Clinical Regulatory Associate – IRB Submissions & Compliance

Kids for the Future; Orlando (FL); On-site; USD 60,000 - 76,000; Full time

Job summary

Charter Research in Orlando, FL is seeking a Regulatory Associate to manage regulatory packets and IRB submissions for clinical trials. The role emphasizes maintaining audit-ready regulatory books and coordinating with sponsors and IRB across study activations.

Ideal candidates have 1 year of clinical research experience, strong organizational skills, and the ability to manage multiple tasks while ensuring regulatory compliance and data integrity.

Qualifications

• 1 year of clinical research experience preferred.
• Ability to manage multiple tasks and deadlines.
• Strong planning and organizational skills; attention to detail.

Responsibilities

• Prepare regulatory documents for IRB submissions and sponsor communications.
• Review informed consent form drafts and coordinate revisions with operations, IRB, and sponsor.
• Inform operations of IRB approvals, amendments, and required trainings; maintain audit-ready files.

Skills

Multitasking

Planning & organization

Verbal & written communication

Team collaboration

Integrity & confidentiality

Education

2 Year Degree

Job description

Charter Research in Orlando, FL is seeking a Regulatory Associate to manage regulatory packets and IRB submissions for clinical trials. The role emphasizes maintaining audit-ready regulatory books and coordinating with sponsors and IRB across study activations.

Ideal candidates have 1 year of clinical research experience, strong organizational skills, and the ability to manage multiple tasks while ensuring regulatory compliance and data integrity.