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Job description
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JOB DESCRIPTION
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.
Position Summary
JOB DESCRIPTION
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.
Position 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
Education And Experience
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
xtensive 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
CORE COMPETENCIES
Knowledge of GCP, ICH, and other Guidance documents and policies related to clinical trials operations requirements
Broad therapeutic understanding
Thorough knowledge of pharmaceutical and regulatory requirements, procedures, and policies
Exceptional interpersonal skills and written and verbal communication ability with demonstrated fluency in written and spoken English
Ability to make high level decisions and work with others as a team
Ability to travel up to 20%
Physical Requirements
Sedentary - primarily involves sitting and/or standing.
Communicates with others on a daily basis to exchange information.
Anticipated compensation, DOE, $220,000 - $240,000
Seniority level
Seniority level
Director
Employment type
Employment type
Full-time
Job function
Job function
Research, Analyst, and Information Technology
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Worksite address
new york, NY, 10261, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.