Clinical Research Assistant — Impactful, Multi-Site Trials

ActivMed Practices & Research, LLC.; Jacksonville (FL); On-site; USD 22,000 - 32,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Disability insurance

Health Savings Account

401(k) with safe harbor match

Equal Opportunity Employer

Job summary

Alcanza Clinical Research is seeking a Research Assistant to support clinical site staff in performance of study activities and data collection. Responsibilities include supervising basic screening, patient follow-up, data entry in EDC, vital signs, and potentially blood draws under protocol guidance.

Required: High School diploma and 1 year of admin/clinical experience; bilingual English/Spanish a plus. We offer a collaborative team environment across multiple sites and comprehensive benefits.

Qualifications

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

Responsibilities

• Assist CRCs and site staff in study execution per protocol.
• Screen patients for enrollment and schedule visits.
• Document in source charts and enter data in EDC; answer queries.
• Obtain vital signs and ECGs; may perform blood draws.
• Prepare and ship lab specimens; maintain logs and charts.
• Maintain confidentiality and HIPAA compliance.
• Support recruitment and patient enrollment as needed.

Skills

Computer skills

Data entry

Communication

Multitasking

HIPAA compliance

Education

High School diploma

Bilingual English/Spanish

Tools

Microsoft Office

Electronic Health Records

EDC systems

Web applications

Job description

Alcanza Clinical Research is seeking a Research Assistant to support clinical site staff in performance of study activities and data collection. Responsibilities include supervising basic screening, patient follow-up, data entry in EDC, vital signs, and potentially blood draws under protocol guidance.

Required: High School diploma and 1 year of admin/clinical experience; bilingual English/Spanish a plus. We offer a collaborative team environment across multiple sites and comprehensive benefits.