Associate Director PMO, Clinical Programs
Job in
Irvine, Orange County, California, 92713, USA
Listed on 2026-09-12
Listing for:
Scorpion Therapeutics
Full Time
position Listed on 2026-09-12
Job specializations:
-
Business
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.
- 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.
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.
Position Requirements :
- Travel up to 25% (domestic/international).
- 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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