Multisite Clinical Research Coordinator — Drive Trials

ActivMed Practices & Research, LLC.; South Carolina; On-site; USD 42,000 - 64,000; 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)

401k plan with safe harbor match

Job summary

Alcanza Clinical Research seeks a Clinical Research Coordinator (CRC) to ensure execution of assigned studies in compliance with GCP, ICH, HIPAA, and FDA regulations. The CRC will collaborate with site teams to screen patients, obtain consent, schedule visits, and manage data and source documentation.

The role requires basic clinical procedures (BP, vitals, EKGs, phlebotomy) and data entry, with emphasis on timely adverse event reporting, confidentiality, and high quality study conduct.

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.
• Patient follow-up visits.
• Documenting in source clinic charts.
• Entering data in EDC and answers queries.
• Obtaining vital signs and ECGs.
• May perform basic lab procedures per protocol (blood collection, centrifuge, storage and shipping).
• Updating and maintaining logs and charts.
• Scheduling subjects for study visits and reminders.
• Monitoring visits and resolving issues in a timely manner.
• Filing SAE/Deviation reports and reporting adverse events.
• Maintaining confidentiality of patients and company information.

Education

Medical Assistant diploma

LPN/LVN

EMT credential

Associate’s degree

Job description

Alcanza Clinical Research seeks a Clinical Research Coordinator (CRC) to ensure execution of assigned studies in compliance with GCP, ICH, HIPAA, and FDA regulations. The CRC will collaborate with site teams to screen patients, obtain consent, schedule visits, and manage data and source documentation.

The role requires basic clinical procedures (BP, vitals, EKGs, phlebotomy) and data entry, with emphasis on timely adverse event reporting, confidentiality, and high quality study conduct.