Senior Clinical Operations Leader - Global Trials (Remote)

Travere Therapeutics; Manchester (NH); On-site; USD 132,000 - 172,000; Full time

Benefits offered by this job

Premium health benefits

Work-life and well-being offerings

Company stock

Job summary

Travere Therapeutics is seeking a Senior Manager, Clinical Operations in San Diego to supervise Phase 1–3 trials, coordinate internal teams and CROs, and ensure study execution on time and within budgets.

The ideal candidate has 7+ years in clinical trials and 2+ years leading studies for sponsors or CROs, with strong regulatory knowledge and proficiency in MS Office, MS Project, Smartsheet, IRT, and eTMF. Travel 10–20% is required.

Qualifications

• Bachelor's degree or equivalent combination of education and experience.
• 7+ years of clinical trial experience required with 2+ years in leading studies for sponsor or CRO.
• Experience with global regulatory and compliance for clinical research (US CFR, EU CTD, ICH E6).
• Phase 1–3 study experience or international studies preferred.

Responsibilities

• Oversee daily operations of internal study teams, CROs, sites and vendors for trials.
• Triage, resolve, or escalate study issues to management and ensure timelines.
• Manage study programs, budgets, SMTs and on-time milestone delivery.
• Coordinate with Biometrics, PV, and others to ensure compliant study execution.
• Develop study documents and budgets; monitor regulatory docs and site startup.
• Lead cross-functional activities and communicate key updates to stakeholders.

Skills

Cross-functional leadership

Project management

MS Office

MS Project

Smartsheet

IRT

eTMF

Clinical systems knowledge

Communication skills

Budget management

Education

Bachelor's degree

Tools

MS Office

MS Project

Smartsheet

IRT

eTMF

Job description

Travere Therapeutics is seeking a Senior Manager, Clinical Operations in San Diego to supervise Phase 1–3 trials, coordinate internal teams and CROs, and ensure study execution on time and within budgets.

The ideal candidate has 7+ years in clinical trials and 2+ years leading studies for sponsors or CROs, with strong regulatory knowledge and proficiency in MS Office, MS Project, Smartsheet, IRT, and eTMF. Travel 10–20% is required.