Regulatory Coordinator (Remote) - Clinical Research Compliance

MaziCTools; United States; Remote; USD 48,000 - 55,000; Full time

Job summary

A & J Personnel is seeking a Regulatory Coordinator to manage IRB submissions and ensure regulatory compliance for human subjects research. You will interpret guidelines, coordinate with IRBs, and work with study teams and sponsors to ensure proper documentation and reporting.

The role is entry-level, designed for individuals interested in clinical research and regulatory affairs, with opportunities to grow within a university setting that supports oncology and clinical trials.

Qualifications

• Bachelor degree or equivalent and one year of relevant experience.
• Experience with IRB processes and human subject research.
• Ability to interpret regulations and guidelines.
• Knowledge of Good Clinical Practice.

Responsibilities

• Interpret Code of Federal Guidelines and IRB policies and other regulatory approaches for human subjects research.
• Prepare protocol submissions through IRBs and regulatory offices, gather documentation, and prepare submission packages.
• Review documents with teams for accuracy and adherence to the Clinical Trial Administration Framework.

Skills

Communication skills

Attention to detail

Microsoft Office

Education

Bachelor Degree

Tools

Database experience

Job description

A & J Personnel is seeking a Regulatory Coordinator to manage IRB submissions and ensure regulatory compliance for human subjects research. You will interpret guidelines, coordinate with IRBs, and work with study teams and sponsors to ensure proper documentation and reporting.

The role is entry-level, designed for individuals interested in clinical research and regulatory affairs, with opportunities to grow within a university setting that supports oncology and clinical trials.