Responsible for executing Biostatistics strategy through collaboration on clinical study documents, oversight of vendors, and innovative statistical methodology in a biotech environment.

The Associate Director, Analytical Sciences will oversee analytical development at contract labs, ensuring method validation and compliance with regulatory standards while managing vendor relationships and analytical strategies.

The Director, CQA/GCP Auditing Lead oversees GCP audits, ensuring compliance across clinical studies. Responsibilities include planning audits, writing reports, tracking metrics, and supporting inspection readiness.

The Senior Manager, Statistical Programming oversees statistical programming for clinical trials, ensuring accuracy in analyses and outputs, and collaborates with CROs. They handle SAS programming, develop statistical outputs, and participate in study teams and reporting.