Senior Regulatory Project Manager

Travere Therapeutics; Manchester (NH); Hybrid; USD 150,000 - 195,000; Full time

Job summary

Travere Therapeutics is seeking an Associate Director, Regulatory Project Manager to lead and coordinate global regulatory activities ensuring health authority compliance. The role supports submissions for investigational and commercial therapies and drives cross‑functional collaboration to meet timelines.

You will partner with Regulatory Strategy leaders to create project timelines, dashboards, and meeting schedules, while mentoring the PM team and aligning with program goals.

Qualifications

• 8+ years of Project Management experience in Biotech or Pharmaceutical industry.
• PMP certification strongly preferred.
• Expertise with timeline development and management software.

Responsibilities

• Lead regulatory project management activities for global development programs, ensuring timelines and submission deliverables align with strategy.
• Coordinate Global Regulatory Team meetings, agenda planning, and action tracking.
• Develop and maintain integrated regulatory project timelines reflecting health authority milestones and cross-functional dependencies.
• Oversee planning and tracking of major submissions and maintenance activities (INDs, NDAs, BLAs, supplements, annual reports, DSURs).
• Collaborate with Regulatory Operations, Clinical Development, and other functions to ensure timely, high-quality deliverables.
• Create and maintain regulatory dashboards, milestone trackers, and status reports for leadership and program teams.

Skills

Project management

Cross-functional collaboration

Communication

Problem solving

Education

Bachelor's degree in Life Sciences or related discipline

MS, Pharm D, PhD preferred

PMP certification strongly preferred

Tools

Smartsheets

MS Project

Job description

Travere Therapeutics is seeking an Associate Director, Regulatory Project Manager to lead and coordinate global regulatory activities ensuring health authority compliance. The role supports submissions for investigational and commercial therapies and drives cross‑functional collaboration to meet timelines.

You will partner with Regulatory Strategy leaders to create project timelines, dashboards, and meeting schedules, while mentoring the PM team and aligning with program goals.