Job Summary

• The role involves coordinating serious and non-serious adverse events, protocol inquiries, and Data Safety Monitoring Board data for global pharmaceutical programs.
• Candidates will represent the organization at committee meetings, manage contractual documents like Confidentiality Disclosure Agreements, and ensure audit readiness for PV activities.
• This position requires maintaining strict accuracy in data entry, managing project budgets, and providing training to junior staff while adhering to FDA and ICH regulations.

Matching Summary

Skills & Requirements

Key Requirements

• High school diploma or equivalent
• At least 2 years of relevant experience
• Knowledge of FDA Regulations and ICH GCP

Work Rights