Hybrid –Ewing Area , NJ (Travel Required)
Have you got the right qualifications and skills for this job Find out below, and hit apply to be considered.
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
Send your resume to and reference Job #20167 .
Have you got the right qualifications and skills for this job Find out below, and hit apply to be considered.
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)
- 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
- 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
Send your resume to and reference Job #20167 .
Clinical Operations Manager in trenton at Unknown Company
This position is listed as full time and hybrid.