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Associate Medical Director/ Medical Director, Medical Affairs - Rare Disease

Company: REGENXBIO
Location: Rockville
Posted on: September 12, 2020

Job Description:

Associate Medical Director/ Medical Director, Medical Affairs - Rare Disease  About the Organization REGENXBIO is a leading clinical-stage biotechnology company seeking to improve lives through the curative potential of gene therapy. REGENXBIO's NAVĀ® Technology Platform, a proprietary adeno-associated virus (AAV) gene delivery platform, consists of exclusive rights to more than 100 novel AAV vectors, including AAV7, AAV8, AAV9 and AAVrh10. REGENXBIO and its third-party NAV Technology Platform Licensees are applying the NAV Technology Platform in the development of a broad pipeline of candidates in multiple therapeutic areas.

Our gene therapy product candidates are designed to deliver genes to cells to address genetic defects or to enable cells in the body to produce therapeutic proteins that are intended to impact disease. Through a single administration, our gene therapy product candidates are designed to provide long-lasting effects, potentially significantly altering the course of disease and delivering improved patient outcomes. We are currently developing gene therapy product candidates for the treatment of retinal, metabolic, and neurodegenerative diseases. Our product candidates all utilize AAV viral vectors from our proprietary gene delivery platform, which we call our NAV Technology Platform. In addition to our internal product candidate programs, we also selectively license our NAV Vectors to other leading biotechnology companies.

Req Number CLI-19-00015

Description POSITION SUMMARY

The Associate Medical Director/ Medical Director, Medical Affairs (MA)- Rare Disease is an in-house position that is based in Rockville, MD. Reporting to the Senior Director, Head of Medical Affairs, the incumbent will assist in developing Medical Affairs strategy, manage and support MA projects, help with development of publications, presentations and MA deliverables, provides project management support, assists with MA research projects (such as natural history studies, registries, research collaborations), execute advisory boards, and managing KOL advisors. Position is focused in Rare Disease with opportunities to cover other therapeutic areas.

Position Requirements PRIMARY RESPONSIBILITIES

Develop and implement MA strategy and plans including field medical plans, to support overall corporate objectives.

Build relationships with thought leaders, clinical investigators, and other healthcare professionals /stakeholders, including patient groups and professional organizations.

Provide medical leadership, insight and strategy through collaborations with other internal functions and project teams (i.e. Commercial, Clinical, Operations, Regulatory, Biostatistics, Project Management, and Patient Advocacy).

Develop relationships with and manage KOL advisors- develop strategy, draft scope of work, contracts, meetings, advisory boards, invoicing and payments.

Attends medical conferences as MA representative, assists with congress planning and strategy, leads meetings and assists with meeting summaries.

Assists with publication strategy across products- abstract planning, timeline management, presentation, poster, and manuscript development.

Identify and implement appropriate high-impact medical research projects to support the business objectives, including company -sponsored and investigator-initiated projects.

Provide support for the development, review and approval of presentation materials for scientific meetings, conferences, and other publicly distributed materials.

Supports Clinical Development on strategy, background research and problem solving.

Participates in competitive intelligence and/or other market/industry assessment activities and projects and developing internal FAQs.

Maintains scientific and clinical knowledge in the specific disease area(s) and serve as key medical resources in the disease area and on specific products.

Provide strategic input and training to the Medical Affairs organization.

SKILLS, KNOWLEDGE AND ABILITIES REQUIRED

Doctorate level degree required (MD, PharmD, PhD, or equivalent) with 3 or more years of relevant clinical or therapeutic experience (preferred),

Minimum 3-5 years Medical Affairs relevant experience within the pharmaceutical industry.

Therapeutic area expertise preferred in: Rare Disease, Neurology and/ or gene therapy.

TECHNICAL SKILLS

Superior medical writing, project management, communication, interpersonal and negotiating skills.

Ability to lead and manage high level projects.

Ability to proactively predict issues and solve problems.

Ability to drive decision-making within a multi-disciplinary team.

Diplomacy and positive influencing abilities.

Ability to manage multiple projects and vendors when necessary.

WORKING CONDITIONS AND/OR PHYSICAL REQUIREMENTS

Ability to travel 25%.

MANAGER/SUPERVISORY RESPONSIBILITIES

None

Location Rockville, Maryland

Exempt/Non-Exempt Exempt

EOE Statement We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, national origin, disability status, protected veteran status or any other characteristic protected by law.

Open Date 8/9/2019

This position is currently accepting applications.

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Keywords: REGENXBIO, Rockville , Associate Medical Director/ Medical Director, Medical Affairs - Rare Disease, Other , Rockville, Maryland

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