Director of Clinical Operations

Director of Clinical Operations ABOUT THE ROLEWe are partnering with a growing clinical research site in the Bronx to recruit a Senior Director of Clinical Operations "” the operational beast who will own site performance end-to-end.This is the go-to person who runs the site. Trial activation timelines, enrollment performance, study quality, regulatory compliance, financial operations, and the coordinator and research nursing teams all roll up to this seat. The right candidate has lived this work at a research site or site network before "” they already know what good looks like, what breaks, and how to fix it without a 90-day diagnostic.This is an onsite role in the Bronx. Five days a week, in the building with the team, the patients, the PIs, and the studies. The site needs presence and operational leadership in the room.WHAT YOU'LL OWNEnd-to-end site performance: trial activation timelines, enrollment to target, retention, data quality, regulatory compliance, and financial outcomes per studyDirect leadership of clinical operations staff, including CRCs, research nurses, regulatory and data coordinators, and operations supportOperational accountability across the full study lifecycle: feasibility input, site activation, enrollment ramp, conduct, monitoring response, database lock, and close-outSponsor and CRO relationships at the operational level "” site qualification visits, monitoring visits, audit response, and corrective action planningStandardization of SOPs, training programs, quality systems, and operational metrics across the siteBudget management at the study level: per-protocol P&L oversight, invoicing accuracy, and study-level margin disciplineHiring, onboarding, performance management, and retention of clinical operations staffDirect partnership with site leadership and PIs on prioritization, capacity planning, and study mix decisionsWHAT WE'RE LOOKING FORRequired10+ years of clinical research operations experience, with at least 5 years in a senior operational role at a clinical research site, multi-site network, SMO, or IRODemonstrated track record of owning site performance metrics "” enrollment, retention, activation timelines, quality, and study-level financialsDirect experience managing CRC, research RN, regulatory, and data coordination teamsDeep working knowledge of GCP, FDA regulations, sponsor and CRO operational expectations, and audit readinessStrong financial acumen at the study level "” feasibility budgeting, invoicing, monitoring of study P&LExperience standing up or scaling SOPs, training programs, and operational quality systems at a siteBachelor's degree required; advanced degree, RN/BSN, or relevant certification (CCRC, CCRP, ACRP-CP) preferredStrongly PreferredVP or Director-level experience at a comparable research site network or SMOTrack record running multi-therapeutic-area sites with diverse sponsor and CRO portfoliosPrior experience in fast-growing or PE-backed clinical research environmentsHands-on experience with CTMS, eRegulatory, EDC, and patient recruitment platformsNon-NegotiablesOnsite five days a week in the Bronx. This is not a hybrid or remote role.Site-side or site-network operational experience. Pure CRO operations, pharma operations, or academic medical center operations backgrounds will not fit this role.A demonstrated bias toward operational ownership and execution "” this is a doer's seat, not a strategist's seat.

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