Biostatistician

Clinical/Medical Research (Healthcare & Medical)

Opportunity for an experienced Statistical Programmer to join an independent CRO.
You will be a part of a small biometrics team responsible for leading multiple studies in oncology, cardiology, and respiratory therapeutic areas - through phases I-III.
Although smaller in size, the team operates on a global scale and so will see you working in a close team setting but having access to global studies.
You will be working alongside experienced industry leaders, who will be available to offer direct support and training in this role and so is a good opportunity for anyone looking to upskill.
This role would suit an experienced statistical programmer who has experience working on clinical trials.
Responsibilities: Working 100% remote, you will be responsible for: Programme in SAS to create tables, listings, and figures from project specifications.
Lead communications with sponsors in accordance with statistical programming queries.
Design and develop compliant programmes for study teams.
Review of statistical analysis plans and mock outputs.
Lead programme initiatives for multiple clinical trials across phases I-III.

Skills:

BSc in a scientific or related field.
At least 2 years' experience statistical programming within the pharmaceutical industry.
Clinical Trial experience (Phases I-III) CDISC experience (ADaM and SDTM datasets)

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