Associate Director, Biostatistics

Imagine yourself at the forefront of medical innovation, shaping the future of cancer treatment from anywhere in the world. Here at RayzeBio, a dynamic subsidiary of Bristol Myers Squibb, we’re fueled by a pioneering spirit and a shared mission to develop life-changing radiopharmaceutical therapies. We are actively seeking a talented Associate Director, Biostatistics to join our growing team. This is a fully remote, worldwide opportunity for someone ready to make a significant impact on our science, our teams, and most importantly, on patients' lives.

Overview

RayzeBio is truly unique, combining the agility of an emergent biotech with the extensive resources and global reach of a leading pharmaceutical innovator in oncology. Headquartered in San Diego, CA, our company is dedicated to improving patient survival by harnessing the transformative power of targeted radioisotopes. We are developing innovative drugs against challenging solid tumors. As an Associate Director of Biostatistics, you will play a pivotal role in the design, analysis, and reporting of our clinical trials, helping us bring novel treatments to those who need them most. Your expertise will be critical in advancing our mission to become the global leader in radiopharmaceuticals, all while working remotely from any location globally.

Key Responsibilities

Lead the statistical aspects of clinical studies, from early phase development through regulatory submission and post-market activities.
Collaborate closely with clinical development, regulatory affairs, data management, and medical writing teams to ensure statistical integrity and scientific rigor.
Develop comprehensive statistical analysis plans (SAPs), ensuring alignment with study protocols and regulatory guidance.
Perform complex statistical analyses using appropriate software and methodologies, interpreting results clearly and effectively.
Contribute significantly to clinical study reports, regulatory submissions, and scientific publications.
Represent Biostatistics in internal and external meetings, including interactions with regulatory agencies globally.
Provide statistical expertise and guidance to cross-functional teams, fostering a data-driven decision-making culture.
Participate in the evaluation and implementation of new statistical methods and software to enhance efficiency and quality.

Requirements

Doctoral degree (PhD) or Master's degree (MS) in Biostatistics, Statistics, or a closely related quantitative field.
A minimum of 8 years of experience for a PhD, or 10 years of experience for an MS, in the pharmaceutical or biotechnology industry, with a strong focus on clinical trials.
Demonstrated leadership experience in biostatistics, including leading projects, mentoring junior statisticians, or managing external vendors.
Proficiency in statistical programming languages such as SAS and/or R.
Solid understanding of clinical trial design, statistical methodologies, and regulatory requirements (e.g., FDA, EMA, ICH guidelines).
Experience in oncology drug development is highly preferred.
Excellent communication skills, both written and verbal, with the ability to convey complex statistical concepts to non-statisticians.
A proactive and collaborative approach to problem-solving within a fast-paced, innovative environment.

What You'll Gain

Joining RayzeBio means more than just a job; it’s an opportunity to contribute to truly transformative science within a collaborative and supportive environment. You will gain invaluable experience working on cutting-edge radiopharmaceutical therapies, supported by the extensive resources of Bristol Myers Squibb. Expect to accelerate your career, expand your expertise, and directly impact patient outcomes. We offer a competitive compensation package and the flexibility of a fully remote role, allowing you to thrive professionally and personally from anywhere in the world.