Associate I/II, Regulatory Operations

Capricor Therapeutics(10 days ago)

San Diego, CAOnsiteFull TimeJunior$0 - $0Regulatory Affairs

About this role

Capricor Therapeutics is seeking an Associate I/II in Regulatory Operations to support regulatory document management, submission activities, and cross-functional collaboration in a biotech setting focused on cell and exosome-based therapies. The role involves ensuring compliance, maintaining documentation, and contributing to regulatory submissions and inspections.

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Required Skills

Regulatory Submissions
Document Management
eCTD
Veeva RIM
LORenz DocuBridge
Quality Checks
Regulatory Compliance
Microsoft Office
GxP Principles
Cross-functional Collaboration

About Capricor Therapeutics

capricor.com

Capricor Therapeutics, Inc. (NASDAQ: CAPR) is a San Diego–based biotechnology company developing cell- and exosome-based therapeutics for muscular and other select diseases. Its lead candidate, deramiocel (CAP‑1002), is an allogeneic cell therapy currently in Phase 3 clinical development for Duchenne muscular dystrophy. Capricor is also advancing exosome technology as a next‑generation platform, engineering exosomes to deliver nucleic acids and proteins to treat or prevent a variety of diseases. The company focuses on translating these platforms into novel therapeutic and preventive products.

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