Clinical Research Assistant: Start in Study Coordination

Accel Research Sites; DeLand (FL); On-site; USD 32,000 - 48,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

401k with safe harbor match

Job summary

Accel Research Sites in DeLand, FL is seeking a Clinical Research Assistant / Medical Assistant to support CRCs, site staff, and investigators in line with GCP, ICH, HIPAA and FDA SOPs. Duties include patient screening, data entry in EDC, vital signs, ECGs, and coordinating visits.

The RA role involves lab tasks, charting, and maintaining logs while ensuring confidentiality and regulatory compliance. Strong organizational and communication skills are essential for success in a busy research site.

Qualifications

• High School diploma required.
• 1 year of administrative/clinical experience required.
• 1+ year in clinical research or clinical experience preferred.
• Bi-lingual English/Spanish is a plus.

Responsibilities

• Assist CRCs and site staff with study execution per protocol.
• Document in source charts and enter data in EDC; respond to queries.
• Obtain vital signs and ECGs; may perform blood draws and basic lab procedures.
• Schedule visits, reminders, and reschedule as needed; maintain logs and charts.
• Maintain confidentiality in accordance with HIPAA guidelines.

Skills

MS Office

Email

EHR

Web applications

Typing 40 wpm

Organizational skills

Communication

Interpersonal skills

Multitasking

HIPAA/privacy

Education

High School diploma

Job description

Accel Research Sites in DeLand, FL is seeking a Clinical Research Assistant / Medical Assistant to support CRCs, site staff, and investigators in line with GCP, ICH, HIPAA and FDA SOPs. Duties include patient screening, data entry in EDC, vital signs, ECGs, and coordinating visits.

The RA role involves lab tasks, charting, and maintaining logs while ensuring confidentiality and regulatory compliance. Strong organizational and communication skills are essential for success in a busy research site.