Associate Director, Biostatistics - Dyne Therapeutics

Dyne Therapeutics is focused on discovering and advancing innovative life-transforming therapeutics for people living with genetically driven neuromuscular diseases. Leveraging the modularity of its FORCE™ platform, Dyne is developing targeted therapeutics that are designed to overcome limitations in delivery to muscle tissue and the central nervous system (CNS). Dyne has a broad pipeline for neuromuscular diseases, including clinical programs for myotonic dystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD) and preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease.

Role Summary:

The Associate Director, Biostatistics will provide leadership and guidance for assigned clinical studies within a clinical development program(s). He/she will be responsible for or contribute to statistical activities including: designing innovative clinical trials, authoring statistical sections of protocols, preparing statistical analysis plans, ensuring quality in implementation of statistical analysis, interpreting and communicating the results of statistical analysis of clinical trial data in support of regulatory submissions as well as manuscripts. The ideal candidate must be a good communicator, exhibit high-energy, self-motivation, and forward-thinking. Experience working in rare disease is desirable.

This role is based in Waltham, MA without the possibility of being a remote role.

Primary Responsibilities Include:

• Serve as biostatistics lead for assigned clinical studies
• Effectively interact with members in other functions including medical, regulatory, safety, clinical operations and translational medicine for planning to ensure optimized delivery of clinical study activities
• Work collaboratively with internal and external (e.g., CRO) team members to coordinate the planning and execution of statistical deliverables
• Contribute under supervision to clinical protocol development, including authoring of the Statistics section and reviewing of other sections by applying statistical principles
• Design and specify stratification /randomization schema; review and approve test randomization lists
• Collaborate with Data Management, Clinical Development and Clinical Operations on design and review of eCRFs, and ensure data collection meet the requirements of statistical analyses
• Author or contribute to the development of statistical analysis plans for clinical trials, and for integrated summaries of safety/effectiveness (ISS/ISE) under supervision as necessary
• Provide guidance to statistical programmers on SDTM/ADaM and draft (or oversee) the development of shells for tables, figures and listings (TFLs)
• Provide statistical input, under supervision) to data monitoring committee (DMC) charters, independent review charters, and other study-level documents
• Provide statistical review of statistical deliverables (e.g ADaM datasets, TFLs)
• Contributes to clinical study reports, and other regulatory documents as required e.g. DSURs, Briefing Documents, etc.
• Perform ad hoc and exploratory statistical analyses as needed
• Assist, under supervision, in assigned statistical activities in support of IND/NDA/MAA or other regulatory submissions
• Assist in addressing statistical questions/comments from FDA and other regulatory agencies, and review and address comments by IRB/ECs
• Support and contribute to the preparation of publications, including manuscripts, posters and oral presentations
• Contribute to standardization and process improvement efforts for Biostatistics function

Education and Skills Requirements:

• Ph.D. or Masters in statistics or Biostatistics or equivalent with at least 8 years of experience in the pharmaceutical or biotech industry desired
• Interest in and basic understanding of biology and biological process including ASO and siRNA
• Experience in the design, analysis and reporting of clinical trials
• Experience in NDAs, MAAs or other regulatory submissions desirable
• Knowledge of statistical methods for clinical trials, including both frequentist and Bayesian approaches
• Knowledge of FDA, EMA and ICH regulations and guidelines
• Proficient in statistical programming (SAS is required and R is a plus)
• Experience with trial design software (e.g., EAST)
• Ability to concurrently lead statistical efforts for multiple studies desirable
• Understanding of data standards, including SDTM and ADaM
• Adept at overseeing statistical services provided by CRO’s and/or contractors
• Ability to work independently and act with initiative to address issues
• Ability to effectively communicate statistical concepts in a clear and concise manner both written and verbally.

The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.  Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.

This description is not intended to be constructed as an exhaustive list of duties, responsibilities, or requirements for the position. This position may change or assume additional duties at any time.  The employee may be requested to perform different or additional duties as assigned. All Employees are expected to adhere to all company policies and act as a role model for company values.

Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.