This person will be responsible for attending meetings with customers to discuss, coordinate and report on the status of clinical trial studies.

Requires an individual with excellent time management, multitasking and customer facing skills.

Ideal candidate will have experience with quality in a CAPS or CLIA environment.

Client will consider candidates from pharmaceutical, medical, food or other industries that are heavily regulated.

Essential duties:

• Conduct work as identified on the audit activity list
• Contributes to global QA policies on interpretation/ application of regulations
• Provide support to projects Support team in CAPA plan creation
• Hosts external audits/inspections e.g. regulatory inspections, strategic clients. Assists with the facilitation of audit responses
• Supports the QA–to-QA relationship with key client(s)
• Supports the reporting of quality metrics and implementation of necessary corrective actions and/or process improvements via appropriate forum (e.g. Monthly Reports, Site Quality Review, Liaison meetings)
• Other duties as assigned by management.