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:
Position Responsibilities
Serve as a thought leader on regulatory affairs, defining global regulatory strategy and plan to maximize regulatory success.
Serve as the global regulatory lead, providing strategic and operational input on assigned clinical and/or pipeline programs, such as the subcutaneous (IV to SC) and OPAL (<2 years old) program teams to achieve program objectives while ensuring compliance with applicable regulatory requirements in the region.
Be responsible for leading the global supplemental/type 2 variation filing lead for OPAL (<2 years old)
Develop regulatory roadmap to inform and guide agency engagement strategy; partner with key stakeholders to develop and implement a comprehensive regulatory engagement plan
Lead and managing regulatory interactions on assigned programs, building trusted relationships with regulatory authorities
Lead cross-functional effort to ensure timely submission of key regulatory documents (e.g., Module 1, briefing documents)
Ensure program team members and cross-functional stakeholders are informed of internal and external events that may impact regulatory success
Identify regulatory risks and opportunities and work with key stakeholders to develop solutions
Partner with global market access and medical affairs colleagues to support interactions with joint regulatory/health agency/HTA bodies on product specific value evidence topics, as applicable
Partner with Global and local Marketing/ Commercial as needed to align Regulatory Plan and Marketing/Commercial plan
Ensure strong representation of regulatory voice at key governance bodies and teams (e.g., DRC, program teams, clinical development teams, study teams)
Maintain currency of regulatory requirements and approvals to inform regulatory strategies and drive proactive plans to ensure compliance
Monitor and analyze global and country specific regulatory landscape to assess potential impact on the program; collaborate with teams to ensure compliance
Provide support to local regulatory experts
Provide regulatory support for cross-functional activities (e.g., SOPs, business development, clinical labeling, disclosure) as needed
Candidate Requirements
Education in life sciences required
Greater Boston-based with ability to be regularly present in the Cambridge, MA office
7+ years of experience Regulatory Affairs in biopharmaceutical industry with deep understanding of EU regulatory requirements
Demonstrated experience of leading successful engagement with EMA
Expertise and experience with biologics (particularly monoclonal antibody therapeutics) and rare diseases strongly preferred but not required
Demonstrated reputation as a well-respected, dynamic team leader with strong leadership and people management skills
Strong written, verbal communication skills, and interpersonal skills
Capable of managing shifting priorities in a rapidly changing and environment
Ability to travel domestically and internationally (~10%)
Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
