Overview
Work directly with the Global Audit Coordination Senior Manager to monitor and manage the Quality & Compliance Audit Program, supporting Project Managers and Sponsors with documentation, tracking, reporting and administrative tasks.
What you'll do
- Take primary responsibility for Audit Coordination and related activities, supporting the Global Audit Coordination Senior Manager, Project Managers and Sponsors according to ProPharma best practices.
- Communicate proactively with Project Managers and Sponsors regarding contract documents, proposals, assignment letters, purchase orders, change orders and other contract modifications.
- Generate documents including contract documents (NDA/CDA), proposals, change orders, affiliate agreements and assignment letters.
- Handle audit setup in DOT and Workday, support, time and expense review and approval, and invoice review and approval.
- Be an active participant in the Project Management of large audit projects.
- Develop, generate and/or maintain audit/project reports including the audit tracking log, personnel plan and utilization reports.
- Ensure all correct documentation is in place before project commencement in accordance with SOPs and/or client training requirements.
- Assist with specific project reporting needs.
- Perform other duties as assigned.
What you'll need
- Associate degree or equivalent work experience.
- Experience in a work-related customer service function.
- Computer data entry experience.
- Excellent proficiency with Microsoft Office Suite (Access, Outlook, Word, Excel).
- Proficient computer knowledge and keyboarding skills, including intermediate proficiency in Microsoft Office Suite.
- Intermediate database skills to enter and retrieve information from multiple databases including ProPharma CRM and ProPharma Accounting/Project Management software.
- Flexibility and adaptability to meet changing needs of the group.
- Strong verbal, written and interpersonal communication skills.
- Strong organization and prioritization skills with strong attention to detail.
- Ability to work independently and within a team.
- Ability to project professionalism and maintain composure in difficult situations and under stress.
- Exceptional customer service skills.
Nice to have
- 2 years of experience in a related field of expertise or 2 years of administrative experience.
- Experience within the Pharmaceutical/Medical Device Industry.
Details
- Working hours: UK hours preferred, with some flexibility.
- Remote working is supported; new hires within a reasonable commute of an office are encouraged to work on a hybrid basis as agreed with their manager.
Read the full description and apply on the company’s own careers page.