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Job Description

Jumpstart is a program we initiated where we work with a variety of rare disease groups to help them establish a research agenda. We get many inquiries in the ODC about what a parent or foundation can do next to find a cure, and it all begins with research. Many of these diseases have no funding and little happening in terms of research toward drug development. We learn what exists in their disease space and identify what the appropriate next steps would be to initiate/progress research in their disease. In some cases, the conversation advances to a partnership with the ODC.

We are currently seeking a new Director of the Jumpstart Program that will directly impact the ODC's mission of developing transformative therapies using platform technologies that can be deployed across multiple rare diseases. As the Director of Jumpstart, you will be the main point-of-contact for all foundation and rare disease patient parents who are seeking guidance on their specific disease's research agenda. You will help them navigate what is their best next course of action for their disease. If fitting, you will assess the disease for potential partnership with the ODC, working with ODC leadership and adviser to develop a strategic plan for new R&D programs, including the establishment of centralized research tools across diseases. You will partner with the ODC program of excellence directors to build out best practices and resource planning across multiple rare disease programs. You will continue to expand the ODC's research network of Key Opinion Leaders, foundation partners, and patient groups as well as identify potential biopharmaceutical partners. Also, you will lead efforts for applying new platform technologies to specific rare diseases of interest.

Joining the ODC offers you with unique opportunity to contribute to revolutionizing the practice of medicine for under-served patient groups.

Qualifications:

⢠Highly advanced professional discipline. M.D., Ph. D., or equivalent doctoral degree and 5+ years of relevant experience is required.

⢠Research experience in Neuro-focused discipline and rare disease strongly preferred

⢠A Certification in Genetic Counseling (CGC) strongly preferred

⢠3-5 years of drug development experience

⢠Experience writing clinical development plans preferred

⢠Self starter but also a strong desire to contribute and work collaboratively to achieve goals

⢠Success in roles requiring execution of multiple tasks while responding to multiple priorities

⢠Highly functioning, detail-oriented, and analytical candidate who can think strategically

⢠Excellent oral/written communication skills required

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