Overview

Are you a seasoned drug safety professional ready to shape the future of technology? micro1 is looking for skilled Pharmacovigilance Experts to join us on a fully remote contractor basis from anywhere in the world. You do not need any prior background in artificial intelligence because your core domain knowledge is what truly drives this project. By sharing your expertise, you will help train next-generation AI systems to reason and perform with real world medical data. This unique freelance opportunity lets you combine your regulatory safety background with cutting edge innovation.

Key Responsibilities

Author and review evaluation tasks using DSURs, PSURs, PBRERs, safety data, and case level records.
Apply expert judgment to check the accuracy of interval safety findings, signal evaluations, and benefit risk conclusions.
Evaluate template and structural conformity against ICH E2F and ICH E2C guidelines.
Verify proper section content, presentation of cumulative versus interval data, and the completeness of all appendices.
Reconcile figures and case counts with meticulous attention to detail.

Requirements

Extensive professional background in pharmacovigilance and drug safety.
Demonstrated experience authoring and reviewing complex safety reports.
Deep familiarity with ICH E2F and ICH E2C regulatory standards.
Exceptional written and verbal communication skills in English.
A strong commitment to data quality and analytical precision.

What You'll Gain

The chance to influence how advanced AI models understand and process medical safety data.
Complete location independence with a 100% remote schedule.
Flexible contracting terms that fit around your professional lifestyle.
Collaboration with forward thinking innovators at the intersection of healthcare and technology.