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 Intern will develop software tools for R&D, design applications for scientific data handling, and support computational pipelines, with a strong focus on collaboration in a biotech setting.

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

Execute and develop high-throughput Illumina and Oxford Nanopore NGS workflows including library prep, sample QC, and sequencing. Extract DNA/RNA, assist with data analysis and study reports, maintain electronic lab notebooks, and present results to cross-functional teams. Work independently on experiments and support development of sequencing pipelines.

Execute mRNA production and purification development for GMP-relevant processes, develop analytical assays, support enzymatic reaction and chromatographic/filtration scale-up, produce materials for formulation and discovery, and run process improvement studies.

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.