Clinical Research Coordinator — Multisite Trials

Accel Research Sites; Clearwater (FL); On-site; USD 52,000 - 65,000; Full time

Benefits offered by this job

Medical, dental, vision

401k plan with safe harbor match

Short and long-term disability

Job summary

Accel Research Sites in Clearwater is seeking a Clinical Research Coordinator to support multiple Phase I-IV studies under GCP/ICH/FDA. You will screen patients, obtain consent, collect data, and ensure protocol adherence at the Tampa Bay Medical Research site.

The role requires at least 1 year in clinical research or clinical experience, with medical assistant or nursing credentials preferred. On-site position with a comprehensive benefits package.

Qualifications

• Minimum qualifications include a Medical Assistant diploma, LPN/LVN, EMT credential or an Associate’s degree with 1 year of clinical experience.
• Proficiency with basic clinical procedures (blood pressure, vitals, EKGs, phlebotomy).
• Bi-lingual English/Spanish is a plus and HIPAA compliant practice required.

Responsibilities

• Screen patients for study enrollment and obtain consent.
• Schedule visits, conduct follow-ups, and reminders for subjects.
• Enter data in EDC and respond to queries.
• Obtain vital signs, EKGs, and basic lab procedures per protocol.
• Maintain logs, source documents and study-specific supplies.
• Ensure ALCOAC documentation and maintain confidentiality.
• Coordinate with investigators, staff, and sponsors; attend training and site visits.

Skills

Clinical research experience

Bilingual English/Spanish

HIPAA compliance

Data entry (EDC)

Microsoft Office

Communication

Organizational skills

Education

Medical Assistant diploma/LPN/LVn/EMT credential or Associate’s degree

Tools

Electronic Health Records

Microsoft Office

Source documentation

Job description

Accel Research Sites in Clearwater is seeking a Clinical Research Coordinator to support multiple Phase I-IV studies under GCP/ICH/FDA. You will screen patients, obtain consent, collect data, and ensure protocol adherence at the Tampa Bay Medical Research site.

The role requires at least 1 year in clinical research or clinical experience, with medical assistant or nursing credentials preferred. On-site position with a comprehensive benefits package.