Pharmacovigilance Regulatory Intelligence

About the work from home job/internship

Selected intern's day-to-day responsibilities include

1. Monitor official pharmacovigilance, regulatory, health authority, and medical device safety update sources such as FDA, EMA, MHRA, Health Canada, TGA, HSA, Swissmedic, SFDA, and other relevant global regulators.

1. Validate whether the platform is correctly capturing new updates from these sources, including title, source, country/region, date, update type, urgency, affected PV roles, workflow relevance, and required action.

1. Review AI-generated or system-generated summaries and check that they are factually aligned with the original regulatory source before publication or escalation.

1. Classify updates by pharmacovigilance relevance, such as ICSR reporting, signal detection, risk management, labeling, local affiliate compliance, device vigilance, inspection readiness, AI/GxP governance, and regulatory intelligence monitoring.

Prepare concise impact notes explaining why an update matters, who it impacts, and what action a PV, regulatory, or compliance team may need to take.

1. Maintain a daily tracker of sources checked, updates found, updates captured by the system, missing updates, incorrect classifications, duplicates, and items requiring review.

1. Support weekly digest preparation by identifying high-priority updates for different user groups such as QPPV, Regulatory Intelligence Lead, Signal Management Lead, PV Quality Lead, and Device Vigilance Lead.

1. Help improve content quality, tagging accuracy, website freshness, and user relevance by providing structured feedback on gaps, outdated entries, unclear summaries, or missed regulatory updates.

Skill(s) required

Market research Medical Writing Pharmacovigilance Regulatory Affairs

Who can apply

Only those candidates can apply who