Associate Director, Clinical PM — Remote

Travere Therapeutics; New York (NY); On-site; USD 150,000 - 195,000; Full time

Benefits offered by this job

Premium health

Retirement plans with employer match

Generous paid time off

Job summary

Travere Therapeutics in San Diego (remote-friendly) seeks an Associate Director, Project Management to drive departmental timelines across Clinical Operations and Clinical Pharmacology. You will create integrated schedules, manage dependencies, and provide executives with clear milestones and risk insights.

With 8+ years in biotech/pharma and strong Smartsheet skills, you will influence cross-functional teams, ensure patient safety and compliance, and accelerate development programs while

Qualifications

• Bachelor's degree in life sciences, pharmacy, business, project management, or related discipline required; advanced degree preferred.
• 8+ years in biotech/pharma with 4+ years in project management for R&D or clinical development.
• Experience planning and managing complex multi-study timelines from strategy to execution.
• Direct PM experience supporting Clinical Operations; knowledge of Clinical Pharmacology preferred.
• Experience integrating functional timelines with broader program plans and governance milestones.
• PMI/PMP certification or equivalent training preferred.

Responsibilities

• Own and maintain departmental timelines for Clinical Operations and Clinical Pharmacology across studies.
• Build scalable Smartsheet solutions with integrated schedules, dependencies, dashboards, and reports.
• Translate strategies into executable plans with clear activities and critical-path visibility.
• Coordinate functional plans into integrated program timelines with governance alignment.
• Integrate milestones across study start-up, activation, enrollment, data review, and reporting.
• Collaborate cross-functionally to map interdependencies and build end-to-end timelines.
• Identify bottlenecks, plan scenarios, and drive acceleration options with clear decisions.
• Lead timeline reviews, ensure accountability, and document action records.
• Maintain integrated risk, issue, action, and decision tracking with impact assessments.
• Provide dashboards and status updates to leaders, governance teams, and executives.
• Support regulatory planning and submissions by reflecting activities in the integrated plan.
• Coordinate timelines with CROs, labs, vendors, and external partners.

Skills

Advanced Smartsheet capability

Project management

Executive communication

Facilitation

Influencing skills

Attention to detail

Cross-functional collaboration

Risk management

Education

Bachelor's degree in life sciences, pharmacy, business, project management, or related discipline

Advanced degree preferred

PMP certification preferred

Tools

Microsoft Project

Excel

PowerPoint

Teams

SharePoint

Document-management systems

Job description

Travere Therapeutics in San Diego (remote-friendly) seeks an Associate Director, Project Management to drive departmental timelines across Clinical Operations and Clinical Pharmacology. You will create integrated schedules, manage dependencies, and provide executives with clear milestones and risk insights.

With 8+ years in biotech/pharma and strong Smartsheet skills, you will influence cross-functional teams, ensure patient safety and compliance, and accelerate development programs while