Clinical Research Coordinator - Multi-Site Trials

Accel Research Sites; Decatur (GA); On-site; USD 52,000 - 73,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Short/Long-term disability insurance

Health Savings Account

401k with safe harbor match

Job summary

Accel Research Sites in Decatur, GA is seeking a Clinical Research Coordinator to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.

In collaboration with other site team members, you will screen patients for enrollment, obtain consents, conduct follow-up visits, document in source charts, and enter data in EDC while maintaining study documentation and confidentiality.

Qualifications

• Minimum qualifications include a Medical Assistant diploma, LPN/LVN, EMT credential or an Associate’s degree with 1 year of clinical experience.
• Ability to perform basic clinical procedures (blood pressure, vitals, EKGs, phlebotomy) is highly preferred.
• Bi-lingual English/Spanish proficiency is a plus.

Responsibilities

• Screen patients for study enrollment and obtain informed consent.
• Conduct patient follow-up visits and schedule visits.
• Document in source charts and enter data in EDC.
• Obtain vital signs, ECGs, and basic lab procedures as per protocol.
• Maintain logs, manage study supplies and recruit patients as needed.
• Ensure compliance with GCP, ICH, HIPAA, and FDA SOPs.

Skills

Medical procedures

Typing 40+ wpm

Bilingual English/Spanish

Organizational skills

Written & verbal communication

HIPAA/GCP compliance

Education

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

Tools

Electronic health records (EHR)

MS Office / Web applications

Job description

Accel Research Sites in Decatur, GA is seeking a Clinical Research Coordinator to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.

In collaboration with other site team members, you will screen patients for enrollment, obtain consents, conduct follow-up visits, document in source charts, and enter data in EDC while maintaining study documentation and confidentiality.