Senior Regulatory Document Coordinator

Roles & Responsibilities
• Support preparation, formatting, compilation, and filing of regulatory documents and submissions
• Coordinate regulatory documentation activities under guidance of senior regulatory staff
• Ensure accuracy, completeness, and compliance with applicable regulatory requirements
• Maintain regulatory documentation as per SOPs and internal quality standards
• Provide administrative and documentation support to regulatory and clinical teams
• Handle multiple documentation tasks across projects with strong organizational skills
• Collaborate effectively with internal teams, managers, and external stakeholders

Qualifications
• Minimum High School Diploma or equivalent (mandatory)
• Bachelor’s degree preferred in Pharmacy, Biotechnology, Biology, Microbiology, or Life Sciences

Experience
• Experience in regulatory documentation, clinical research support, or pharmaceutical/CRO environment preferred
• Freshers with strong documentation skills and MS Office proficiency may also be considered

Skills
• Strong communication and organizational skills
• Proficiency in MS Word, Excel, PowerPoint, and MS Office tools
• High attention to detail and document accuracy
• Basic understanding of regulatory documentation and SOP-driven processes
• Ability to manage multiple tasks under supervision
• Strong teamwork and professional collaboration skills

About the Organization
IQVIA is a global leader in clinical research, healthcare analytics, and technology solutions. The company supports the development and commercialization of innovative healthcare products through data-driven insights and scientific expertise.