Executive Director, Medical Director - Waltham, United States - Dyne Tx

Description

Our commitment to people with muscle diseases

Dyne Therapeutics is a clinical-stage muscle disease company focused on advancing innovative life-transforming therapeutics for people living with genetically driven diseases.

With its proprietary FORCE platform, Dyne is developing modern oligonucleotide therapeutics that are designed toovercome limitations in delivery to muscle tissue.

Dyne has a broad pipeline for serious muscle diseases, including clinical programs for myotonicdystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD), and a preclinical program for facioscapulohumeral muscular dystrophy (FSHD).

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Role Summary:

The Executive Director, Clinical Development serves as a key member of the Company's Clinical Development and Program Team and will have primary responsibility for the design and oversight of an integrated development strategy, including both in-house development and potential strategic partnerships to augment the internally developed pipeline.

This position will provide comprehensive leadership of the development process from pre-IND studies through to NDA and Phase IV programs.

The Executive Director, Clinical Development will be responsible and accountable for the development of the medical aspects of the FSHD clinical program.

This role will be responsible for delivering quality and timely medical input and interpretation on specific program data in fulfilment of the program objectives, working in partnership with regulatory affairs and pharmacovigilance in providing medical support for pharmacovigilance activities, responses to regulatory agency queries, and development.

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

Primary Responsibilities Include:
Lead the FSHD Clinical Development teams across planning, design, development, and implementation of clinical trials for the drug candidate
Develop knowledge of disease mechanisms to select biomarkers, pharmacodynamic endpoints, and patient stratification considerations
Develop and implement an effective, timely and cost-efficient development program to establish the safety and efficacy of drug candidate compounds to achieve approval in the US and other countries
Develop protocols and study completion determinations
Coordinate with the discovery group to assure smooth transitioning of development candidates/programs from research into development
Provide pharmacovigilance oversight and manage timely reporting of safety signals to regulatory agencies
Guide Research team on decisions that have clinical components and implications
Identify, manage, and interface with external collaborators and key opinion leaders to create clinical development strategies for a novel class of therapeutics
Provide clinical development oversight for Discovery and Development programs, including strategy, planning, execution, and completion of clinical trials according to all applicable regulations and guidance
Collaborate with Clinical Operations to ensure all clinical study activities are completed in accordance with applicable regulations and guidance, maintaining the highest quality clinical programs, following GCP and ICH guidelines and the Company's standard operating procedures
Lead Clinical Development team meetings to ensure close collaboration and alignment with key cross-functional stakeholders
Represent the FSHD Clinical Development at internal leadership meetings to drive strategic decision making
Select between outsourcing and in-house approaches for Clinical Development capabilities and work closely with the Clinical Operations team to implement choices
Manage relationships with third parties, such as CROs and outside collaborative partners, who are part of the clinical development efforts
Serve as medical representative to regulatory agencies, our investigators, and advisors and as study medical monitor, as needed
Participate as requested in Business Development due diligence and presentations to external constituencies
Manage the writing of protocols, presentations, and publications (regulatory submissions, original peer-reviewed articles, abstracts)
Review key documents including protocols, investigator brochures, and informed consent forms
Maintain accountability for all relevant timelines and deliverables working closely with functional counterparts and colleagues on the integration of product and clinical development plans
Manage, coordinate, and provide ongoing assessment, evaluation, and communication with other departments and external vendors in order to ensure study objectives and timelines are accomplished
Support the Head of Development with oversight and management of the department budget and financial planning
Provide management personnel with timely updates on progress and changes in scope, schedule, and resources as required
Ensure compliance with all applicable regulatory standards related to global clinical trials and interactions with physicians
Develop and implement SOPs for clinical trials and related activities, as required
Interface with departments within and outside of R&D including Finance, Regulatory Affairs, Legal, and Medical Affairs
Develop and maintain professional relationships with academic and community-based study sites
Represent the company in interactions with regulatory agencies
Provide leadership and mentorship to clinical development team members, managing matrix and direct line reports

Education and Skills Requirements:
Doctor of Medicine degree, PhD or Pharm. D., with a strong scientific background and a specialty in neurology or neuroscience training highly preferred
Minimum of 15 years of pharmaceutical industry experience
Experience leading a clinical development program(s) in Neurology/ Neuromuscular disorders
Experience with all aspects of designing, executing, monitoring, and managing clinical trials from inception to completion across all phases of development
Robust regulatory experience with Pre-INDs, INDs, CTAs, EOP 2 meetings and NDA/BLAs/MAA, both US and ex-US
Experience managing significant accelerations and challenges in clinical programs
Significant experience in communicating/presenting key/complex information to department/functional lead(s)/senior management
Strong knowledge of FDA and ICH regulations
Thorough knowledge of clinical medicine, clinical pharmacology and associated disciplines
Expert knowledge of Good Clinical Practice (GCP)
Experience in a small to mid-sized biotech company is preferred
Proven track record of drug development with Phase 1 through 3 trial experience preferred
Readiness to "roll up the sleeves" to contribute to team efforts
Excellent writing skills with a track record of publications and polished presentation skills to influence internal and external audiences
Ability to develop creative approaches to processes, practices, services, business models, and strategy
Ability to translate basic science into a product development plan that will maximize the product's commercial opportunity
Ability to work successfully in a matrix environment and effectively build consensus
Communication skills (written and verbal), which are equally effective internally and externally, with large and small audiences, and one-on-one's
Ability to effectively lead cross-functional meetings, and meetings with senior leaders to drive successful outcomes
Ability to create and inspire high-performance clinical development team
Ability to drive key actions at a high level of independence, working with staff, other senior leaders and designated external constituencies as necessary
Ability to effectively plan near to long-term strategy to ensure that most important efforts are prioritized and driven aggressively
Takes personal accountability for outcomes and thrives on increasing levels of responsibility to move the business forward
Strong project planning, leadership, negotiation, communication, and presentation skills as well as a demonstrated ability to contribute creative yet practical solutions to problems
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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.

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