Sr Medical Science Liasion (Contract)

The Opportunity: REGENXBIO is an exceptional place where some of the best of brightest people have the opportunity to collaborate, touch amazing science, and contribute toward extraordinary plans. As a Contract Medical Science Liaison, Rare Diseases you will provide support for REGENXBIO Rare Disease pre-commercial clinical trials and scientific collaborations with a focus on our Duchenne muscular dystrophy development program. This is an exciting opportunity for an innovative MSL with an entrepreneurial spirit who enjoys building networks, interacting with KOLs, conducting scientific exchange, and supporting scientific conferences. This is a 6-month contract position with the potential to convert to permanent.

What you'll be doing:

• Support clinical trial recruitment and site outreach; communicate coordinated feedback to the Clinical Operations, Clinical Development, and Duchenne Core teams.
• Serve as the field-based Medical Affairs representative to establish and cultivate scientific relationships with KOLs in the Duchenne community.
• Develop a strong understanding of clinical practice as it relates to Duchenne. 
• Participate in refining KOL mapping; develop and execute on a customer-centric tactical engagement plan to support Medical Affair's strategies.
• Gather and share scientific insights via scientific exchange to inform executable and innovative Medical Affairs strategies.
• Serve as a resource for addressing unsolicited medical questions about REGENXBIO’s trials and investigational products.
• Provide clinical expertise in the development, management, and maintenance of clinical and scientific communications, including educational materials, meeting presentations and FAQs. 
• Attend medical conferences as MA representative:  assist with congress strategy / planning, medical booth staffing, competitive intelligence / insights gathering, and generating meeting summaries.
• Support Patient Advocacy conferences and outreach as requested.

What we're looking for:

• Master’s degree (MPH or equivalent) required. Doctorate level (MD, PharmD, PhD) preferred.
• Minimum of 3 years of rare disease clinical or therapeutic experience in neuromuscular diseases, and/ or gene therapy strongly preferred.
• 3-5 years of MSL experience in rare disease state with primary emphasis on field based scientific exchange and/or clinical trial support.
• Superior communication, relationship building and interpersonal skills.
• Ability to assimilate new clinical data quickly.
• Proactive problem-solving skills.
• Project management and medical writing skills.
• Flexibility, resilience, and creativity/ innovation in their work 
• Ability to organize and lead high level projects.
• Ability to proactively predict issues and solve problems.
• Ability to work collaboratively with cross-functional teams.