Clinical Research Coordinator | 4-Day Week & Benefits

Articularis Healthcare Group Inc; Summerville (SC); On-site; USD 42,000 - 64,000; Full time

Benefits offered by this job

4-day work week

Benefits package including medical,3—d

Job summary

Articularis Healthcare Group in Summerville, SC is seeking a full-time Clinical Research Coordinator to support regulatory filings, trial start-up, and ongoing study data management.

You will prepare FDA 1572 forms, assist with IND submissions, coordinate IRB activities, monitor safety data, ensure HIPAA compliance, and maintain Investigator Site Files while supporting patient recruitment and site operations.

Qualifications

• Associates degree with 2 years' experience in a medical/clinical setting.
• Experience with regulatory documentation and FDA processes.
• Strong verbal and written communication.

Responsibilities

• Prepare regulatory documentation for study start-up (FDA 1572, IND, IRB).
• Coordinate regulatory activities and day-to-day site operations.
• Track licenses, CVs, and staff documentation.
• Maintain safety reports and data queries.
• Ensure HIPAA compliance and patient confidentiality.
• Support monitor visits and audits.
• Assist with patient recruitment strategies.

Skills

Regulatory docs

HIPAA compliance

Communication skills

Education

Associates degree

Tools

Microsoft Office

Job description

Articularis Healthcare Group in Summerville, SC is seeking a full-time Clinical Research Coordinator to support regulatory filings, trial start-up, and ongoing study data management.

You will prepare FDA 1572 forms, assist with IND submissions, coordinate IRB activities, monitor safety data, ensure HIPAA compliance, and maintain Investigator Site Files while supporting patient recruitment and site operations.