Vice President, Medical Affairs, EMEA

Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role.   Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at ScholarRock.com and follow @ScholarRock and on LinkedIn. Summary of Position: Reporting to the SVP GM EMEA, the VP Medical Affairs EMEA will lead and oversee the company’s medical affairs strategy and activities across the EUR region and will be the “go to” medical person in EMEA for internal and external stakeholders. This role will be responsible for driving the EUR region medical strategy and excellence, supporting evidence generation activities, ensuring scientific communication, and fostering relationships with key opinion leaders (KOLs), and healthcare professionals (HCPs).  Working in a multifunctional, matrix organization with Global and US teams, you will ensure medical activities in the EUR region are aligned with overarching global strategies, goals and operations, as well as provide guidance and support to commercial and market access colleagues.   You will play a crucial role in shaping the company's medical footprint in the EUR region and ensuring alignment with regulatory, national payers, and healthcare organizations.  Position Responsibilities:

Serve as the EUR Responsible Scientific Officer 

Lead the development and execution of the EMEA medical affairs strategy in alignment with global objectives

Provide medical insights to support business and regulatory decisions

Collaborate with cross-functional teams (clinical development, clinical operations, regulatory affairs, commercial, and market access) to ensure scientific alignment and strategic focus.

Collaborate to develop medical strategy and content as appropriate for congresses, symposia and advisory boards and facilitate and execute such activities in Europe

Ensure the dissemination of accurate, balanced, and scientifically sound medical information

Lead the development and approval of region-specific scientific publications, presentations, and other communication materials

Delivers scientific presentations to diverse audiences (e.g. physicians, pharmacists, marketing/medical agencies, and other key stakeholders) in meetings, advisory and/or consulting settings

Represent the company at key scientific and medical conferences and engage with external stakeholders

Develop and maintain relationships with top regional KOLs, HCPs, and patient advocacy groups across Europe

Engage in meaningful dialogue with external experts to gather insights, feedback, and strengthen partnerships

Support the co-development and sign off of promotional materials and campaigns, in the prelaunch and the launch phase and set up appropriate medical review procedure to make such materials compliant in EUR

Indirect leadership to country medical affairs leaders

Provide medical support to clinical development and clinical research conducted in Europe such as the identification of medical centers of excellence and key investigators/sites in such programs, support operational tasks such as investigator meetings and targeted patient recruitment efforts

Continuously maintain deep scientific and medical knowledge of Spinal Muscular Atrophy and a deep understanding of patient and physician interactions and clinical decision making and impact

Assess medical education needs in Europe and develop internal and external educational strategy as needed

Provide EU region medical monitoring support for all clinical programs where needed

Coordinate investigator-initiated studies and foster collaboration with academic institutions

Ensure that all medical affairs activities are conducted in compliance with regional regulatory requirements, ethical guidelines, and company policies

Support regulatory submissions, product launches, and post-marketing surveillance activities

Lead and mentor a team of medical affairs professionals across the region

Foster a culture of continuous learning and development within the medical affairs team

Candidate Requirements:

MD (or equivalent), PhD, or PharmD required. Expertise in SMA is a plus

Minimum total of 10 years of experience in medical affairs and/or clinical development

Extensive experience in the biotech or pharmaceutical industry, particularly in rare diseases, and/or neurology (neuromuscular experience is a plus)

Excellent communication (both verbal and written), presentation, and relationship-building skills

Proven track record of successfully leading medical affairs strategies and teams and/or clinical studies at a regional level

Strong knowledge of the European healthcare landscape, regulatory environment, and market access challenges

Ability to interact with and build effective professional relationships with colleagues across functional areas. Demonstrate an exemplary ability to develop and maintain relationships with external colleagues, partners/ stakeholders

Experience and success in working in a matrix, cross-functional environment; excellent collaboration skills; experience working across functions to achieve results

Ability to work effectively in a fast paced, innovative and rapidly changing environment, while remaining flexible, proactive, resourceful and efficient

Outstanding work ethic and integrity, including high ethical and scientific standards

Strong interpersonal skills particularly motivational, negotiation, listening, judgment, analytic, and conflict management skills

Fluency in English; proficiency in additional European languages is an asset

Ability to travel across Europe as needed.