Impactful Multisite Clinical Research Coordinator

ActivMed Practices & Research, LLC.; Tampa (FL); On-site; USD 42,000 - 66,000; 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 Account (HSA)

Supplemental insurances

401k with safe harbor match

Job summary

Alcanza Clinical Research is seeking a Clinical Research Coordinator to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA regulations and SOPs.

You will screen patients for enrollment, obtain informed consent, schedule visits, collect data, and assist with monitoring and start-up activities across multiple programs. Bi-lingual English/Spanish is a plus and strong organizational skills are essential.

Qualifications

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

Responsibilities

• Screen patients for study enrollment.
• Obtain patient consent.
• Conduct follow-up visits and document in source charts.
• Enter data in EDC and respond to queries.
• Obtain vitals and ECGs; collect blood samples if required.
• Schedule subjects for visits and provide appointment reminders.
• Maintain logs and study-related documentation.
• Support site initiation visits and investigator meetings.

Skills

Bilingual English/Spanish

Strong organizational skills

Excellent communication skills

Ability to work independently

Proficiency with Microsoft Office & E-

Education

Associate’s degree

Medical Assistant diploma / LPN/LVN / EMT credential

Tools

Electronic health records (EHR)

Job description

Alcanza Clinical Research is seeking a Clinical Research Coordinator to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA regulations and SOPs.

You will screen patients for enrollment, obtain informed consent, schedule visits, collect data, and assist with monitoring and start-up activities across multiple programs. Bi-lingual English/Spanish is a plus and strong organizational skills are essential.