Senior Biostatistician

ProPharma; United Kingdom; On-site; GBP 50,000 - 70,000; Full time

Job summary

A leading company in the pharmaceutical industry is seeking a Senior Biostatistician to design and execute statistical analyses for clinical trials. The role requires expertise in statistical methodologies, excellent communication skills, and proficiency in SAS or R. The candidate will collaborate with cross-functional teams to ensure the quality of statistical deliverables and mentor junior statisticians.

Qualifications

• 3+ years of relevant work experience in biostatistics.
• In-depth knowledge of statistical methodologies.

Responsibilities

• Lead statistical activities for clinical trials and data analyses.
• Ensure quality and accuracy of statistical deliverables.

Skills

Communication

Project Management

Statistical Methodologies

Education

Ph.D. in Biostatistics

M.S. in Biostatistics

Tools

SAS

R

Job description

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The Senior Biostatistician position is responsible for designing and executing statistical analyses, providing statistical expertise to cross functional teams, and ensuring the quality and accuracy of statistical deliverables.

Essential Functions:

• Lead statistical activities for clinical trials and data analyses, including study design, statistical analysis plan development, and statistical analysis.
• Provide statistical expertise to cross functional teams, including clinical operations, data management, and regulatory affairs.
• Ensure the quality and accuracy of statistical deliverables, including statistical reports, tables, listings, and graphs.
• Participate in the development and review of clinical study protocols and case report forms (CRFs) to ensure appropriate statistical analysis.
• Develop and maintain SAS programs for statistical analysis in accordance with standard operating procedures (SOPs), good programming practices, and regulatory guidelines.
• Keep up to date with regulatory guidelines and industry standards related to biostatistics and ensure compliance with these guidelines.
• Participate in the development and maintenance of internal processes and standard operating procedures to improve statistical efficiency and consistency.
• Provide guidance and mentorship to junior statisticians.
• Other duties as assigned.

Necessary Skills and Abilities:

• In-depth knowledge of statistical methodologies.
• Excellent communication and interpersonal skills, with the ability to work collaboratively in cross functional teams and with external partners.
• Strong project management skills, with the ability to manage multiple projects simultaneously.
• Knowledge of regulatory requirements and guidelines related to statistical analysis and reporting of clinical trial data.
• Ability to program in SAS and or R.

Educational Requirements:

• Ph.D. in Biostatistics, or M.S. in Biostatistics.

Experience Requirements:

• 3+ years of relevant work experience.
• Outsourcing industry experience required.
• Experience in clinical trial design, sample size calculations, and statistical analysis.
• Experience with CDISC data structures, such as SDTM and ADaM.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Health Care Provider, Science, and Research

• Industries

  Business Consulting and Services, Biotechnology Research, and Research Services

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