Eblex Group · 10 hours ago
Regulatory Affairs Consultant
United States
Contract
Remote
Senior Level
$80/hr - $110/hr
5+ years expEblex Group is looking for an experienced Clinical Regulatory Affairs Consultant to support U.S.-based biotech clinical programs on a contract basis. This role focuses on IND-related activities, protocol support, and study start-up regulatory documentation for early-stage sponsors.
Hiring Manager
Shaun B.
Responsibilities
IND submissions, amendments, and annual reports
Regulatory input during protocol development and study start-up
Collaboration with clinical, medical, and CMC teams
FDA, ICH, and GCP compliance
Qualification
Required
5+ years in U.S. Clinical Regulatory Affairs
Hands-on IND experience
Biotech, pharma, or CRO background
Preferred
Contract / consulting experience preferred
Company
Eblex Group
We specialise in bringing together two worlds; Life Sciences and Technology and connecting the talent that drives innovation across them creating a faster, smarter, and more valuable experience for both clients and candidates.
2-10 employees
Funding
Current Stage
Early StageCompany data provided by crunchbase