Senior Director of Biostatistics

Das ist der Job

Guide clinical and regulatory strategies to optimize trial design and maximize the probability of success.

Darum lohnt es sich

About the Position Formation Bio is seeking a highly skilled and experienced Senior Director, Biostatistics to join our dynamic team.

This critical role will report to the Head of Biometrics and will be responsible for leading and developing the biostatistics team and strategy, driving impactful statistical initiatives, and leveraging biostatistics to advance our drug development processes.

Responsibilities Strategic Leadership : Lead and develop the Biostatistics team, fostering a high-performance culture aligned with Formation Bio’s mission and values. Provide mentorship and career development to ensure team growth and expertise.

Regulatory & Cross‑Functional Collaboration : Partner with Clinical, Data Science, Regulatory, and Business Development teams to support drug diligence, development and regulatory interactions, FDA briefing books, and submission‑related activities. Proven experience leading biostatistics teams and strategies within clinical development.

Ability to collaborate cross‑functionally with Clinical, Data Management, Programming, Data Science, Regulatory, and other teams. The Senior Director, Biostatistics will play a key role in shaping innovative trial designs, supporting regulatory strategies, and ensuring high-quality statistical contributions across clinical development.

They will also collaborate cross‑functionally to integrate advanced analytics, data‑driven decision‑making, and AI applications into our development programs to improve efficiency and increase the probability of success.

Statistical Strategy & Innovation : Drive statistical strategy across clinical development programs, incorporating optimal trial designs, simulation-based approaches, and AI/ML applications to enhance efficiency and decision‑making.

Study Design & Execution : Provide expert statistical input into clinical study design, endpoint selection, analysis planning, and regulatory interactions. Explore innovative trial design options to identify the most effective clinical development strategy that aligns with business needs and optimizes decision‑making.

Ensure study designs are scientifically rigorous, operationally feasible, and aligned with regulatory expectations. Leverage AI‑driven clinical trial automation to enhance study execution, optimize resource allocation, and improve trial efficiency.

Represent Biostatistics in key regulatory meetings (e.g., FDA, EMA) to ensure statistical rigor in clinical development plans. Operational Excellence : Establish and refine statistical workflows, SOPs, and best practices to improve efficiency, quality control, and compliance with industry standards.

Data‑Driven Decision‑Making : Champion data‑driven approaches and quantitative decision‑making frameworks, integrating scenario analyses and statistical trial simulations to optimize clinical trial execution and strategic development plans.

External Engagement : Stay at the forefront of industry trends and regulatory expectations, representing Formation Bio in scientific discussions, conferences, and collaborations.

Vendor & CRO Management : Oversee and manage statistical vendors, including consulting statisticians and CROs, ensuring high‑quality statistical deliverables and compliance with GCP and regulatory standards.

About You Ph.D. in Biostatistics, Statistics, or a related field with 10+ years of experience in biostatistics within the pharmaceutical or biotech industry, statistical consulting firms, or CROs supporting clinical development.

Deep expertise in statistical trial designs, adaptive designs, Bayesian methods, and simulation-based approaches for both early and late‑stage development. Strong understanding of regulatory guidelines for drug development, including FDA and EMA requirements for statistical practice, regulatory submissions, and health authority interactions.

Experience in quantitative decision‑making frameworks to support internal Go/No‑Go decisions. Demonstrated track record of leading statistical contributions to progress assets from diligence, early development through regulatory submissions and approvals.

Strong problem‑solving skills with the ability to balance scientific rigor with operational efficiency. Excellent communication skills, with the ability to convey complex statistical concepts into actionable insights for non‑statisticians, senior management, and regulatory agencies.

Proficiency in SAS, R (S‑Plus), and statistical software for sample size calculations (e.g., East, PASS, NQuery). Expert R programming skills are a plus. Passion for innovation, AI‑driven methodologies, and data‑driven decision‑making in clinical development.

Compensation Salary ranges are informed in part by geographic location, in addition to other factors.

The target salary ranges for this role are: NYC Metro Area, Boston Metro Area, SF Bay Area : $275,000 - $340,000 All Other Eligible Remote Locations : $262,000 - $323,000 Eligible Remote Locations: Alabama (AL), Arizona (AZ), California (CA), Connecticut (CT), Florida (FL), Georgia (GA), Illinois (IL), Indiana (IN), Maryland (MD), Massachusetts (MA), New Hampshire (NH), New Jersey (NJ), North Carolina (NC), Ohio (OH), Pennsylvania (PA), South Carolina (SC), Texas (TX), Utah (UT), Virginia (VA), and Washington, D.C. (DC).

You will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. #LI-hybrid #J-18808-Ljbffr