As a Statistician, you are responsible for providing statistical support for clinical trials. You will design clinical trial protocols, write statistical analysis plans, and conduct statistical analyses.
PROFIEL VAN DE GESCHIKTE INTERIM PROFESSIONAL:You have good communication and organisational skills, and experience in running RCT's within pharma or similar industries.
Who are you?
- PhD in Statistics, Biostatistics, or equivalent;
- 4 years of experience in clinical trial design and analysis;
- Strong and broad knowledge of statistical methods for clinical trials, including experience with survival analysis, mixed models, and non-parametric methods;
- Experience with software packages such as SAS and R;
- Knowledge of regulatory requirements for clinical trials, including FDA, EMA, and ICH guidelines;
- Excellent communication and interpersonal skills, with the ability to work effectively in a team-oriented environment;
- Strong problem-solving skills and attention to detail.