Lindus

Serve as an independent statistical expert on a Data and Safety Monitoring Board for an FDA-regulated mHealth study. Review interim analysis reports to provide evidence-based recommendations on study continuation or termination based on predefined stopping criteria.

Own the development strategy across the Lindus Therapeutics portfolio to reach value-generating proof-of-concept readouts efficiently. Lead a virtual organization of consultants and experts to manage regulatory, CMC, and clinical paths for in-licensed assets.

The role involves managing the end-to-end site lifecycle and monitoring for a major US-based clinical trial. You will also collaborate with product teams to help design and improve the Citrus trial monitoring platform.

Act as a clinical advisor for respiratory trials, providing expert input on protocol design, feasibility, and safety oversight. Support business development by lending scientific credibility to sponsor conversations and engaging with key opinion leaders.