Senior Regulatory Specialist - Remote Clinical Trials

DM Clinical Research; Houston (TX); Remote; USD 70,000 - 90,000; Full time

Job summary

A clinical research organization is seeking a Senior Regulatory Specialist to provide regulatory oversight for clinical trials. This remote position involves preparing and coordinating IRB submissions, ensuring regulatory compliance, and facilitating training for staff. Ideal candidates will have at least 2 years of clinical research experience along with strong communication and project management skills. Applicants should be able to manage time-sensitive projects effectively while maintaining a high degree of professionalism in interactions.

Qualifications

• 2+ years of clinical research coordinator experience or 3+ years of clinical regulatory experience.

Responsibilities

• Prepare and coordinate IRB submissions for protocol revisions.
• Ensure compliance with IRB and regulatory requirements.
• Facilitate training and supervision of regulatory staff.

Skills

Strong written and oral communication skills

Proven leadership skills in project management

Strong computer skills, including Microsoft Office

Job description

A clinical research organization is seeking a Senior Regulatory Specialist to provide regulatory oversight for clinical trials. This remote position involves preparing and coordinating IRB submissions, ensuring regulatory compliance, and facilitating training for staff. Ideal candidates will have at least 2 years of clinical research experience along with strong communication and project management skills. Applicants should be able to manage time-sensitive projects effectively while maintaining a high degree of professionalism in interactions.