
Senior Data Scientist for Clinical Trials
2 weeks ago
This role involves providing statistical support to projects within the Vaccines area.
The successful candidate will collaborate with project teams and provide expertise in designing research concepts, developing protocols, writing statistical analysis plans, performing analyses, interpreting results, and presenting findings.
Responsibilities include providing scientific input on post-hoc / ad-hoc analysis requests, developing statistical analysis plans, and leading multiple project teams by applying project management skills and statistical techniques.
The ideal candidate will have a strong understanding of ICH guidelines and clinical trial design as applicable to statistics, effective communication skills, and experience with statistical modelling of clinical data and programming languages such as R or SAS.
Qualifications:
- Masters in Statistics/Biostatistics (or related field) with 8+ years' experience in clinical trials, or PhD in Statistics/Biostatistics (or related field) with 4+ years' experience in clinical trials.
- Effective verbal and written communication skills.
- Understanding of broad statistical theory and its application.
- Able to fully understand clinical questions and concepts and translate them into SAP development followed by data generation all the way through publication.
- Experience with statistical modelling of clinical data and statistical inference.
- Experience in R or SAS programming languages.
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