Clinical Research Assistant: Grow with a Multi‑Site Trials Team

Accel Research Sites; Jacksonville (FL); On-site; USD 42,000 - 54,000; Full time

Benefits offered by this job

Medical insurance

401k plan with match

Job summary

Alcanza is a growing multi-site clinical research company providing support to CRCs, site managers and investigators across Phase I-IV studies. The Research Assistant performs clinical, lab, and administrative tasks to support site operations in compliance with GCP, ICH, HIPAA, and FDA regulations.

The RA assists with screening, visits, data entry in EDC, vital signs, specimen handling, and coordinating study activities while maintaining confidentiality and adhering to SOPs.

Qualifications

• A 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 by conducting study-related activities per protocol.
• Screen patients for study enrollment and coordinate follow-up visits.
• Document in source charts and enter data in EDC; respond to queries.
• Obtain vital signs and ECGs; may perform blood draws.
• Maintain logs, filing, and scheduling for study visits.

Skills

Administrative tasks

Data entry

Organization

Communication

Education

High School diploma

Tools

Microsoft Office

Electronic Health Records

EDC / data capture

Job description

Alcanza is a growing multi-site clinical research company providing support to CRCs, site managers and investigators across Phase I-IV studies. The Research Assistant performs clinical, lab, and administrative tasks to support site operations in compliance with GCP, ICH, HIPAA, and FDA regulations.

The RA assists with screening, visits, data entry in EDC, vital signs, specimen handling, and coordinating study activities while maintaining confidentiality and adhering to SOPs.