Regulatory Specialist

Overview

Role involves coordinating regulatory activities for clinical trials and ensuring compliance.

Ideal candidate should have 2+ years of experience in clinical research regulatory affairs.

Locations

• United States

Requirements

• 2 years experience in regulatory affairs
• Bachelor's degree preferred
• Understanding of FDA regulations and GCP
• Strong organizational skills
• Excellent communication abilities
• Legal authorization to work in the US required

Responsibilities

• Manage regulatory documentation
• Ensure compliance with regulations
• Prepare and submit regulatory documentation
• Collaborate with research teams
• Participate in audits
• Deliver regulatory training

Benefits

• Competitive compensation
• 401(k) plan
• Health insurance
• Paid time off
• Adoption assistance
• Disability coverage