Clinical Research Coordinator - Multisite Trials & Compliance

Alcanza Clinical Research, LLC; Lakeland (FL); On-site; USD 48,000 - 64,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Disability insurance

401k with match

Job summary

Alcanza Clinical Research, LLC is seeking a Clinical Research Coordinator to ensure proper execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA regulations and SOPs. The role supports patient screening, consent, visits and data entry at Accel Research Sites in Lakeland, FL.

The position requires a Medical Assistant diploma or equivalent with at least 1 year of clinical research or clinical experience, and proficiency in basic procedures. Bilingual English/Spanish is a plus.

Qualifications

• Minimum 1 year of clinical research or clinical experience required.
• Proficiency with basic clinical procedures (blood pressure, vitals, EKGs, phlebotomy) preferred.
• Bi-lingual English/Spanish a plus.

Responsibilities

• Screen patients for study enrollment and obtain consent.
• Conduct patient visits and follow-up.
• Document in source charts and enter data in EDC.
• Obtain vital signs and ECGs; collect blood specimens when needed.
• Maintain logs, study supplies, and complete start-up activities as required.
• Monitor for adverse events and report deviations to sponsor/IRB as needed.

Skills

Microsoft Office

EHR systems

Documentation

Communication

HIPAA compliance

Multitasking

Team collaboration

Problem solving

Education

Medical Assistant diploma / LPN/LVN / EMT credential / Associate's degree

Tools

Electronic health records (EHR)

Job description

Alcanza Clinical Research, LLC is seeking a Clinical Research Coordinator to ensure proper execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA regulations and SOPs. The role supports patient screening, consent, visits and data entry at Accel Research Sites in Lakeland, FL.

The position requires a Medical Assistant diploma or equivalent with at least 1 year of clinical research or clinical experience, and proficiency in basic procedures. Bilingual English/Spanish is a plus.