Freelance Biostatistician
Posted 4 days ago by Walker Cole International
Negotiable
Undetermined
Undetermined
England, United Kingdom
Summary: The role of Freelance Biostatistician involves providing statistical expertise for clinical trial design, analysis, and reporting within a pharmaceutical company. The position requires collaboration with cross-functional teams and adherence to regulatory standards. Candidates should have proven experience in biostatistics, particularly in pharma or CRO settings, and be proficient in SAS or R. A relevant MSc or PhD is also required for this contract-based position.
Key Responsibilities:
- Provide statistical expertise across clinical trial design, analysis, and reporting.
- Develop and review Statistical Analysis Plans (SAPs).
- Conduct statistical analyses using SAS or R.
- Interpret and communicate findings to internal and external stakeholders.
- Ensure compliance with MHRA, EMA, and FDA regulatory standards.
Key Skills:
- Proven experience as a Biostatistician in pharma or CRO settings.
- Strong knowledge of clinical trial methodology and regulatory frameworks.
- Proficiency in SAS and/or R.
- MSc or PhD in Biostatistics, Statistics, or a related field.
- UK-based and eligible to work as a contractor.
Salary (Rate): undetermined
City: undetermined
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
We’re working with a pharmaceutical company seeking an experienced Biostatistician to join their team on a contract basis. This is a fantastic opportunity to contribute to impactful clinical development programs and collaborate with cross-functional teams in a dynamic, science-driven environment.
Job Requirements:
- Provide statistical expertise across clinical trial design, analysis, and reporting.
- Develop and review Statistical Analysis Plans (SAPs).
- Conduct statistical analyses using SAS or R.
- Interpret and communicate findings to internal and external stakeholders.
- Ensure compliance with MHRA, EMA, and FDA regulatory standards.
Experience needed:
- Proven experience as a Biostatistician in pharma or CRO settings.
- Strong knowledge of clinical trial methodology and regulatory frameworks.
- Proficiency in SAS and/or R.
- MSc or PhD in Biostatistics, Statistics, or a related field.
- UK-based and eligible to work as a contractor.