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Clinical Operations Manager

  • Clinical Operations Manager job type Posted on: Oct 17, 2026
  • Clinical Operations Manager experience level Scientific Search
  • Clinical Operations Manager employment type Ewing, Kentucky
  • Clinical Operations Manager employment type Onsite
  • Clinical Operations Manager salary Full-time

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Job Title :

Clinical Operations Manager

Job Type :

Full-Time

Job Location :

Ewing Kentucky United States

Remote :

No

Jobcon Logo Job Description :

Job Description

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.\n
\n
\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
\n
Why You Should Apply

\n
    \n
  • Lead complex trials across global regions with true operational authority
  • \n
  • Hybrid role with high visibility and direct influence on clinical success
  • \n
  • Work cross-functionally with Clinical Dev, DM, Stats, Safety & Regulatory
  • \n
  • A culture that values rigor, collaboration, and decisive leadership
  • \n
  • Competitive compensation + excellent benefits (details provided during interview)

  • \n
What You’ll Be Doing

\n
    \n
  • Oversee all operational aspects of assigned trials—start-up through close-out
  • \n
  • Manage CRAs and IHCRAs; coach, review deliverables, ensure monitoring quality
  • \n
  • Drive CRO oversight: KPIs, governance, performance management
  • \n
  • Ensure TMF accuracy, inspection readiness, and documentation excellence
  • \n
  • Lead RBM strategy, SDV/SDR optimization, and centralized monitoring activities
  • \n
  • Support audits/inspections and act as escalation point for complex site issues
  • \n
  • Monitor enrollment, deviations, CAPAs, and timeline risks

  • \n
About You

\n
    \n
  • 8+ years clinical research + 6+ years on-site CRA experience
  • \n
  • Strong oversight skills (in-house + CRO models)
  • \n
  • Expert in GCP, RBM, and inspection readiness
  • \n
  • Strong communicator, mentor, and cross-functional partner

  • \n
How To Apply

Send your resume to and reference Job #20167.\n
\n

Jobcon Logo Position Details

Posted:

Oct 17, 2026

Reference Number:

466dd2a07a8d0fae

Employment:

Full-time

City:

Ewing

Job Origin:

ziprecruiter

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Aug 19, 2017 9am-6pm
All job seekers welcome!

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Job Description

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.\n
\n
\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
\n
Why You Should Apply

\n
    \n
  • Lead complex trials across global regions with true operational authority
  • \n
  • Hybrid role with high visibility and direct influence on clinical success
  • \n
  • Work cross-functionally with Clinical Dev, DM, Stats, Safety & Regulatory
  • \n
  • A culture that values rigor, collaboration, and decisive leadership
  • \n
  • Competitive compensation + excellent benefits (details provided during interview)

  • \n
What You’ll Be Doing

\n
    \n
  • Oversee all operational aspects of assigned trials—start-up through close-out
  • \n
  • Manage CRAs and IHCRAs; coach, review deliverables, ensure monitoring quality
  • \n
  • Drive CRO oversight: KPIs, governance, performance management
  • \n
  • Ensure TMF accuracy, inspection readiness, and documentation excellence
  • \n
  • Lead RBM strategy, SDV/SDR optimization, and centralized monitoring activities
  • \n
  • Support audits/inspections and act as escalation point for complex site issues
  • \n
  • Monitor enrollment, deviations, CAPAs, and timeline risks

  • \n
About You

\n
    \n
  • 8+ years clinical research + 6+ years on-site CRA experience
  • \n
  • Strong oversight skills (in-house + CRO models)
  • \n
  • Expert in GCP, RBM, and inspection readiness
  • \n
  • Strong communicator, mentor, and cross-functional partner

  • \n
How To Apply

Send your resume to and reference Job #20167.\n
\n

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