Associate Director, Biostatistics

Position Summary:

The Associate Director, Biostatistics is responsible for leading the development and execution of statistical aspects for global clinical programs.  He/she will provide project leadership and hands-on technical statistical support. This position reports to the Senior Director, Biostatistics.

Key Responsibilities:

• Independently lead the development and execution of all statistical aspects for one or more clinical development programs, including contribution to study trial design, analysis planning, study results presentation and interpretation, clinical study report authoring, regulatory submissions, and publications.
• Review or author statistical analysis sections of protocols, statistical analysis plans (SAP), clinical study reports (CSR), regulatory documents or scientific publications.
• Generates or reviews study randomization, sample size/power estimations and key specifications for statistical programming implementation of analyses including programming specifications for analysis datasets and TLFs, including SDTM and ADaM specifications.
• Manage biostatistics and programming vendors.
• Develop statistical programs to ensure quality and accuracy or to perform other pre-specified or ad-hoc analyses as required.
• Work as part of a collaborative, cross-functional team with members from other disciplines.
• Represent Biostatistics, ensuring statistical input is provided throughout the clinical development process.
• Interact with regulatory agencies, and effectively address statistical questions and requests.
• Take accountability for ensuring quality in all planning, design, and execution of assignments associated with the assigned protocol or project.

Qualifications:

• PhD or MSc in Biostatistics or related discipline, 8+ years’ experience working across all phases of clinical trials in CRO/Biotech/ Pharmaceutical company.
• Solid knowledge of statistical methodology, clinical experimental design and analysis for clinical trials.
• Experience working with CROs and vendors.
• Good knowledge of ICH, FDA, EMA, and NMPA guidelines.
• Prior experience supporting global clinical trials.
• Project leadership experience.
• Submission experience is strongly preferred.
• Exceptional interpersonal skills and problem-solving capabilities.
• Excellent oral and written communication skills and ability to effectively communicate statistical concepts to both technical and non-technical stakeholders.
• Experience working with cross-functional teams, including clinical development, regulatory affairs, medical affairs and commercial.
• Experience working with CDISC data standards.
• Proficiency in SAS programming and other statistical software tools.
• Fluency in both English and Mandarin Chinese, both oral and written communication.
• Comfortable working in a demanding, fast-paced, start-up culture with evolving processes. Flexible and able to adapt to new situations as the business demands.
• Demonstrates flexibility to work non-traditional work hours when needed, given international operations across time zones.

#LI-Hybrid

Zenas is committed to fair and equitable compensation practices. The base salary pay range for this role is $172,300 to 215,400. Actual compensation packages will depend on various factors, including, but not limited to depth of experience, education, skillset, overall performance and/or location.

Zenas believes in providing a competitive compensation and benefits package to all employees. Our base salary is just one component of Zenas’ competitive total rewards strategy that also includes annual performance bonus, equity, full range of benefits and other incentive compensation plans.