Senior Director, Biostatistics

Cellectis Careers • New York, NY

129d • $220,000 - $240,000

About The Position

The Senior Director, Statistics will be in charge of the development and oversight of biostatistics and statistical/clinical programming strategies, operations, and personnel to ensure the efficient, accurate and timely collection and analysis of clinical trial data while ensuring high standards of data integrity and quality. The Senior Director Biostatistics will partner with other company leaders to design and implement clinical development plans, and overall development strategy for Cellectis’ programs and products. The incumbent will manage and direct CRO partners and leverage the capabilities of these partners. This role is an experienced leader comfortable liaising with senior levels of management both within and external to the organization.

Requirements

• Masters in Statistics or Data Sciences preferred
• Minimum 15 years of experience in leading biostatistics in clinical research (at various levels and in different capacities), including having built the biostatistics function and 5 years managing a biostatistical group working on all phases of clinical research and drug development
• Experience with an NDA/EMA filing supporting US as well as international trials
• Extensive experience in pharmaceutical or biotech companies determining appropriate designs, understanding the science and clinical application and analyses for clinical trials
• Demonstrated experience building and managing a biostatistics team as well as using and managing outside consultants/CRO’s a must, including proficiency in project planning and management and proactively anticipate and identify complex issues and problems
• Demonstrated high level of technical skill and expertise as pertains to biostatistics, and programming, with an understanding of data management and data flow
• Demonstrated excellent decision-making abilities with competency in making decisions and resolving problems
• Successful track record of the management of clinical studies, from Phase I – III in support of US NDA filings
• Proven track record communicating and leading the Biometrics discussions with the FDA, EMEA and other Global Health Authorities

Responsibilities

• In collaboration with the company leaders, create and implement development strategies consistent with the company’s strategic objectives
• In collaboration with functional leads, ensure that the design of clinical trials and overall development plans are strategic, creative and meet requirements of global regulatory authorities with a high probability of technical success
• In collaboration with functional leads, ensure that the execution of clinical trials, (specifically data capture, cleaning) delivers quality and timely ongoing and final databases, develop strategies to minimize the cost of clinical trial execution in delivering quality clinical trial data and ensure that clinical trial systems used in the running of clinical trials are effectively linked to avoid conflicting information.
• Effectively and efficiently manage CRO partners in the execution of statistical aspects of ongoing and planned clinical trials
• Partner with member of study management teams and clinical science teams
• Ensure the overall effective operations of the biostatistics, clinical data management, and clinical/statistical programming
• Provide expert drug development advice to teams and development leaders
• Establish a company environment that benefits from biostatics and quantitative sciences as strategic contributors in making assessments and decisions
• Oversee and build the biometrics function, ensuring systems, capabilities, and resources are in place (both internal and external) to optimize the design, collection, analysis, and interpretation of data for each program consistent with the company’s strategic objectives
• Develop and implement the statistical and data management specific standards, processes, SOPs, training and quality control for oversight of the biometrics activities in compliance with ICH and GCP in support of an internal and external resourcing model
• Support the Regulatory head in interacting with FDA and other regulatory authorities to ensure clinical studies meet regulatory requirements and to ensure ongoing agreement on project development
• Partner with company leaders in building critical trial execution processes within and across functions to ensure GCP readiness and establish standards for teams to follow
• Accountable and responsible for external biostatistics and program deliverables for CSRs and submission documents from CROs
• Responsible for ensuring that the biostatisticians design and generate analyses in support of early phase studies as well as for abstracts and publications
• Interact with FDA and other regulatory authorities to ensure clinical studies meet regulatory requirements and to ensure ongoing agreement on project development

Benefits

• Anticipated compensation, DOE, $220,000 - $240,000

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Master's degree