Clinical Research Assistant: Hands-On Trial Support & Impact

ActivMed Practices & Research, LLC.; Gilbert (AZ); On-site; USD 38,000 - 52,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

Life Insurance

Disability Insurance

Health Savings Account (HSA)

401(k) with match

Job summary

Alcanza Clinical Research is seeking a Research Assistant to support Clinical Research Coordinators and site staff in regulatory compliance and daily study activities. The role includes clinical tasks such as vital signs, ECGs, blood draws, data entry, and source document management.

The RA works under the Site Manager and investigators to ensure accurate enrollment, scheduling, and timely data queries, contributing to high-quality trial conduct across multiple sites.

Qualifications

• Requires a High School diploma and 1 year of admin/clinical experience.
• Phlebotomy experience is required.
• Bi-lingual English/Spanish is a plus.
• Familiarity with HIPAA and regulatory requirements is essential.

Responsibilities

• Assist with screening patients for study enrollment and follow-up visits.
• Document in source charts and enter data in EDC.
• Obtain vital signs, ECGs, and possibly perform blood draws.
• Maintain logs, schedules, and ensure timely study-related reporting.

Skills

Administrative skills

Clinical research basics

HIPAA compliance

Bi-lingual English/Spanish

Data entry / EDC

Strong communication

Attention to detail

Education

High School diploma

Tools

Microsoft Office

Electronic Health Records (EHR)

Data entry software

Job description

Alcanza Clinical Research is seeking a Research Assistant to support Clinical Research Coordinators and site staff in regulatory compliance and daily study activities. The role includes clinical tasks such as vital signs, ECGs, blood draws, data entry, and source document management.

The RA works under the Site Manager and investigators to ensure accurate enrollment, scheduling, and timely data queries, contributing to high-quality trial conduct across multiple sites.