The Associate Director provides Statistical Programming leadership and expertise in support of clinical development and post‐marketing activities for multiple therapeutic areas. Participates in the development, registration, and life cycle management of Grifols products.

Drives standardization within the Biometry group, innovating to develop processes/systems/tools designed to improve automation and efficiency of all aspects of reporting of clinical trials – including standard checking of deliverables generated by Contract Research Organizations (CROs).

Contributes strategically to project decisions with a focus on pre-study planning, reporting and submission preparation within and across projects.

What you'll do 

The duties and responsibilities include, but are not limited to, the following: