Clinical Research Coordinator: Impactful Trials & Care

ActivMed Practices & Research, LLC.; Decatur (GA); On-site; USD 52,000 - 68,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Short-term disability insurance

Long-term disability insurance

Health Savings Accounts

Supplemental insurances

401k plan with safe harbor match

Job summary

Alcanza Clinical Research seeks a Clinical Research Coordinator to ensure study execution in line with GCP, ICH, HIPAA, FDA regulations and SOPs. The CRC will work with site teams across multiple locations to screen, consent, and monitor study participants.

Responsibilities include data entry, vital signs, ECGs, and coordinating with sponsors and IRB. Prior experience and bilingual skills are valued. Equal opportunity employer.

Qualifications

• Medical Assistant diploma, LPN/LVN, EMT credential OR Associate’s degree is required.
• Minimum 1 year of clinical research or clinical experience preferred.
• Bi-lingual (English/Spanish) proficiency is a plus.

Responsibilities

• Screen patients for study enrollment.
• Obtain patient consents.
• Follow-up patient visits and chart documentation.
• Enter data in EDC and respond to queries.

Skills

MS Office proficiency

Electronic health records

Data entry accuracy

Strong communication

Organization & detail

Bilingual communication

Education

Associate’s degree

Medical Assistant diploma

LPN/LVN credential

EMT credential

Tools

Electronic Health Records (EHR)

EDC systems

MS Office

Job description

Alcanza Clinical Research seeks a Clinical Research Coordinator to ensure study execution in line with GCP, ICH, HIPAA, FDA regulations and SOPs. The CRC will work with site teams across multiple locations to screen, consent, and monitor study participants.

Responsibilities include data entry, vital signs, ECGs, and coordinating with sponsors and IRB. Prior experience and bilingual skills are valued. Equal opportunity employer.