Remote MRI Clinical Trials Regulatory Specialist

Stanford Reglab; United States; Remote; USD 90,000 - 130,000; Full time

Job summary

Stanford University’s Division of Body MR in Radiology seeks a Clinical Trials Regulator Specialist to coordinate regulatory planning and commercialization of ARPA-H LIGHT MRI lymphatic imaging technologies. Remote work is available.

The role emphasizes organizing IRB protocols, ARPA-H interactions, and drafting submissions for translational studies toward FDA approval, with a Bachelor’s degree and 3+ years in regulatory affairs or clinical trials expected.

Qualifications

• Bachelor’s degree and three years of related experience required.
• Experience with clinical trials operations or regulatory affairs preferred.
• Knowledge of FDA regulatory requirements and IRB processes.

Responsibilities

• Independently develop, draft and compile regulatory submissions for clinical trials.
• Coordinate study initiation and educate staff and sponsors on regulatory requirements.
• Manage meetings and ensure proper documentation and dissemination of results.

Skills

Excellent communication skills

Inter-personal skills

Customer service focus

Education

Bachelor’s degree

Tools

MS Office

Database applications

Job description

Stanford University’s Division of Body MR in Radiology seeks a Clinical Trials Regulator Specialist to coordinate regulatory planning and commercialization of ARPA-H LIGHT MRI lymphatic imaging technologies. Remote work is available.

The role emphasizes organizing IRB protocols, ARPA-H interactions, and drafting submissions for translational studies toward FDA approval, with a Bachelor’s degree and 3+ years in regulatory affairs or clinical trials expected.