Clinical Research Assistant — Drive Multisite Trials

ActivMed Practices & Research, LLC.; Charleston (SC); On-site; USD 36,000 - 52,000; Full time

Benefits offered by this job

Medical, dental, vision

Life insurance

Short and long-term disability

401k with safe harbor match

Health savings accounts

Job summary

Alcanza Clinical Research is seeking a Research Assistant to support Clinical Research Coordinators, Site Manager, Principal Investigators, and other site staff in compliance with GCP, ICH, HIPAA, FDA regulations and SOPs at a multi-site clinical research network.

You will perform clinical, lab, and administrative tasks, assist with screening, follow-up visits, data entry in EDC, chart documentation, vital signs and potential blood draws, while maintaining patient confidentiality.

Qualifications

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

Responsibilities

• Assist CRCs and site staff with screenings and follow-up visits.
• Enter data in EDC and respond to queries.
• Obtain vital signs and ECGs; may perform blood draws.
• Maintain logs and filing; schedule visits and reminders.
• Ensure confidentiality and HIPAA compliance.

Skills

MS Office

Electronic Health Records

Data entry

Organization

Communication

Multitasking

HIPAA compliance

Bilingual English/Spanish

Education

High School Diploma

Tools

EDC systems

Job description

Alcanza Clinical Research is seeking a Research Assistant to support Clinical Research Coordinators, Site Manager, Principal Investigators, and other site staff in compliance with GCP, ICH, HIPAA, FDA regulations and SOPs at a multi-site clinical research network.

You will perform clinical, lab, and administrative tasks, assist with screening, follow-up visits, data entry in EDC, chart documentation, vital signs and potential blood draws, while maintaining patient confidentiality.