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Senior Manager, Alliance Program Management

Job in Indianapolis, Hamilton County, Indiana, 46262, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-08-30
Job specializations:
  • Management
    Operations Management, Project & Program Management, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 110000 - 170000 USD Yearly USD 110000.00 170000.00 YEAR
Job Description & How to Apply Below
Location: Indianapolis

Senior Manager, Alliance Program Management Job Responsibilities

  • Serve as the primary point of contact and operational liaison for assigned external alliances and partnerships.
  • Build and maintain strong, productive relationships with partner organizations at all levels.
  • Facilitate joint governance meetings, steering committees, and operational reviews with alliance partners.
  • Drive alignment on program objectives, timelines, deliverables, and performance expectations.
  • Ensure compliance with alliance agreements, contracts, and collaboration frameworks.
  • Monitor partner performance against contractual obligations and KPIs.
  • Lead cross-functional teams across internal functions (Manufacturing, Quality, Regulatory, Finance, Legal) and external partners to deliver program goals.
  • Develop and maintain integrated program plans, timelines, and resource allocation across multiple concurrent alliances and geographically distributed teams.
  • Ensure all program activities are executed on time, within scope, and within budget.
  • Bridge site operations teams and global program leadership to align local execution with enterprise priorities.
  • Apply AI to improve team execution and decision-making.
  • Prepare program status reports and executive-level updates.
  • Translate complex technical and operational information for stakeholders.
  • Foster transparency and open communication across alliance interfaces.
Required Qualifications
  • Bachelor's degree in Chemistry, Chemical Engineering, Biochemistry, Pharmaceutical Sciences, Nuclear Chemistry, Radiochemistry, or related; M.S. or Ph.D. strongly preferred.
  • 8+ years in pharmaceutical/biopharmaceutical industry; at least 5 years in process development and/or manufacturing (small molecule and/or RPT a plus).
  • Deep understanding of process development, API manufacturing, tech transfer, CMC, and GMP manufacturing; radiopharmaceutical manufacturing principles, isotope logistics, and RPT regulatory frameworks a plus.
  • Demonstrated experience managing complex, multi-stakeholder, multi-site programs; PMP a plus.
  • Prior alliance/partner management (CDMOs/strategic alliances preferred).
  • Experience operating in matrix organizations across site and global teams.
Benefits (explicitly listed)
  • Health coverage (medical, pharmacy, dental, vision).
  • Wellbeing support programs.
  • Financial wellbeing/protection (401(k), disability, life insurance, etc.).
  • Paid time off (including flexible time off or 160 hours paid vacation depending on location/role type).
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Position Requirements
10+ Years work experience
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