Clinical Research Coordinator — Multisite Trials Compliance

Accel Research Sites; Lakeland (FL); On-site; USD 45,000 - 60,000; Full time

Benefits offered by this job

Health insurance

Dental coverage

Vision coverage

Life insurance

Disability insurance

401k plan

HSA

Job summary

Accel Research Sites is seeking a Clinical Research Coordinator in Lakeland, FL to support multiple Phase I-IV studies. The CRC will ensure study execution in line with GCP, ICH, HIPAA, FDA regulations and SOPs, working with the operations team.

Responsibilities include patient screening and consent, follow-up visits, data entry in EDC, vital signs/ECGs, and maintaining study logs and supplies while communicating with sponsors and investigators.

Qualifications

• Medical Assistant diploma or higher with clinical background.
• At least 1 year of clinical research or clinical experience.
• Bi-lingual English/Spanish is a plus.

Responsibilities

• Screen patients for study enrollment.
• Obtain patient consents and follow-up visits.
• Document data in source charts and EDC systems.
• Record vital signs and ECGs; perform basic lab procedures.
• Maintain logs, study supplies, and adverse event reporting.

Education

Medical Assistant diploma

LPN/LVN credential

EMT credential

Associate0s degree

Tools

EDC systems

Microsoft Office

EHR

Job description

Accel Research Sites is seeking a Clinical Research Coordinator in Lakeland, FL to support multiple Phase I-IV studies. The CRC will ensure study execution in line with GCP, ICH, HIPAA, FDA regulations and SOPs, working with the operations team.

Responsibilities include patient screening and consent, follow-up visits, data entry in EDC, vital signs/ECGs, and maintaining study logs and supplies while communicating with sponsors and investigators.