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Associate Director PMO, Clinical Programs

Job in Irvine, Orange County, California, 92713, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-09-12
Job specializations:
  • Business
Salary/Wage Range or Industry Benchmark: 180000 - 240000 USD Yearly USD 180000.00 240000.00 YEAR
Job Description & How to Apply Below

Duties & Responsibilities:

  • Own the enterprise Integrated Clinical Portfolio Roadmap by consolidating function-owned study plans/forecasts into an integrated, forward-looking view aligned to product, regulatory, supply, launches, lifecycle priorities, and post-market evidence commitments.
  • Lead Supply and Demand Integration: convert study plans/enrollment/site activation into time-phased demand for equipment, investigational products, components, and ancillary materials; maintain rolling forecasts and reconcile against inventory, capacity, lead times, labeling, country requirements, and budget constraints.
  • Own enterprise governance cadence/decision support via portfolio analytics, scenario planning, prioritization, documentation of decisions/decision rights, and action tracking to closure.
  • Own cross-functional RAID and readiness: integrated view of risks/issues/dependencies/constraints affecting multiple functions/programs; facilitate resolution and upscale portfolio-level blockers through governance.
  • Own portfolio analytics/KPIs/financial visibility and consolidated reporting to recommend prioritization and scenario decisions.
  • Lead resource and scenario planning (demand/capacity trade-offs) and recommend sequencing/mitigation when milestones are at risk.
  • Serve as central PMO coordination point across Scientific Affairs, R&D, Regulatory, Quality, Supply Chain, Commercial, Finance, regions, and program leadership.
  • Drive PMO maturity and continuous improvement; coach partners on integrated planning and escalation quality.
Qualifications:
  • Bachelor’s degree in Life Sciences/Engineering or related field (required); MS/MPH/MBA/PhD preferred.
  • 10+ years in clinical program/portfolio management (Med Tech, devices, diagnostics, or life sciences).
  • Strong clinical study design, regulatory, and product development knowledge; experience managing cross-functional clinical portfolios tied to launches/lifecycle.
  • Familiarity with PMO governance/portfolio frameworks; proficient with Smartsheet/Power BI/Wrike/Microsoft Project.
Required/Preferred

Skills:
  • PMP/PgMP/MSP preferred;
    Lean Six Sigma or Agile a plus.
  • Strategic integrator; strong analytical/prioritization/resource management; influential communicator; data-driven, collaborative leader.
  • Preferred skills (examples):
    Agility Jumps, Business Alignment, Collaboration, Continuous Improvement, Mentorship, Operational Excellence, Organizing, Performance Measurement, Process Control, PMM, PMO, Project Reporting/Schedule, Quality Control, Research & Development, Technical Credibility.
Additional

Position Requirements :
  • Travel up to 25% (domestic/international).
Benefits (explicitly stated):
  • Vacation 120 hrs/year;
    Sick time 40 hrs/year (CO 48, WA 56);
    Holiday pay incl. Floating Holidays 13 days/year;
    Work/Personal/Family time up to 40 hrs/year;
    Parental leave 480 hrs;
    Bereavement 240 hrs (immediate) / 40 hrs (extended);
    Caregiver leave 80 hrs (52-week rolling);
    Volunteer leave 32 hrs;
    Military Spouse Time-Off 80 hrs/year.
Position Requirements
10+ Years work experience
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