Teams at Entrada Therapeutics

Provide Tier 2 end-user and lab IT support for desktops, laptops, mobile devices, and scientific instruments. Support Windows/macOS, Microsoft 365 and collaboration tools; manage onboarding/offboarding, asset inventory, patching, endpoint management, and backups. Deploy and maintain lab systems (ELN, LIMS, CDS, Chromeleon, SDMS, instrument PCs), ensure integrations, follow change management/validation, coordinate vendors, and drive automation and process improvements in a compliant life sciences environment.

Leads and supports global clinical trial start-up and enrollment activities, including regulatory submissions, country and site selection, budgets, site activation, informed consent review, document collection, protocol amendments, CRO and vendor oversight, issue resolution, and study-specific training. Ensures deliverables meet timelines and comply with ICH, GCP, local regulations, and company procedures. This is a part-time, long-term remote contract role requiring approximately 10% travel.

Lead and support statistical strategy for clinical trials, author SAPs and regulatory documents, oversee outsourced CRO biostatistics deliverables (TFLs), review randomization procedures, and manage vendor relationships. Part-time long-term contract (~20-25 hours/week) supporting rare-disease programs and regulatory submissions.