Zachary F.

I help preclinical and clinical research teams move projects forward when timelines are tight and requirements are evolving. My background combines hands-on biomedical research experience with clinical study operations support, vendor coordination, and documentation management. Recently, I have been working with an early-stage medical device company to obtain quotes for experimental services, interpret scientific requirements, and coordinate across vendor teams to deliver results under fast timelines. I am comfortable translating complex scientific needs into clear, actionable plans so founders and scientists can focus on strategy while projects stay organized. I can assist with: • Vendor sourcing and quote coordination for lab and clinical services • Reviewing technical requirements (gene panels, assay methods, biospecimen workflows) • SOP and protocol drafting or cleanup • Clinical study sample tracking and data organization • Cross-functional coordination and follow-up • Documentation and record keeping Technical areas I can support include: • Flow cytometry data review and interpretation • Assay and protocol review • Biospecimen workflow design • Scientific literature review • Data validation and reporting Before consulting, I supported Phase 2 clinical study operations at a clinical biopharma company by tracking biospecimens, coordinating vendors, maintaining compliant documentation, and helping teams stay organized during fast-moving projects. Clients value my persistence, attention to detail, and calm approach under ambiguity. If your project needs steady operational support so your team can focus on science and strategy, I’d be glad to help.