Chief Clinical Compliance & Quality Lead

Charter Research; Orlando (FL); On-site; USD 130,000 - 190,000; Full time

Job summary

Charter Research, a Florida-based clinical research company, seeks a Compliance Director to lead the Compliance Team and oversee regulatory affairs, QA, and data integrity in accordance with ICH GCP, FDA guidelines, and Charter SOPs.

The role requires extensive clinical trials compliance experience, strong leadership, and the ability to drive company‑wide compliance initiatives. Orlando-based, on-site position with a focus on inspection readiness and regulatory excellence.

Qualifications

• Bachelor’s degree in health administration, regulatory studies, or related field.
• Master’s degree preferred in health admin, regulatory, or science.
• ACRP/ SOCRA/ CCRP-type certifications strongly preferred.

Responsibilities

• Lead the Compliance Team and oversee regulatory affairs, data management, QA, and compliance.
• Design and implement compliance plans, risk analyses, and CAPA tracking.
• Ensure inspection readiness across all sites with internal and sponsor audits, FDA inspections.

Skills

Audit leadership

Regulatory knowledge

Data integrity

Quality Assurance

GCP compliance

FDA inspections

Team leadership

Education

Bachelor’s degree in health administration or related field

Master’s degree in related field

ACRP/SOCR ACRP-CP/CCRC certification

Tools

SOP management tools

Job description

Charter Research, a Florida-based clinical research company, seeks a Compliance Director to lead the Compliance Team and oversee regulatory affairs, QA, and data integrity in accordance with ICH GCP, FDA guidelines, and Charter SOPs.

The role requires extensive clinical trials compliance experience, strong leadership, and the ability to drive company‑wide compliance initiatives. Orlando-based, on-site position with a focus on inspection readiness and regulatory excellence.