Biostatistician
Biostatistician
Medpace
Lyon, France
Responsibilities
- Contribute to clinical development of plan preparation;
- Review of study protocol and preparation of statistical methodologies;
- Programming of study analysis, review of study results and preparation of statistical methods section for clinical/statistical reports;
- Communicate project requirements for CRF design, database design and database cleanup to ensure the key study variables are suitable for analysis; and
- Communicate statistical results to medical writing personnel to ensure accurate interpretation.
Qualifications
- Ph.D. degree in Biostatistics/Statistics with strong experience in SAS Programming or equivalent; and
- 1-2 years of experience in a pharmaceutical or CRO setting preferred.
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