Biostatistician I conducts statistical studies to generate data and insights used to innovate, plan and support improved healthcare outcomes and processes. Prepares analysis plans to ensure the best statistical methods are developed and utilized. Being a Biostatistician I writes specifications for files, consistency checks, tables, and calculations used to collect and analyzes data from a variety of sources. Interprets analyses and prepares exhibits for reports and presentations. Additionally, Biostatistician I interfaces with non technical users to assist with data interpretation and understanding of results. Proficient with statistical computer applications like SAS and R. Requires a master’s degree of biostatistics, statistics, mathematics or related field. Typically reports to a supervisor or manager. The Biostatistician I work is closely managed. Works on projects/matters of limited complexity in a support role. To be a Biostatistician I typically requires 0-2 years of related experience.
Biostatistician Job Description Template
Our company is looking for a Biostatistician to join our team.
Responsibilities:
- Review literature for new statistical methods and techniques;
- Reviews statements of work and writes the statistical analysis sections to ensure sufficient power is obtained with the study design;
- Generate statistical outputs such as tables, listings and figures to support the clinical study report;
- Provides leadership and work guidance to less experienced personnel;
- Assist in the development of quality control procedures for data analysis;
- Develops rules, benchmarks, etc. for the analysis and interpretation of model data;
- Clearly communicates the rationale for analyses and the outcomes to internal team and client, orally and in writing;
- Supports multiple functional areas, including manufacturing, nonclinical and clinical research;
- Prioritize and manage workload on multiple project requests within deadlines;
- Contribute to clinical development plan preparation;
- Assist with development and implementation of teaching materials and educational seminars;
- Reviews work performed by statistical subcontractors;
- Development of detailed Data Analysis Plan for assigned projects;
- Study design for clinical and translational research efforts;
- Develop Statistical Analysis Plans (SAP) and compute sample sizes.
Requirements:
- Candidate should have a proven ability to understand biomedical literature/terminology;
- Occupational Health Survey;
- Experience using R for biostatistical analysis required;
- Minimum Education: Master’s degree in epidemiology, statistics, or related life sciences field;
- Master’s degree in statistics or mathematics, with a PhD in statistics or mathematics preferred;
- Experience working with statistical, data-collection and test development procedures;
- Strong communication skills for gathering and presenting test results to individuals and groups;
- Experience working with metrics tools and processes;
- Leadership skills to guide and mentor the work of less experienced personnel;
- Personal computer and industry standard statistical analysis tools skills;
- Strong analytical and problem-solving skills;
- Previous experience in a pharmaceutical or CRO setting desirable;
- Experience working with company used databases, statistical software packages and operating systems;
- Knowledge of regulatory requirements/guidelines for drug development; and;
- Must have excellent written and verbal communication skills.