Director, Quality Management.

Facilitation of professional development and career advancement of Quality Management staff Administrative supervision of Quality Management staff, jointly with Senior Director Quality Management Participation in recruitment of Quality Management (QM) staff Facilitation of initial and ongoing training of Quality Management staff Oversight of initial and ongoing training of PSI Operations employees in quality management topics Quality Management: Facilitation of regulatory agency inspections of PSI Facilitation of regulatory agency inspections of PSI-managed trial sites, including follow-up Participation in hosting client/third party audits of PSI, including follow-up Oversight of CAPA investigations management Management of investigations of suspected research misconduct, jointly with Senior Director Quality Management Backup responsibility for review of draft Quality Systems Documents (QSDs), including newly developed and revised QSDs Backup responsibility for approval of Quality Systems Documents Oversight of vendor qualification Oversight of computer systems validation documentation review Oversight of the process of providing assistance and feedback to all Company staff with regards to various GXP, regulatory compliance, and other QM matters May act as the primary QM contact for PSI Operations divisions and working groups/task forces with regard to various Corporate projects requiring QM Quality Assurance Auditing: Development and implementation of the annual audit plan Management of QA audits contracted to PSI Oversight of the preparation and maintenance of internal and contracted quality assurance audits documentation Business Development: May be recruited by Business Development for client meetings and vendor shows Qualifications: College or university degree MD, PharmD or degree in life sciences is a plus Minimum 7 years of experience in Clinical Research Minimum 5 years industry experience in the capacity of a QA auditor or equivalent Must have experience in planning, conducting and reporting all types of quality assurance audits Auditing experience in USA Excellent knowledge of ICH GCP guidelines, FDA/ EMA regulations, and applicable local regulations Team oriented with superior communication and interpersonal skills Strong time management, organizational, planning and presentation skills Demonstrated ability to meet tight deadlines, multi-task/be flexible and thrive in a fast-paced work environment Intermediate proficiency in MS Office (Word, Excel Power Point, Outlook) Must be a reasonably effective public speaker #J-18808-Ljbffr