Teams at Sarepta Therapeutics

Support planning, execution, and management of clinical trials by maintaining inspection-ready Trial Master File (TMF), coordinating clinical documents, supplies, and drug shipments, performing TMF quality checks, liaising with sites and vendors, supporting contracts/invoices, assisting meetings and timelines, and supporting cross-functional trial activities. Remote role with ~10% travel.

Lead pharmacovigilance (GVP) quality oversight and audit program; design and execute audit strategy; manage audit reports, CAPA, and remediation; support inspection readiness and regulatory interactions; review SOPs and QMS elements; collaborate cross-functionally to identify risks and ensure sustainable compliance.

Lead commercial reporting and operations for Commercial organization: build and maintain dashboards and Executive reports, manage contracted analysts, administer Tableau, partner with cross-functional teams (Sales Effectiveness, Patient Services, Data Management, Site Readiness), set reporting standards, manage delivery schedules, and support Veeva/CRM alignment and data stewardship.