Senior Director, Biostatistics

Kite Pharma•Parsippany, NJ

1d•$237,575 - $338,250•Remote

About The Position

We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet. Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows. Reporting to the Kite Head of Biometrics, the Senior Director of Biostatistics will play a leading role in contributing to short- and long-term Biostatistics strategies, product development plans, global submission plans and infrastructure development that cut across all Development functions and workstreams. May be responsible for a team supporting multiple disease areas, a whole therapeutic area, or another significant area within Biometrics. Routinely consults with executives to help envision future direction and prioritize investment and other key strategic business decisions. The ideal candidate will have a proven track record of functional leadership, strategic situational judgment in using both innovative and pragmatic statistical methods, as well as demonstrated motivation for and excellence in people management and development. Position can be remote or may be office-based in Foster City, CA, El Segundo, CA, Thousand Oaks, CA, or Parsippany, NJ.

Requirements

12+ years with MS/PhD
14+ years with BA/BS
In-depth knowledge of the drug development process, with strong commitment to Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements.

Nice To Haves

15+ years (MS) or 12+ years (PhD) of progressive industry experience in biostatistics, with a proven record of advancing the statistical analysis of biomedical data in complex development environments.
Demonstrated experience leading Biostatistics strategy for product development in hematologic malignances (including multiple myeloma) and solid tumors; in particular, for cellular and/or gene therapies.
Demonstrated leadership relating to Regulatory submission strategy, including advisory committees or oral explanations.
Expert-level knowledge of the Biostatistics field and its evolving landscape, including a track record of publications.
Proven ability to define and operationalize short- and long-term Biostatistics strategies, driving impactful decisions across therapeutic areas and enterprise initiatives.

Responsibilities

Play a leading role in contributing to short- and long-term Biostatistics strategies, product development plans, global submission plans and infrastructure development that cut across all Development functions and workstreams.
May be responsible for a team supporting multiple disease areas, a whole therapeutic area, or another significant area within Biometrics.
Routinely consults with executives to help envision future direction and prioritize investment and other key strategic business decisions.
Demonstrates exceptional verbal and written communication skills, with the ability to effectively engage, influence, and align stakeholders at all organizational levels.
Applies a strong understanding of regulatory requirements and statistical principles to ensure alignment with regulatory expectations and to support the achievement of scientific and business objectives.
Exhibits strong leadership, critical thinking, and strategic acumen, translating complex scientific and business challenges into clear direction and actionable plans.
Directs complex, multi-functional programs and initiatives, driving the integration, interpretation, and strategic use of data from diverse internal and external sources.
Serves as a trusted advisor and key contributor to senior leadership, providing strategic input on departmental and enterprise-level initiatives.
Develops deep subject-matter expertise within a therapeutic area, indication, or technical discipline, and is recognized as a enterprise-wide resource in that domain.
Communicates scientific and statistical concepts with clarity and impact, leveraging a range of platforms to effectively influence both internal and external audiences.
Collaborates extensively across Development and other functions to drive cross-functional alignment, decision-making, and execution.
Influences outcomes by effectively engaging peers, cross-functional partners, and leadership, driving consensus and advancing strategic priorities.
Oversees and directs a large, complex portfolio of programs and projects, potentially spanning multiple disease areas.
Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams.
Develop Talent - understand the skills, experience, aspirations and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop and realize their purpose.
Empower Teams - connect the team to the organization by aligning goals, purpose, and organizational objectives, and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem.