Associate Director, Biostatistics
Location: Virginia
Company: Leading Pharma
Qualifications:
- Education: PhD in Biostatistics, Statistics, or a related field.
- Industry Experience: CRO and/or Sponsor-Side Experience
- Programming Skills: SAS (Hands-on abilities)
- Strong CRO / Vendor oversight experience
Responsibilities:
- Provide expert statistical guidance for clinical trial design, analysis, and interpretation.
- Prepare and review statistical sections of regulatory submissions, including INDs, NDAs, and other regulatory documents.
- Oversee statistical analysis plans, data interpretation, and reporting for multiple clinical trials.
- Ensure timely and accurate delivery of statistical results by working closely with CRO team.
- Provide mentorship and guidance to junior level team members.