Remote Director, Pharmaceutical Compliance

Mineralys Therapeutics, Inc.; Northern (KY); Hybrid; USD 220,000 - 235,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401K plan

Time off

Job summary

Mineralys Therapeutics, Inc. is seeking a Director, Compliance to lead the company’s global compliance program. The role reports to the Vice President, Compliance and drives policy development, training, and monitoring across high‑risk activities.

The ideal candidate has extensive pharmaceutical compliance experience, including HCP engagement, FMV processes, and investigations, with a track record of timely program improvements and collaboration across functions.

Qualifications

• 12+ years of compliance or compliance operations experience in the pharmaceutical industry.
• Experience building or significantly enhancing a pharmaceutical compliance program, including policy development, training, monitoring, and investigations.
• Experience with HCP engagement programs, FMV processes, and professional services agreement compliance.
• Experience with compliance risk assessment methodologies and monitoring program design and execution.

Responsibilities

• Build, refine, and mature a best-in-class compliance program aligned with OIG guidance and industry standards.
• Lead policy development, training, and guidance document lifecycle management.
• Manage HCP engagement program review for legitimate business need and FMV compliance.
• Design and administer a comprehensive compliance training program.
• Support risk-based monitoring and investigations as required.

Skills

Compliance operations

Regulatory knowledge

Cross-functional collaboration

Policy development

Investigations

Job description

Mineralys Therapeutics, Inc. is seeking a Director, Compliance to lead the company’s global compliance program. The role reports to the Vice President, Compliance and drives policy development, training, and monitoring across high‑risk activities.

The ideal candidate has extensive pharmaceutical compliance experience, including HCP engagement, FMV processes, and investigations, with a track record of timely program improvements and collaboration across functions.