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.You will be joining highly experienced industry leader, working directly with the head of Biometrics, who will be available to offer direct support and training in this role in a shared learning team environment.Working in a smaller company and team setting. You will be taking a strategic and managerial lead on the programming initiatives, where you will be fully involved in creating/adapting business strategy as well as development of junior programmes on the team - 50/50.This role would suit an experienced Principal Statistical Programmer with extensive CDISC and clinical trial knowledge, strong strategic mindset, and ability to lead sponsor meetings.Responsibilities:Working 100% remote, you will be responsible for:
- Lead programming initiatives and present in internal/external meetings.
- Manage small programming team.
- Using 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.
- BSc in a scientific or related field.
- At least 5 years' experience statistical programming within the pharmaceutical industry.
- Clinical Trial experience (Phases I-III)
- CDISC experience (ADaM and SDTM datasets)
- Title: Principal Statistical Programmer
- Location: Remote Australia
- Salary: $130,000 - $155,000 plus superannuation (open to negotiation)