Clinical Research Coordinator — Multisite Trials & Impact

Accel Research Sites; DeLand (FL); On-site; USD 42,000 - 56,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Short-term disability

Long-term disability

Health savings accounts

401k plan with safe harbor match

Job summary

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

Responsibilities include patient screening, obtaining consents, follow-up visits, data entry in EDC, vital signs and ECGs, and coordination with the site team. Prior clinical research or clinical experience is required, with a Medical Assistant diploma or equivalent credentials preferred.

Qualifications

• A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate’s degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and experience, is required.
• Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred.
• Bi-lingual (English / Spanish) proficiency is a plus.

Responsibilities

• Screening of patients for study enrollment.
• Patient consents and follow-up visits.
• Documenting in source clinic charts and entering data in EDC.
• Obtaining vital signs and ECGs; basic lab procedures per protocol.

Skills

Clinical research procedures

Basic clinical procedures

Bi-lingual English/Spanish

Organization & detail orientation

MS Office / EHR proficiency

Strong communication

Education

Associate’s degree

Medical Assistant diploma

LPN/LVN credential

EMT credential

Job description

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

Responsibilities include patient screening, obtaining consents, follow-up visits, data entry in EDC, vital signs and ECGs, and coordination with the site team. Prior clinical research or clinical experience is required, with a Medical Assistant diploma or equivalent credentials preferred.