Support scale-up and production of lipid nanoparticles (LNPs) with nucleic acid payloads by executing mixing and downstream purification experiments, developing robust formulations, enabling tech-transfer and stability, characterizing LNPs, and coordinating cross-functional process development activities.

Lead clinical trial operations for Strand's clinical and preclinical programs, managing budgets, timelines, CROs, vendor oversight, regulatory interactions, QA/inspection readiness, site strategy, and a clinical operations team to ensure compliant, high-quality trial execution.

The Vice President of Regulatory Sciences will lead regulatory efforts, manage strategies for clinical and preclinical assets, and interact with regulatory agencies.

The Director of Contracts leads complex biotech agreements and manages risk governance, contracting strategy, and legal operations within a clinical stage biotechnology setting.