Clinical Research Coordinator — Drive Trial Operations & Compliance

Advancedderm; South Carolina; Vor Ort; USD 42.000 - 66.000; Vollzeit

Benefits dieser Stelle

401K/PTO/Vacation/Benefit Packages

Zusammenfassung

Advancedderm is seeking a Clinical Research Coordinator (CRC) to support the Principal Investigator and the Director of Clinical Research in day-to-day trial activities, ensuring regulatory compliance and accurate study documentation. The CRC will help manage regulatory binders, source documents, and CRFs, while coordinating with sponsors, sites, and study personnel to maintain study timelines.

You will assist with feasibility, IRB submissions, participant recruitment, consent processes, data

Qualifikationen

• HIPAA compliance and privacy awareness
• Time management and prioritization
• Attention to detail and accuracy
• Professional ethics and discretion
• Strong communication skills

Aufgaben

• Coordinate with PI, department, and administration to ensure regulatory compliance and adherence to applicable regulations and policies
• Assist PI with study feasibility assessments and protocol reviews
• Prepare IRB submissions and other regulatory documents as required by the protocol
• Maintain regulatory binders and study files, source documents, and CRF completion
• Recruit, screen and consent study participants or volunteers; coordinate visits and assessments
• Collect data, perform assessments, and manage study timelines and enrollment logs

Jobbeschreibung

Advancedderm is seeking a Clinical Research Coordinator (CRC) to support the Principal Investigator and the Director of Clinical Research in day-to-day trial activities, ensuring regulatory compliance and accurate study documentation. The CRC will help manage regulatory binders, source documents, and CRFs, while coordinating with sponsors, sites, and study personnel to maintain study timelines.

You will assist with feasibility, IRB submissions, participant recruitment, consent processes, data