Associate Director / Director, Biostatistics

Company Overview

Immunome is a clinical-stage targeted oncology company committed to developing first-in-class and best-in-class targeted cancer therapies. We are advancing an innovative portfolio of therapeutics, supported by a leadership team with deep experience in the design, development, and commercialization of cutting-edge therapies, including antibody-drug conjugates. Our pipeline includes varegacestat, an investigational gamma secretase inhibitor for which an NDA has been submitted to the U.S. FDA; IM-1021, a clinical-stage ROR1 ADC; IM-3050, an IND-cleared FAP-targeted radiotherapy; and IM-1617, an IND-cleared solid tumor ADC. We are also advancing a broad portfolio of early-stage ADCs pursuing undisclosed solid tumor targets.

Position Overview

The Associate Director / Director, Biostatistics provides statistical support to clinical studies, including the design, analyses, and interpretation of clinical trials. This position collaborates closely with cross-functional teams and provides scientifically rigorous statistical expertise on projects and protocols in support of clinical development and for publication and presentation.

Responsibilities

• Apply rigorous statistical expertise to study design, statistical analysis plans, interpretation of results, project development plans, and regulatory issues.
• Provide strategic statistical input into clinical development plans and study-level decision-making, anticipating downstream regulatory and data implications to inform study design and overall development strategy.
• Plan, deliver, and communicate statistical analyses and scientific reports, including clinical trial and exploratory analyses, and support publications and scientific presentations.
• Own the timeliness and quality of study- and submission-level statistical deliverables on assigned projects. For outsourced studies, manage vendors and monitor their performance and adherence to project timelines.
• Ensure all study- and project-level statistical activities are conducted in compliance with relevant regulatory requirements (e.g., FDA regulations).
• Contribute to interactions with regulatory authorities (e.g., FDA, EMA), including statistical input for regulatory meetings, responses to health authority questions, and preparation for advisory committee meetings.
• Collaborate with internal partners (e.g., clinical development, clinical data management, statistical programming) to provide statistical support and help identify and resolve data issues.
• Develop and lead initiatives in process improvement, training, and standard development.
• Support ad hoc analyses and develop and validate programs for data analysis, reporting, and visualization.

Qualifications

• PhD or Master's in Biostatistics, Statistics, or a related field.
• A minimum of 6 years (with a PhD) or 8 years (with a Master's) of biostatistics experience supporting clinical trials in the pharmaceutical, biotech, or CRO industry, or equivalent.
• A minimum of 2 years of leadership or people-management experience is preferred.

Knowledge and Skills

• Prior oncology clinical trial experience, including familiarity with standard response criteria (e.g., RECIST 1.1), oncology endpoints (e.g., overall survival, progression-free survival, objective response rate), and associated statistical methodology (e.g., survival/time-to-event analysis, group sequential and adaptive designs).
• Experience supporting regulatory submissions (e.g., NDA, BLA) is a strong plus.
• Experience managing CROs and external statistical vendors, including oversight of outsourced statistical deliverables, is a plus.
• Proficiency in statistical programming languages (e.g., SAS, R); experience using simulation to support trial design is a plus.
• Knowledge of CDISC data standards (SDTM and ADaM).
• Knowledge of drug submission requirements and relevant ICH and FDA/EMA guidelines, including the ICH E9(R1) estimand framework.
• Strong verbal and written communication skills, including the ability to convey complex statistical concepts to cross-functional, non-statistical audiences.
• Strong problem-solving skills and the ability to work both independently and collaboratively in a fast-paced environment.
• Strong attention to detail and a proven ability to manage multiple competing priorities.

Washington State Pay Range- Associate Director: $200,850 - $227,316

Washington State Pay Range- Director: $235,000 - $263,700

Washington State Pay Range

$200,850 - $263,700 USD

E/E/O

Immunome, Inc. is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

E-Verify

Immunome, Inc. is a participant in E-Verify. Please review the following notices: E-Verify Participation Poster | Right to Work Poster (English) | Right to Work Poster (Spanish).