Job Description
We are seeking qualified professionals in Pharmaceutical Regulatory Affairs and Drug Regulatory Science to collaborate with us as independent subject-matter experts on a project basis.
Our organization works with immigration attorneys and professionals to prepare credential evaluations and expert opinion reports used in U.S. employment-based immigration cases .
This role involves professional document review and regulatory expertise validation, not clinical practice or direct regulatory submission work.
Responsibilities
Selected experts may be asked to:
Review academic degrees, training, and certifications in regulatory affairs or pharmaceutical sciences
Evaluate professional experience related to drug development, regulatory compliance, or approval pathways
Assess qualifications against U.S. standards in pharmaceutical regulatory practice
Review job descriptions and confirm alignment with regulatory science functions
Contribute to or review structured Expert Opinion Letters for formal documentation
All assignments are document-based, confidential, and fully remote.