Clinical Research Associate — On-Site Monitor (Orlando)

ICON plc; Orlando (FL); Presencial; USD 70.000 - 95.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health insurance

Retirement planning

Employee Assistance Programme

Life insurance

Flexible benefits

Descripción de la vacante

ICON Strategic Solutions in Orlando, FL is seeking a Clinical Research Associate to support site monitoring across multiple therapeutic areas. You will ensure regulatory compliance, maintain CTMS/eTMF documentation and drive safe, timely data entry while coordinating with sponsor teams.

The ideal candidate has 2+ years of on-site monitoring experience, a Life Sciences degree or RN, and is willing to travel up to 75% across the southeast region. Visa sponsorship is not provided.

Formación

• Bachelor’s degree in Life Sciences or equivalent, or a qualified RN.
• Eligible to work in United States without visa sponsorship.
• 2+ years of on-site monitoring experience in pharmaceutical or CRO industry.
• Experience monitoring across multiple therapeutic areas.
• Proficient in ICH-GCP, local regulatory requirements, CTMS and eTMF.
• Clear communicator, problem-solver and collaborative team player.
• Willing to travel 60–75% for on-site monitoring across the southeast region; Orlando preferred.

Responsabilidades

• Serve as the primary point of contact between investigational sites and sponsor.
• Conduct site visits including selection, initiation, routine monitoring and close-out.
• Ensure site compliance with ICH-GCP and regulations.
• Maintain documentation in CTMS and eTMF systems.
• Support site staff training and compliance records.
• Monitor patient safety with timely AE/SAE/PQC reporting.
• Support site recruitment and retention at the site level.
• Oversee drug accountability, storage, return or destruction.
• Resolve data queries and ensure high-quality data entry.
• Document site progress and escalate risks to the clinical team.
• Assist in tracking site budgets and payments.

Conocimientos

On-site monitoring experience

Clinical trial coordination

ICH-GCP knowledge

Travel readiness 60-75%

Educación

Bachelor’s degree in Life Sciences or RN

Herramientas

CTMS

eTMF

Descripción del empleo

ICON Strategic Solutions in Orlando, FL is seeking a Clinical Research Associate to support site monitoring across multiple therapeutic areas. You will ensure regulatory compliance, maintain CTMS/eTMF documentation and drive safe, timely data entry while coordinating with sponsor teams.

The ideal candidate has 2+ years of on-site monitoring experience, a Life Sciences degree or RN, and is willing to travel up to 75% across the southeast region. Visa sponsorship is not provided.