Los Angeles, CA7 days ago
You will own study launch and control across active diagnostic studies, including: translating protocol and scope into a real execution plan; identifying and activating the right sites; making sure site qualification and startup files are complete; driving SIV readiness; coordinating kits, sample logistics, lab workflows, EDC, monitoring, and data needs; making sure Salesforce, trackers, and project tools reflect reality; identifying timeline, scope, budget, and client-commitment risks early; escalating issues before they become fire drills; keeping client-facing deliverables moving; making sure project status is evidence-backed, not just verbally reported. We are looking for someone who: has run multiple studies from pre-submission through closeout; has the individual expertise and experience to do the underlying work themselves, and the judgment to know when to delegate versus step in directly; can manage across clinical, lab, data, site, vendor, and client workflows; can quickly identify what data matters and what does not; makes project reality visible before it becomes a problem; has experience working in or managing a clinical lab, which is a strong plus.