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ProPharma Group

Regulatory sciences consultant for life sciences

Global Administrative Coordinator - Audit

Administrative SupportConfirmed live in the last 24 hours
Full-timeIndiaNo salary listed

About the Job

Requirements

  • Associate degree or equivalent work experience.
  • Experience in a work-related customer service function.
  • Computer data entry experience.
  • Excellent proficiency with Microsoft Office Suite, including Microsoft Access, Outlook, Word, and Excel.
  • Proficiency with computer keyboarding and intermediate proficiency in Microsoft Office Suite to create client documents and reports.
  • Intermediate database skills to enter and retrieve information from multiple databases, including ProPharma CRM and ProPharma Accounting/Project Management software.
  • Ability to work independently and within a team.
  • Ability to adapt to changing group needs.
  • Strong verbal, written, and interpersonal communication skills.
  • Strong organization, prioritization, and attention to detail.
  • Ability to create documents and reports with attention to detail.
  • Ability to maintain professionalism and composure in difficult or stressful situations.
  • Customer service skills.

Responsibilities

  • Take primary responsibility for audit coordination and related activities, supporting the Global Audit Coordination Senior Manager, Project Managers, and Sponsors according to current company best practices.
  • Communicate with Project Managers and Sponsors about contract documents, proposals, assignment letters, purchase orders, change orders, and other contract modifications.
  • Generate contract documents, including nondisclosure/confidentiality agreements, proposals, change orders, affiliate agreements, and assignment letters.
  • Set up audits in DOT and Workday; support time and expense review and approval, and invoice review and approval.
  • Participate in project management for large audit projects.
  • Develop, generate, and maintain audit and project reports, including the audit tracking log, personnel plan, and utilization reports.
  • Ensure required documentation is in place before project commencement in accordance with standard operating procedures and client training requirements.
  • Assist the Global Audit Coordination Senior Manager, Project Managers, and Sponsors with project reporting needs.
  • Perform other duties as assigned.

Desired Qualifications

  • Two years of experience in a related field of expertise or two years of administrative experience.
  • Experience in the pharmaceutical or medical device industry.

About the Company

ProPharma Group

Regulatory sciences consultant for life sciences

ProPharma Group provides regulatory sciences consulting and related services for drugs, biologics, medical devices, and diagnostics on a global scale. Its offerings cover the full lifecycle, from early development and clinical trials to regulatory approval and post-market activities. The company’s services include regulatory sciences, clinical research, quality and compliance, pharmacovigilance, medical information, and R&D technology, delivered by a team of over 2,500 professionals with more than 20 years of operation. ProPharma Group differentiates itself by providing expert, end-to-end regulatory and life sciences solutions across multiple product types and stages, helping pharmaceutical, biotechnology, and medical device companies navigate complex regulatory and compliance challenges. The goal is to help clients bring safe and compliant products to market efficiently while maintaining ongoing lifecycle support.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Raleigh, NC
Founded
2001

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