Jobs at Attovia Therapeutics

Leads CMC regulatory strategy, submissions, compliance, and manufacturing activities for a biologics pipeline. The role authors CMC filing sections, interprets FDA/EMA and ICH requirements, manages regulatory correspondence, and provides technical guidance to external CDMOs on process development, analytical methods, formulation, manufacturing, and clinical supply. It collaborates with Quality, Regulatory Affairs, Portfolio Management, consultants, and vendors to coordinate development milestones, manufacturing transitions, and commercial CMC strategy.

Leads investor relations strategy for a clinical-stage biopharmaceutical company, managing investor and analyst relationships, earnings communications, roadshows, presentations, disclosure compliance, market analysis, and IR infrastructure. Also serves as Executive Team Chief of Staff, supporting the CEO and executive committee with meeting coordination, decision follow-up, communications, special projects, and cross-functional initiatives.