Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Travere Therapeutics

Senior Director, Program Management

Travere Therapeutics

Senior Director leading program management at Travere Therapeutics for rare immune-mediated kidney diseases. Collaborating with cross-functional teams to drive integrated strategy from development to commercialization.

Posted 6/24/2026full-timeSan Diego • California • 🇺🇸 United StatesSenior💰 $219,000 - $285,000 per yearWebsite

About the role

Key responsibilities & impact
  • Lead cross-functional program planning and execution across clinical, regulatory, commercial, access, manufacturing, medical and nonclinical functions
  • Organize and lead strategy team meetings: set agendas, clarify objectives, document decisions, and proactively ensure accountability for action items
  • Develop and maintain integrated and often detailed development plans, timelines, budgets, and risk management frameworks
  • Identify critical path activities, interdependencies, and risks; proactively implement mitigation strategies
  • Coordinate program governance, including pro-active planning for decisions, identifying correct forum for decision making and leading the preparation of decision-ready materials
  • Partner with Program Lead and Alliance manager in managing alignment, communication and governance with our partner
  • Promote cross-functional alignment, transparency, and accountability to achieve development and commercialization milestones
  • Partner with Finance on program budgeting and forecasting; ensure alignment and manage process for executive endorsement
  • Contribute to departmental and corporate process improvements

Requirements

What you’ll need
  • Bachelor’s degree in Life Sciences or related field; Master’s preferred
  • 12+ years of relevant industry experience in biotech or pharmaceutical development
  • 5+ years of program or project leadership in complex drug development programs
  • Experience in rare disease / orphan drug / late-stage development desired
  • Understanding of regulatory requirements (NDA/MAA)
  • Demonstrated ability to lead and influence in a matrixed, cross-functional environment
  • Experience of working within a partnership, preferable with Asia based partner

Benefits

Comp & perks
  • Premium health, financial, work-life and well-being offerings for eligible employees and dependents
  • Wellness and employee support programs
  • Life insurance
  • Disability
  • Retirement plans with employer match
  • Generous paid time off

ATS Keywords

✓ Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
program planningrisk managementbudgetingforecastingproject leadershipdrug developmentregulatory requirementsdecision-makingprocess improvementstimeline management
Soft Skills
leadershipcommunicationaccountabilitycross-functional collaborationstrategic planninginfluencetransparencyorganizational skillsproactive problem-solvingteam management