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(Admin) to support Regulatory Compliance Review (RCR) operations. This role ensures adherence to international guidelines by managing essential document processes and facilitating communication across project teams.
If you’re passionate about regulatory documentation and global compliance, this is your opportunity to grow in a world-class organization with remote flexibility.
📋 Key Responsibilities
- Perform global regulatory compliance reviews of essential documents for study-specific Essential Document Checklists (EDCs).
- Respond to queries from project teams on EDC requirements and regulatory standards.
- Facilitate discussions on deviations from RCR processes, ensuring compliance and transparency.
- Manage and coordinate the Essential Document Checklist Process efficiently.
- Maintain up-to-date knowledge of PPD SOPs, client directives, and global regulatory guidelines.
- Review, finalize, and post EDCs with accuracy and timeliness.
- Support documentation consistency, version control, and process adherence.
🎓 Qualifications and Experience
Education:
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- Bachelor’s degree in Science, Pharmacy, Life Sciences, or related discipline.
Experience:
- 1 to 3 years of relevant regulatory affairs or clinical documentation experience.
Key Skills:
- Excellent written and verbal English communication.
- Strong attention to detail, editorial accuracy, and organizational discipline.
- Proficient in Microsoft Word, Excel, PowerPoint, and adaptable to new digital tools.
- Working knowledge of global regulatory submission processes.
- Analytical and problem-solving mindset with collaborative team spirit.
💼 Benefits of Working with PPD
- 100% remote work flexibility with structured career growth.
- Exposure to global regulatory frameworks and clinical documentation systems.
- Work-life balance with standard weekday schedules.
- Access to continuous learning and upskilling programs.
- Inclusive and collaborative work environment.
🚀 How to Apply
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