Biostatistician

Penfield Search Partners; West Yorkshire; On-site; GBP 50,000 - 70,000; Full time

Job summary

A statistical consulting firm in the United Kingdom is seeking an experienced statistical professional to provide support for observational studies and clinical trials. The role requires a PhD or MS in Biostatistics or Statistics and a minimum of 4 years of relevant experience in the pharmaceutical industry. The successful candidate will author statistical analysis plans and conduct analysis for Real World Evidence studies. This contract position requires UK-based candidates only.

Qualifications

• 4+ years experience in pharmaceutical industry providing statistical input into study design.
• 4+ years with Phase-4 studies and Medical Affairs.
• 4+ years experience using SDTM and ADaM data standards.

Responsibilities

• Support statistical protocol development for studies.
• Author and review statistical analysis plans and dataset specifications.
• Conduct analysis for Medical Affairs Real World Evidence studies.

Skills

Statistical analysis

Programming in SAS

Programming in R

Real World Evidence methodologies

Advanced statistical models

Education

PhD or MS in Biostatistics or Statistics

Tools

SAS

R

Job description

Job Description

Contact: Neisha Camacho / Terra Parsons -

No 3rd party candidates

Candidates must be UK based

Key Responsibilities

• Provide statistical support in protocol development for observational studies and / or clinical trials.
• Author and review of statistical analysis plans analysis dataset specifications and TFL shells.
• Work with programming and other cross-functional teams in Phase-4 non-interventional study to develop CRF validate and review the datasets and results.
• Conduct programming and analysis for Medical Affairs RWE studies.
• Support develop abstract poster and manuscript as deliverables.

Education & Qualifications

• Education : PhD or MS in Biostatistics or Statistics
• Experience in pharmaceutical industry to provide statistical input into the study design statistical analysis and reporting of interventional and observational studies.
• Min 4 yrs experience with Phase-4 study Medical Affairs study Real World Evience (RWE) or HEOR study.
• Min 4 yrs experience in statistical software SAS and R.
• Min 4 yrs experience with SDTM and ADaM data standards.
• Min 4 yrs experience with Real World Data (RWD) and RWE methodologies such as propensity score analysis causal inference.
• Min 4 yrs experience with advanced statistical models such as mixed effect model approaches for repeated measures Machine Learning (ML) methods.

Employment Type: Contract

Experience: years

Vacancy: 1