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Senior Medical Director – Neurology

Spark Therapeutics
Philadelphia, United Statesfull_timeVerifiedPosted 13 Oct 2024
💰 $353,500/yr($235,700/yr$353,500/yr)

About the role

Join the Spark Team

 

We were born of innovation, springing from the curiosity, imagination and dedication of remarkable scientists and healthcare visionaries. Our shared mission is to unlock the power of gene therapy to accelerate healthcare transformation. 

 

We don’t follow footsteps. We create the path.

 

 

Primary Duties

This individual will be directly, and through the team, responsible for developing global clinical strategies and providing clinical support for all neurology (and other therapeutic areas, as necessary) programs as Clinical Development Lead (eg, program/trial development, site selection and enrollment, investigator engagement, site training, clinical operations). This leader will develop plans that deliver medically differentiated therapies which provide meaningful improvements to patients. The Clinical Development Lead is a core member of the Asset/Life Cycle Team and is responsible for overseeing and developing global gene therapy development strategies and disease intervention strategies and ensuring their effective and efficient execution. The individual will guide the development of gene therapies and programs, approve Clinical Development Plans and priorities, and lead the design and final interpretation and completion of clinical studies. The individual as Clinical Development Lead will provide clinical development support and guidance into global regulatory interactions, will assist the Medical Affairs team, as necessary, and will provide clinical support for strategic planning activities (including clinical advisory boards). The individual will serve as a scientific, medical, and strategic expert both internally and externally.

 

Responsibilities

  • Plays a leadership role in providing clinical science and broader development input into the relevant therapeutic area clinical scientific strategy, as well as into relevant cross-functional and enterprise-wide plans, strategies and initiatives.
  • Leads global clinical strategy development for gene therapies in neuroscience.
  • Drives strategy and provide insight for potential new clinical programs and projects based on medical need and development requirements; leads the design of clinical programs and clinical study protocols and ensures timely execution of all neuroscience clinical programs.
  • Leads the Development Subteam, a strategic team that integrates functional perspectives to define and implement a robust and technically sound Clinical Development Plan to deliver innovative treatment options using an integrated gene therapy platform for patients suffering from CNS disorders.
  • Evaluates possible needs and oversees creation and implementation of companion diagnostic opportunities and plans in neuroscience gene therapy development plans.
  • Organizes and executes clinical advisory boards to enhance and focus scientific contents of the neuroscience programs in development.
  • Provides clinical guidance to other R&D and Technology groups as needed, eg, nonclinical support, subject eligibility, adverse events, investigator questions, regulatory requests, statistical analyses, study design and conduct.
  • Initiates and develops professional relationships with external therapy area experts, investigators, and consultants.
  • Oversees and serves as clinical liaison with investigative sites; engages and supports clinical trial sites, including education and training. Participates in site selection activities (including feasibility and initiation visits; other site visits as required) and other trial-related activities to safeguard enrollment targets and study timelines.
  • Serves internally as clinical development expert for global regulatory interactions; collaborate with Regulatory Affairs in planning regulatory strategy and communications.
  • Participates in development and review of clinical documents, including position papers, protocols, study reports, regulatory documents (eg, NDA, MAA responses,

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Company

Spark Therapeutics

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