Clinical Research Coordinator: Multi-Site Trials

Alcanza Clinical Research; Town of Florida (NY); On-site; USD 50,000 - 70,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

401k with safe harbor match

Job summary

Alcanza Clinical Research is hiring a Clinical Research Coordinator (CRC) to support multi-site Phase I–IV studies. You will ensure study execution in line with GCP, ICH, HIPAA, FDA regulations and SOPs.

Responsibilities include patient screening, consent, visits, data entry, vitals/ECGs, basic lab procedures, and study documentation. Collaboration with site team and sponsors is essential.

Qualifications

• Minimum: Medical Assistant diploma, LPN/LVN, EMT credential OR Associate’s degree, plus 1 year clinical research or clinical experience.
• Proficiency in basic clinical procedures (vital signs, EKGs, phlebotomy) is preferred.
• Bi-lingual English/Spanish is a plus.

Responsibilities

• Screen patients for study enrollment and obtain informed consent.
• Perform vital signs, EKGs and basic lab procedures per protocol.
• Document in source charts and enter data in EDC; respond to data queries.

Skills

Medical procedures

Bi-lingual

Organizational skills

Attention to detail

Communication skills

HIPAA knowledge

Education

Medical Assistant diploma/LPN/LVN/EMT credential or Associate’s degree

Tools

Microsoft Office

Electronic Health Records (EHR)

Job description

Alcanza Clinical Research is hiring a Clinical Research Coordinator (CRC) to support multi-site Phase I–IV studies. You will ensure study execution in line with GCP, ICH, HIPAA, FDA regulations and SOPs.

Responsibilities include patient screening, consent, visits, data entry, vitals/ECGs, basic lab procedures, and study documentation. Collaboration with site team and sponsors is essential.