Jobs at Parexel
Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Audit Coordinator
Job ID R0000031037 , IndiaKey Accountabilities:
General Administrative Duties
Organize meetings and business trips, write meeting minutes, submit travel expenses, as required
Download and distribute regular reports, listings etc. utilizing appropriate technologies and systems
Provide support in the generation and analysis of reports and questionnaires, as required
Drive compilation of data and requested information for Management’s business needs
Assist with client deliverables, e.g. audit reports, metrics
Prepare/update/distribute departmental organization charts
Oversee and maintain relevant departmental Sharepoint folders/SharePoint access, as required
Support stakeholder review assignments for SOP reviews
Extract awarded signed audits report monthly in Planisware
Assist in Sponsor Audit and Regulatory Inspection (SAI), as required (e.g. extranet access, PMEX set-up, etc.)
Assist GxP audits with sample selection, coordination and follow up activities, as needed
Gather necessary documents such as CVs, JDs, and training packages to support an SAI
Contribute to Lessons Learned to ensure continuous quality improvement
Schedule QA Global calls
Utilize AI to support admin and QA personnel, e.g. potential efficiencies with RFI/RFP, project selection
Maintain applicable admin related MI/GI linked with QA SOPs
Metrics and Trending Support
Collect, analyze and interpret data from various sources
Generate reports and visualizations to effectively communicate trends, patterns and key performance indicators to stakeholders
Identify trends in quality metrics to highlight potential areas for improvement
Additional Accountability
Maintain relevant knowledge of appropriate GxP requirements and developments as they impact Parexel’s international SOPs and compliance with GxP.
Promote compliance within the company and represent QA
Develop and maintain network contacts with other Quality Assurance professionals
Work to support department efficiency through sharing knowledge/tasks
Support Activities for QA team and manage special projects as assigned (e.g. billable deliverable activities)
Develop guidance documentation, processes, and tools for administrative tasks, as assigned
Assist with QA data entries, as required
Build, develop, and maintain good working relationships with internal and external customer groups.
Work well in team environment.
Perform other quality related tasks or duties as assigned
Travel on assignments as required. Travel time could be up to 10%
Skills:
Sound organizational skills, ability to prioritize workload and manage multiple, potentially conflicting deadlines with attention to detail and within agreed timelines
Comprehensive knowledge of relevant Microsoft office software: Windows, Word, Excel, PowerPoint, Outlook
Excellent interpersonal, verbal and written communication skills
Ability to take initiative
Shows commitment to high quality work
Self-motivated with willingness to accept responsibilities and challenges
Flexible ‘can do’ attitude to problem solving and with respect to work assignments and new learnings
Experience with and ability to adhere to strict confidentiality requirements
Ability to remain calm under pressure
Willingness to work in a matrix environment and values the importance of teamwork
Global mindset; ability to work in a decentralized/remote team environment
Additional Skills:
Excellent Microsoft office skills
Excellent Microsoft Excel skills, including knowledge of formulas, pivots, look up tables and chart generation preferred.
Knowledge and Experience:
Preferred 1- 2 years of experience in Quality Assurance, relevant Quality Management and/or clinical trial support or administrative work
Knowledge of GxP, industry standards, applicable regional regulations
A team player with a positive attitude and detail oriented
Education:
Educated to degree level (technology, biological science, pharmacy or other health related discipline preferred) or equivalent qualification or clinical research experience
Strong command of written and spoken English language, local language proficiency as required.
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