Global Regulatory Project Lead — Remote

Travere Therapeutics; Washington (District of Columbia); On-site; USD 150,000 - 195,000; Full time

Job summary

Travere Therapeutics is seeking an Associate Director, Regulatory Project Manager to lead global regulatory activities for rare disease therapies. You will coordinate cross-functional teams, manage timelines, and drive submission readiness while ensuring compliance with health authority requirements.

The role requires 8+ years in biotech/pharma PM, PMP preferred, and experience with Smartsheets/MS Project. This position is remote from the USA with some domestic/international travel, reporting

Qualifications

• 8+ years of Project Management experience in Biotech or Pharmaceutical industry.
• Regulatory specific project management experience preferred.
• PMP certification is strongly preferred.
• Expertise with timeline development and management software (Smartsheets, MS Project).

Responsibilities

• Lead regulatory project management activities for global development programs.
• Drive Global Regulatory Team meetings: agenda, decisions, follow-up actions.
• Develop and maintain integrated regulatory timelines reflecting milestones.
• Oversee submissions and maintenance activities (INDs, NDAs, BLAs, etc.).
• Collaborate across Regulatory Ops, Clinical, CMC, Biostatistics, Quality, and partners to ensure timely deliverables.
• Support health authority interactions, advisory committees, and inspection readiness.

Skills

Project management

Regulatory knowledge

Cross-functional collaboration

Communication

Leadership

Education

Bachelor's degree in Life Sciences

MS/PhD preferred

Tools

Smartsheets

MS Project

Job description

Travere Therapeutics is seeking an Associate Director, Regulatory Project Manager to lead global regulatory activities for rare disease therapies. You will coordinate cross-functional teams, manage timelines, and drive submission readiness while ensuring compliance with health authority requirements.

The role requires 8+ years in biotech/pharma PM, PMP preferred, and experience with Smartsheets/MS Project. This position is remote from the USA with some domestic/international travel, reporting