Clinical Trial Operations Specialist I

FTCRUDE Fortrea CRU Inc.; Daytona Beach (FL); On-site; USD 42,000 - 54,000; Full time

Benefits offered by this job

Medical

Dental

Vision

Life insurance

401(k)

PTO

Job summary

Fortrea CRU Inc. is seeking an Operations Coordinator I for our Daytona Beach, FL site. The role focuses on hands-on participation with healthy volunteers, learning protocols, and supporting a fast-paced, team-oriented environment.

You will assist senior team members, coordinate study logistics, and ensure smooth operations across multiple trial types while maintaining regulatory compliance and participant safety.

Qualifications

• University/college degree in life science, pharmacy or related field preferred.
• Certification in allied health profession may substitute for degree.
• 1-2 years of professional work experience in clinical research.
• Basic knowledge of computers and programs (Word, Excel).
• Knowledge of drug development process, ICH Guidelines and GCP.
• BLS or CPR/AED certified.

Responsibilities

• Support practical/administrative activities for a clinical research trial.
• Assist senior study team members such as the Clinical Research Coordinator and Project Manager.
• Set up study logistics to ensure good flow and adequate resources.
• Create source documents, labels, and study-specific instructions.
• Prepare study schedules and orders for supplies/equipment.
• Coordinate with contracted services (labs, ECG).
• Train staff on study procedures and maintain training records.
• Coordinate participant check-in/discharge and resolve issues.
• Maintain accurate records and ensure participant safety and confidentiality.
• Assist with data tables, CRF completion, and protocol deviations.

Skills

Knowledge of FDA/ICH/GC P processes

Computer skills (Word, Excel)

BLS/CPR Certification

Education

Life science degree

Allied health certification

Tools

Microsoft Word

Microsoft Excel

Job description

Fortrea CRU Inc. is seeking an Operations Coordinator I for our Daytona Beach, FL site. The role focuses on hands-on participation with healthy volunteers, learning protocols, and supporting a fast-paced, team-oriented environment.

You will assist senior team members, coordinate study logistics, and ensure smooth operations across multiple trial types while maintaining regulatory compliance and participant safety.