Clinical Operations Manager in Ewing

Job DescriptionHybrid –Ewing Area , NJ (Travel Required)

Area 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.\n
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\nThis 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.\n
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Why You Should Apply

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• Lead complex trials across global regions with true operational authority

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• Hybrid role with high visibility and direct influence on clinical success

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• Work cross-functionally with Clinical Dev, DM, Stats, Safety & Regulatory

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• A culture that values rigor, collaboration, and decisive leadership

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• Competitive compensation + excellent benefits (details provided during interview)

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What You’ll Be Doing

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• Oversee all operational aspects of assigned trials—start-up through close-out

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• Manage CRAs and IHCRAs; coach, review deliverables, ensure monitoring quality

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• Drive CRO oversight: KPIs, governance, performance management

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• Ensure TMF accuracy, inspection readiness, and documentation excellence

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• Lead RBM strategy, SDV/SDR optimization, and centralized monitoring activities

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• Support audits/inspections and act as escalation point for complex site issues

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• Monitor enrollment, deviations, CAPAs, and timeline risks

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About You

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• 8+ years clinical research + 6+ years on-site CRA experience

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• Strong oversight skills (in-house + CRO models)

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• Expert in GCP, RBM, and inspection readiness

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• Strong communicator, mentor, and cross-functional partner

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How To Apply

Send your resume to Emily@scientificsearch.com and reference Job #20167.\n
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