Senior Manager Quality Compliance (Rare Disease)

This senior quality compliance role focuses on supporting clinical trial work in rare disease by giving independent quality guidance and overseeing programs across the clinical development lifecycle. Day to day, it includes planning, carrying out, and reporting on risk-based GCP audits for sites, affiliates, service providers, and studies, as well as helping with outsourced audits. The position also involves supporting regulatory inspections and reviewing responses to health authorities, including work on root cause analysis and corrective and preventive actions. The advert names GCP knowledge and experience with audits, inspection support, and quality oversight as key parts of the work. It does not state a specific degree, certification, years of experience, or language requirement. The role is remote, and the contract is full-time. Although the job is based in Washington, D.C., the listing says the work location type is remote. It appears suited to someone with strong quality compliance experience who can advise independently and work across clinical development programs.