Multisite Clinical Research Coordinator

ActivMed Practices & Research, LLC.; Charleston (SC); On-site; USD 42,000 - 65,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Disability insurance

401k plan with safe harbor match

Job summary

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

The role involves screening patients, obtaining consents, data entry, vital signs/ECGs, and coordinating visits, logs, and investigations with ALCOAC principles. A Medical Assistant diploma or equivalent plus 1 year of clinical experience is required.

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.
• 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, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up.
• Requesting and tracking medical record requests.
• Updating and maintaining logs, chart filings.
• Maintaining & ordering study specific supplies.
• Scheduling subjects for study visits and conducts appointment reminders.
• Building/updating source as needed.
• Conducting monitoring visits and resolves issues as needed in a timely manner.
• Ensuring study related reports and patient results are reviewed by investigator in a timely manner.
• Filing SAE/Deviation reports to Sponsor and IRB as needed.
• Documenting and reporting adverse events.
• Reporting non-compliance to appropriate staff in timely manner
• Maintaining positive and effective communication with clients and team members.

Skills

Computer proficiency

Typing 40+ wpm

EHR systems

Education

Medical Assistant diploma

LPN/LVN credential

EMT credential

Associate’s degree

Tools

Microsoft Office

Electronic Health Records

Job description

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

The role involves screening patients, obtaining consents, data entry, vital signs/ECGs, and coordinating visits, logs, and investigations with ALCOAC principles. A Medical Assistant diploma or equivalent plus 1 year of clinical experience is required.