Senior Technology Auditor

The Senior Technology Quality Auditor will have the experience and knowledge to provide guidance and facilitate the effective preparation, management and follow up of internal and supplier technology audits. Will exhibit a high degree of flexibility and initiative, demonstrate the ability to follow up on multiple tasks and projects, and possess the ability to handle confidential information diplomatically.

​Skills:

• Excellent interpersonal, verbal and written communication skills
• Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
• Experience with Microsoft based applications and ability to learn internal and supplier computer systems
• Willingness to work effectively with multiple supervisors in a matrix environment and to value the importance of teamwork
• Ability to develop relationships with culturally diverse stakeholders, including Parexel team members and sponsor representatives
• Ability to work professionally with highly confidential information
• Flexibility and ability to adjust to changing priorities and unforeseen events
• Excellent time management skills and the ability to follow-up on multiple tasks and projects
• Ability to diplomatically address sensitive issues confidentially and professionally
• A team player with a positive attitude
• Ability to work consistently in a fast-paced environment

Knowledge and Experience:

• Strong knowledge of GxP, industry standards, applicable international technology compliance regulations

• Must be detail oriented and able to maintain a ‘big picture’ overview during a sponsor audit or inspection

• Ability to follow up on multiple tasks and projects, and to handle confidential information diplomatically

• Familiar in technology as it relates to clinical trial activities, including System Life Cycle process and applicable GCP regulations pertaining to Computer Systems

Education:

• Educated to degree level (technology, biological science, pharmacy or other health related discipline preferred) or equivalent qualification or clinical research experience

• a few years of experience in Quality Assurance, auditing, relevant Quality Management and clinical trial support