Responsibilities and Duties

• • Partner with medical for publication strategies, HEOR or economic modeling inputs

• • Provide statistical expertise in analyses using external control and/or synthetic control, meta-analyses, and causal inference analyses, e.g. propensity score matching method

• • Contribute to manuscripts, abstracts and presentations

• • Collaborate with HEOR to align analyses with HTA agency expectations

• • Review protocols for real world evidence studies

• • Work with statistical programmers to conduct ad hoc analyses; Conduct quality review of statistical analyses

• • Perform statistical programming for advanced statistical methodologies and help statistical programmers QC their programs

• • Review relevant medical literature

• • Write statistical analysis plans

• • Develop TLF shells and review programming specs

• Minimum Requirements:

• Experience:

• • M.S., Biostatistics or Ph.D. in Biostatistics or equivalent with at least 5 years of pharmaceutical, biotechnology, or equivalent experience.

• Other:

• • Prior experience working with medical affairs and commercial

• • Good understanding of meta-analyses and causal inference methodologies

• • Familiarity with regulatory guidance on RWE and HTA requirements

• • Strong statistical reasoning and problem-solving

• • Ability to communicate complex methods to non-statistical stakeholders

• • High attention to data quality and methodological rigor

• • Ability to work independently in a fast-paced, cross-functional environment

• • Understand good clinical practice guidelines

• • Good statistical programming skills using relevant statistical software

• • Oncology experience preferred

• #LI-TT1 #LI-Remote #Principal#Contract