Entry-Level Clinical Trials Operations Coordinator

Fortrea; Daytona Beach (FL); On-site; USD 42,000 - 64,000; Full time

Benefits offered by this job

Medical, Dental, Vision

401(K)

Paid time off

Employee recognition awards

Job summary

Fortrea, a leading Clinical Research Organization, seeks an Operations Coordinator I to support healthy volunteers through study setup, documentation, and coordination in a fast-paced team. Based in Daytona Beach, FL, this office/clinic role requires collaboration with CRU teams and adherence to GCP/ICH guidelines.

You will assist senior staff, manage study logistics, prepare source documents, and help ensure timely data capture and participant safety in a diverse range of trials.

Qualifications

• Bachelor’s degree or equivalent in Life Science, Pharmacy or related field.
• Experience in clinical research or pharmaceutical settings preferred.
• Familiarity with FDA, ICH and GCP guidelines.
• BLS/CPR certification or equivalent is preferred.
• Strong computer skills including Word and Excel.

Responsibilities

• Provide practical/administrative support for a clinical trial.
• Assist senior study team members and act as back-up to the CR Coordinator.
• Set up study logistics and ensure adequate resources.
• Create source documents, labels, and study instructions.
• Coordinate participant check-in/discharge and assist with issues.

Education

University/college degree in life science, pharmacy or related field

Certification in a related allied health profession

2 years' experience in related fields (pharma, lab, data analysis) in lieu of degree

Basic knowledge of computers (Word, Excel)

Knowledge of drug development process, ICH and GCP

Basic Life Support Skills (BLS) or CPR/AED certified

Tools

Microsoft Word

Microsoft Excel

Job description

Fortrea, a leading Clinical Research Organization, seeks an Operations Coordinator I to support healthy volunteers through study setup, documentation, and coordination in a fast-paced team. Based in Daytona Beach, FL, this office/clinic role requires collaboration with CRU teams and adherence to GCP/ICH guidelines.

You will assist senior staff, manage study logistics, prepare source documents, and help ensure timely data capture and participant safety in a diverse range of trials.