Kriya Therapeutics, Inc. Benefits Overview

Provide scientific leadership across clinical study lifecycle including protocol and regulatory document development, study design support, data review and analysis, vendor and investigator selection oversight, training, and preparation of abstracts, manuscripts, and clinical study reports to ensure scientific quality and compliance.

The Associate Director leads CMC regulatory efforts, ensuring compliance with global regulations, managing submissions, and providing strategic regulatory guidance.

The Vice President, Pharmacovigilance oversees safety surveillance programs, evaluates adverse events, ensures regulatory compliance, and collaborates with teams on risk management strategies.