Senior Director, Program Management

Travere Therapeutics; Providence (RI); On-site; USD 219,000 - 285,000; Full time

Benefits offered by this job

Comprehensive health benefits

Retirement plans with employer match

Generous paid time off

Job summary

Travere Therapeutics is seeking a Senior Director of Program Management to spearhead their development program in rare immune-mediated kidney diseases. This leadership role requires extensive experience in managing complex drug development programs, coordinating cross-functional teams, and ensuring alignment with strategic goals.

The ideal candidate will have over 12 years in biotech, with a strong foundation in regulatory processes and exceptional organizational skills. This position is based in Providence, Rhode Island, and emphasizes partnership, communication, and accountability across teams.

Qualifications

• 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.

Responsibilities

• Lead cross-functional program planning and execution across various functions.
• Develop and maintain integrated development plans, timelines, and budgets.
• Coordinate program governance and decision-making processes.

Skills

Cross-functional leadership

Strategic planning

Project management

Communication skills

Organizational skills

Education

Bachelor's degree in Life Sciences or related field

Tools

Word

Excel

PowerPoint

Smartsheet

Job description

Position Summary

The Senior Director, Program Management will be the program management lead for Travere's development program in rare immune‑mediated kidney diseases and may support Travere programs, corporate initiatives, or additional products that may be added to Travere Therapeutics development portfolio. This role partners closely with the Program Lead and cross‑functional Strategy Team to drive integrated strategy, planning execution, governance, and decision‑making across the full product lifecycle—from development through commercialization. This role will also partner with Alliance Management in managing alignment, communication and governance with our partner.

The ideal candidate excels in complex cross‑functional environments, and has a proven ability to structure program plans, align stakeholders, and drive high‑quality decisions within the rare disease environment. Prior experience managing partnered programs, particularly with Asia‑based partners is preferred.

Key Responsibilities

• 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.

Skills and Qualifications

• Bachelor's degree in Life Sciences or related field; Master's preferred. Equivalent combination of education and applicable job experience may be considered.
• 12+ years of relevant industry experience in biotech or pharmaceutical development.
• 5+ years of program or project leadership in complex drug development programs, including proficiency in strategic planning.
• Experience in rare disease / orphan drug / late‑stage development desired.
• Understanding of regulatory requirements (NDA/MAA) and support of regulatory submissions.
• Demonstrated ability to lead and influence in a matrixed, cross‑functional environment.
• Experience of working within a partnership, preferable with Asia based partner.

Additional Skills/Experience/Requirements

• The ideal candidate will embody Travere's core values: Courage, Community Spirit, Patient Focus and Teamwork.
• Exceptional organizational skills, including proficiency in Word, Excel, PowerPoint and Smartsheet. Basic understanding of use of ChatGPT to deliver efficiencies.
• Proven ability to develop and manage complex project plans, timelines, budgets, and critical path is required.
• Strong facilitation skills and ability to drive structured, decision‑focused meetings.
• Must have demonstrated successful ability to manage and drive cross‑functional working teams within product development internationally.
• Proven ability in negotiating and gaining consensus in a matrixed and global organization.
• Must possess excellent prioritization, resource planning, and communication skills, with the ability to translate complex information for diverse stakeholders.
• Organizational agility and adaptability in a dynamic environment.
• All positions have an essential job function to be able to perform face to face work with colleagues and/or onsite in San Diego as requested. No role is expected to be 100% remote.

Total Rewards Offerings

Travere provides comprehensive total rewards offerings that demonstrate our commitment as a diverse, equitable, people‑centric, and pay‑for‑performance organization.

Benefits

Our benefits include 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 and generous paid time off.

Compensation

Our competitive compensation package includes a combination of both cash compensation (base pay and short‑term incentive) and long‑term incentive compensation (company stock), designed to recognize, retain, and reward employees.

Target Base Pay Range

$219,000.00 – $285,000.00

*This information is current as of the date of this posting and may be modified in the future. Actual pay offered to a candidate will depend on a variety of factors including the candidate's experience, education, skills, and location.

Travere Therapeutics, Inc. is an EEO/AA/Veteran/Disability Employer.