Travere Therapeutics

Senior Manager, Regulatory Affairs Project Management

Travere Therapeutics(1 month ago)

St. Gallen, Switzerland, Switzerland, Rapperswil-Jona, SwitzerlandOnsiteFull TimeSenior$126,597 - $171,511 (estimated)Regulatory - TTSG
Apply Now

About this role

The Regulatory Project Manager (RPM) manages end-to-end EU and Rest of World regulatory activities for Travere Therapeutics, coordinating internal and external partners to ensure timely regional health authority submissions across product lifecycles. The role owns the Smartsheet submission ecosystem, tracks country-specific dossier adaptations and approval timelines, and delivers executive-ready status reporting. Located in Rapperswil-Jona, the RPM supports cross-functional alignment and continuous improvement of regulatory project processes.

View Original Listing

Required Skills

  • Project Management
  • Regulatory Submissions
  • Timeline Management
  • Smartsheet
  • MS Project
  • eCTD
  • Veeva RIM
  • Stakeholder Communication
  • Executive Presentations
  • Document Control

+1 more

Qualifications

  • Bachelor's Degree in Life Sciences
  • MS
  • PharmD
  • PhD
  • PMP Certification
Travere Therapeutics

About Travere Therapeutics

travere.com

Travere Therapeutics is a biopharmaceutical company whose mission is to identify, develop and deliver life-changing therapies to people living with rare disease.

View more jobs at Travere Therapeutics

ApplyBlast uses AI to match you with the right jobs, tailor your resume and cover letter, and apply automatically so you can land your dream job faster.

© All Rights Reserved. ApplyBlast.com