Clinical Operations ManagerHybrid – Pennington, NJ (Travel Required)Are you a clinical operations pro who thrives at the intersection of strategy, oversight, and hands-on leadership? My client—a fast-growing biopharma advancing meaningful global studies—is searching for a Clinical Operations Manager who can elevate trial execution, sharpen CRO performance, and mentor CRAs while keeping every study inspection-ready.This is your chance to lead high-impact trials across in-house and outsourced models, shape monitoring strategy, and ensure quality that stands up to global regulatory scrutiny.Why You Should ApplyLead complex trials across global regions with true operational authorityHybrid role with high visibility and direct influence on clinical successWork cross-functionally with Clinical Dev, DM, Stats, Safety & RegulatoryA culture that values rigor, collaboration, and decisive leadershipCompetitive compensation + excellent benefits (details provided during interview)What You’ll Be DoingOversee all operational aspects of assigned trials—start-up through close-outManage CRAs and IHCRAs; coach, review deliverables, ensure monitoring qualityDrive CRO oversight: KPIs, governance, performance managementEnsure TMF accuracy, inspection readiness, and documentation excellenceLead RBM strategy, SDV/SDR optimization, and centralized monitoring activitiesSupport audits/inspections and act as escalation point for complex site issuesMonitor enrollment, deviations, CAPAs, and timeline risksAbout You8+ years clinical research + 6+ years on-site CRA experienceStrong oversight skills (in-house + CRO models)Expert in GCP, RBM, and inspection readinessStrong communicator, mentor, and cross-functional partnerHow to ApplySend your resume to victoria@scientificsearch.com and reference Job #19801. #LI-VL1Type: Direct HireCategory: BiopharmaDate Posted: 2026-03-24