Clinical Research Regulatory Compliance Lead

Qualifications

• Bachelor's degree in Life Sciences or related field
• 5+ years of experience in clinical research
• Strong knowledge of regulatory requirements and compliance
• Experience with FDA and IRB submissions
• Excellent communication and leadership skills

Responsibilities

• Lead regulatory compliance initiatives for clinical trials
• Develop and implement compliance strategies
• Ensure adherence to FDA and IRB regulations
• Conduct training sessions for research staff
• Review and approve regulatory documents

Benefits

• Flexible work hours
• Opportunities for professional development
• Health and wellness programs
• Collaborative work environment
• Remote work options available