Clinical Research Data & Regulatory Specialist

Mary Bird Perkins Cancer Center; Baton Rouge (LA); On-site; USD 50,000 - 65,000; Full time

Job summary

Mary Bird Perkins Cancer Center seeks a Data and Regulatory Coordinator to support clinical trials through regulatory documentation, IRB submissions, and sponsor communications. The role collaborates with the Clinical Research team and Principal Investigator to ensure protocol compliance across sites.

The candidate will maintain protocol-specific information, assist with regulatory submissions, and manage trial documentation in line with applicable laws and center policies.

Qualifications

• Knowledge of clinical research regulations and trial conduct.
• Experience with regulatory submissions and IRB processes.
• Ability to maintain protocol and regulatory documentation.

Responsibilities

• Collaborate with Clinical Research team and PI to ensure protocol compliance.
• Maintain IRB documents, regulatory and protocol records for trials.
• Coordinate communication between Clinical Research and sponsors.

Skills

Regulatory knowledge

Clinical research

IRB procedures

Regulatory submissions

Communication

Education

Bachelor's degree or equivalent

Science health-care credential

Professional certifications preferred

Job description

Mary Bird Perkins Cancer Center seeks a Data and Regulatory Coordinator to support clinical trials through regulatory documentation, IRB submissions, and sponsor communications. The role collaborates with the Clinical Research team and Principal Investigator to ensure protocol compliance across sites.

The candidate will maintain protocol-specific information, assist with regulatory submissions, and manage trial documentation in line with applicable laws and center policies.