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 and follow and on .
Summary of Position:
Under the supervision of the Director of Pharmacovigilance (PV) Operations, the Sr. Manager/Associate Director, Pharmacovigilance Operations will support day-to-day Scholar Rock Safety Operations activities. The individual will provide oversight and management of vendors, business partners, contracting and Individual Case Safety Report (ICSR) activity, as applicable, to ensure efficiency, quality, and compliance with internal procedures and global regulations. They will also contribute to compilation of metrics, support daily/weekly Department meetings and support individual study teams and collaborate on the support of risk management and pharmacovigilance activities for all Scholar Rock products. Additionally, they will contribute to the planning, execution, and implementation of process improvements, procedures, and solutions related to Scholar Rock pharmacovigilance and ICSR and Aggregate reporting.Position Responsibilities: Oversees PV vendors/service providers to ensure that they fulfill their accountabilities and responsibilities for all outsourced PV activities – case processing and reporting Participates in study activities as a PV Project Manager, from study start-up through conduct and study wrap-up. Serves as operational safety lead on all relevant study-related activities, attends routine and ad-hoc study meetings, establishes, maintains and executes roles within the Safety Management Plans/Expedited and Periodic Safety Reporting PlansActs as a Subject Matter Expert (SME) regarding the processing and reporting of Individual Case Safety Reports (ICSRs) for Scholar Rock products and participates in meetings with outsourced vendorsContributes to maintenance of metrics, Key Performance Indicators (KPIs) and related quality activitiesAssists in preparing, facilitating and documents Department activities, including weekly Safety team meeting, and other ad hoc discussions and decision, as applicableSupports and/or contributes to Departmental Inspection readiness, where applicable, including but not limited to author/contribute to controlled document preparation and administratorSupports budget/contract review process, serving as administrator, negotiator, QC, as directedAssists in maintenance of Department archive of safety documents, including relevant communications and other key documents Supports safety-governance-related activities, including scheduling and documentation, where applicable, of Product Safety Committee (PSC), Executive Safety Committee (ESC) or ad-hoc meetings Collaborates with and provides pharmacovigilance guidance and support for interdepartmental and/or corporate initiativesCollaborates with corporate partners to ensure proper exchange of drug-safety data, developing associated plansCandidate Requirements: Bachelor’s degree (preferably in a science or health-related field) and a master preferredA minimum of 3 years of experience in Pharmacovigilance with strong experience preferred in Pharmacovigilance Operations and/or PV affiliate OperationsStrong working knowledge of PV regulations and PV processesProficiency with standard desktop computing programs (e-mail, Word, Excel) and relational databases Experience of Oracle Argus Safety is preferredExcellent Project Management and interpersonal skills, results oriented and strong attention to detailAbility to manage multiple, complex projects in a fast-paced environment with capacity to prioritize, plan and organize work assignments under strict timelinesScholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.