US Medical Director Neuromuscular presso Scholar Rock
Scholar Rock · Cambridge, Stati Uniti d'America · Hybrid
- Ufficio in Cambridge
Position Responsibilities:
- Strategic ownership of US Medical Plans – pre and post launch
- Organize external expert advisory boards, support scientific symposia, develop medical congress engagement strategy
- Act as medical lead for medical legal review committee (MLR)
- Analize medical insights to inform cross-functional strategies and tactics
- Collaborate with cross-functional field teams to identify data and educational gaps
- Provide strategic input for the development of educational and messaging
- Lead the digital medical education strategy and execution
- Continuously raise the bar for our externally facing materials, ensuring alignment to strategy
- Oversee Medical activities related to review of promotional and scientific materials
- Collaborate with functional groups as subject matter expert including Patient Advocacy, Commercial Operations, New Products, and many other internal stakeholders in support of pipeline products
- Provide medical leadership to guide internal and external decision-making
- Establish and maintain strong knowledge in SMA to optimize clinical study protocols development and execution
- Establish and maintain strong relationships with experts in the field, academics and professionals
- Ensure a patient-centric approach to development of clinical studies under her/his supervision
- Collaborate cross functionally to execute the clinical studies under her/his responsibility in alignment with the Brand plan and Global Medical Plan
- Collaborate with Global Medical to identify and execute internally and externally sponsored studies
- Foster strong relationships with internal and external stakeholders to identify unique opportunities to improve and evolve educational and training content.
- Manage budget for assigned projects.
- Travel required, comprising approximately 20%
Basic Qualifications:
- MD, PharmD, PhD or equivalent scientific degree. MBA desirable
- Minimum 5 years’ experience in industry R&D or Medical
- Excellent written and communication skills, highly organized and able to manage supporting multiple initiatives
Preferred Qualifications:
- Scientific communication and presentation skills with the ability to present scientific data in a credible manner. Able to interface professionally with a wide spectrum of internal and external academicians, in the scientific/medical arena
- Leadership skills; personal style that includes a sense of urgency, as well as flexibility and ability to respond to rapidly changing environments and circumstances
- Collaborative and proactive, with a hands-on, roll-up-the sleeves style and attitude
- Highest integrity; committed to ethics and scientific standards
- Solid track record of achievement in Medical Affairs in the biotech/pharma industry.
- Ideally have worked in the field of rare diseases; SMA experience would be advantageous.
- Launch experience is critical for this role
- Field experience is helpful
- Experience in clinical trial design, especially phase IIIb-IV
- Demonstrated successful partnership with Commercial organization, developed KOL programs and relationships, offered field training, patient outreach programs and the like.
- A curious learner who is focused on patient outcomes and values collaboration and advancing scientific understanding
- Be a critical thinker, able to share fact-based opinions without ego.
- Able to make complex science understandable for a non-scientific audience.
- Results-oriented, can embrace a fast-paced “can do” culture.
- Have scope for personal growth and development.