Lead impactful biostatistical strategies for clinical development phases I-IV. Collaborate with cross-functional teams to optimize trial designs and methodologies. Drive innovation and regulatory compliance in drug development.
Senior Director Of Biostatistics
in Healthcare + Life Sciences PermanentJob Detail
Job Description
Overview
- Lead biostatistical strategies for clinical development phases I-IV, ensuring innovative methodologies and regulatory compliance.
- Collaborate with cross-functional teams to optimize clinical development plans aligned with corporate objectives.
- Provide strategic input into clinical trial design, statistical analysis, and interpretation of study results.
- Oversee statistical content for regulatory submissions and interactions with global agencies.
- Coordinate statistical endeavors with external organizations, CROs, and consultants.
- Implement emerging methodologies and innovative approaches in clinical development.
- Contribute to the development of departmental SOPs and best practices.
- Maintain a hybrid work environment with flexible on-site and remote arrangements.
Key Responsibilities & Duties
- Design and analyze clinical studies using advanced statistical methods to support drug development.
- Provide oversight for statistical content in regulatory interactions and submissions.
- Collaborate with senior members across functional areas for strategic planning.
- Coordinate statistical activities with external organizations, including CROs and consultants.
- Identify and implement innovative methodologies for clinical development.
- Participate in the establishment of departmental SOPs and operational standards.
- Oversee vendors to ensure program deliverables and timelines are met.
- Contribute to planning and preparation of regulatory submissions and integrated summary documents.
Job Requirements
- Ph.D. in Statistics or Biostatistics with 16+ years of clinical research experience.
- Expertise in neuroscience and methodologies for clinical trials and lifecycle management.
- Extensive experience with regulatory agency interactions, both US and international.
- Strong analytical skills for data interpretation and analysis in drug development.
- Excellent communication skills to convey statistical information to diverse audiences.
- Ability to adapt to changing priorities and work effectively under pressure.
- Willingness to educate internal teams on statistical methodologies.
- Domestic and international travel up to 15% as required.
- ShareAustin: