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Associate Director, Vendor & Relationship Management

Job in San Diego, San Diego County, California, 92189, USA
Listing for: Scorpion Therapeutics
Part Time position
Listed on 2026-08-30
Job specializations:
  • Business
    Regulatory Compliance Specialist, Operations Management
Salary/Wage Range or Industry Benchmark: 140000 - 190000 USD Yearly USD 140000.00 190000.00 YEAR
Job Description & How to Apply Below

Position Summary

Associate Director, Vendor & Relationship Management (hybrid; office 3 days/week; based in Princeton, NJ or San Diego, CA).

Primary Responsibilities
  • Develop and execute vendor/supplier relationship management strategies; manage critical partners (CROs, labs, functional service providers, clinical technologies, patient recruitment/retention).
  • Serve as primary point of contact for vendor operational issues; resolve and escal
    * ate via governance pathways.
  • Facilitate vendor governance (operational/steering committee meetings).
  • Build and maintain supplier scorecards, dashboards, and KPIs to monitor performance, risks, and trends.
  • Run routine business reviews with vendors (partnering with Sourcing and Legal as needed).
  • Oversee vendor performance for outsourced clinical trials with Clinical Operations; ensure alignment to timelines, budgets, and quality.
  • Partner with cross-functional teams to support timely, compliant delivery of services.
  • Support inspection readiness (audits, oversight documentation, CAPA with Quality).
  • Map processes and implement standardized vendor oversight practices.
  • Drive continuous improvement: performance, efficiency, collaboration, innovation, best practices/tools, and cost/demand optimization.
  • Support vendor reporting/dashboards, analyze metrics, mentor stakeholders, influence cross-functionally.
Education/Experience/Skills (Required/Preferred)
  • BS in life science/related field; advanced degree preferred. ~8 years in clinical trial operations, vendor/CRO oversight, or supplier relationship management (or equivalent).
  • Strong clinical trial operations knowledge; working knowledge of ICH GCP, regulatory and quality expectations for outsourced activities.
  • Analytical skills (scorecards/KPIs/dashboards); experience with R&D outsourcing/vendor governance; financial exposure (budgeting/accruals).
  • Experience with audits/inspection readiness; familiarity with partnership management; excellent communication/organization.
  • Travel domestically/internationally.
Benefits
  • Competitive base + discretionary bonus and equity awards; medical/dental/vision; employer-paid life/disability/travel/EAP; 401(k) match; ESPP; 15+ vacation days; 13-15 paid holidays; paid sick time; paid parental leave; tuition assistance.
(If applicable) Physical/Work Requirements
  • Ability to work standard office and independently from remote locations; occasional lifting/moving up to 20 lbs; travel overnight and/or work after hours as needed.
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Position Requirements
10+ Years work experience
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