Senior Manager, Regulatory Affairs Project Management
Travere Therapeutics(1 month ago)
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.
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
About Travere Therapeutics
travere.comTravere 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 →Apply instantly with AI
Let ApplyBlast auto-apply to jobs like this for you. Save hours on applications and land your dream job faster.
More jobs at Travere Therapeutics
Senior Medical Science Liaison (Mid-Atlantic North)
Travere Therapeutics(4 days ago)
Clinical Account Manager (Boston, MA)
Travere Therapeutics(7 days ago)
Associate Director, Patient Support Services
Travere Therapeutics(12 days ago)
Senior Director, Digital Innovation and Strategy – Commercialization
Travere Therapeutics(14 days ago)
Similar Jobs
Submission Manager, Regulatory Operations
Crinetics Pharmaceuticals(12 days ago)
Submission Content Manager, Regulatory Affairs Operations
Olema Oncology(11 days ago)
Associate I/II, Regulatory Operations
Capricor Therapeutics(19 days ago)
Manager, CMC Regulatory Affairs
Capricor Therapeutics(19 days ago)
Manager, Regulatory, EU (1 year contract)
BridgeBio Pharma(2 months ago)
Associate - Regulatory Affairs (Publishing)
ClinChoice(6 days ago)