Clinical Operations Manager

Scientific Search

Hybrid –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.
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 Apply
Lead complex trials across global regions with true operational authority
Hybrid role with high visibility and direct influence on clinical success
Work cross-functionally with Clinical Dev, DM, Stats, Safety & Regulatory
A culture that values rigor, collaboration, and decisive leadership
Competitive compensation + excellent benefits (details provided during interview)
What You’ll Be Doing
Oversee all operational aspects of assigned trials—start-up through close-out
Manage CRAs and IHCRAs; coach, review deliverables, ensure monitoring quality
Drive CRO oversight: KPIs, governance, performance management
Ensure TMF accuracy, inspection readiness, and documentation excellence
Lead RBM strategy, SDV/SDR optimization, and centralized monitoring activities
Support audits/inspections and act as escalation point for complex site issues
Monitor enrollment, deviations, CAPAs, and timeline risks
About You
8+ years clinical research + 6+ years on-site CRA experience
Strong oversight skills (in-house + CRO models)
Expert in GCP, RBM, and inspection readiness
Strong communicator, mentor, and cross-functional partner
How To Apply
Send your resume to View email address on click.appcast.io and reference Job #20167 .

Apply

Vacancy posted 16 hours ago

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