Contract Biostatistician - 6 months
As Statistician the successful candidate will be responsible for the following duties:
- Responsible for all statistical tasks on the assigned clinical trials: clinical trial design/planning, analysis plan, reporting activities including exploratory analyses, and additional analysis to support publications
- Providing statistical consultation to clinical team and support decision making process by providing adequate information
- Tracking clinical trial/allocated project activities and milestones
- Ensuring timeliness and adequate quality of all Biostatistics and Statistical Reporting (B&SR) deliverables for the assigned trials
- Following processes and adhere to company and project specific standards as well as Health Authority requirements (SOPs, Master Analysis Plan, GCP, and regulatory guidelines)
- Participating in or leading non-clinical project activities as needed
- Application and extension of existing Bayesian methods for dose finding and proof of concept
- Establishing and maintaining sound working relationships and effective communication within the Clinical Trial Team and B&SR team
As Statistician, you will have the following qualifications, skills and experience:
- Masters Degree in Statistics (or equivalent degree) with experience or PhD in Statistics (no previous experience is required)
- Knowledge and expertise in Statistics, in particular the use of applied Bayesian statistics in decision making
- Knowledge of statistical software packages (e.g. WinBUGS, R, SAS)