Senior Clinical Research Associate — Cross-Therapy Trials (FL)

ICON Strategic Solutions; Florida; On-site; USD 100,000 - 130,000; Full time

Job summary

ICON Strategic Solutions is seeking a Senior Clinical Research Associate for the Florida region. The role involves on-site monitoring, site qualification, initiation, and routine monitoring to ensure data quality and patient safety.

The candidate will manage CTMS/eTMF documentation, support site staff training, and travel up to 60–75% across the southeast region. A Life Sciences degree or RN and 3+ years of on-site monitoring experience are required.

Qualifications

• Bachelor's degree in Life Sciences or RN required.
• 3+ years on-site monitoring experience in pharmaceutical or CRO settings.
• Willingness to travel up to 60–75% across southeast region; Florida residency preferred.

Responsibilities

• Serve as primary contact between investigational sites and sponsor.
• Conduct site visits: selection, initiation, routine monitoring, and close-out.
• Ensure site compliance with ICH-GCP, SOPs, and regulations.
• Maintain up-to-date CTMS and eTMF documentation.
• Support site staff training and maintain compliance records.
• Monitor patient safety and timely AE/SAE/PQC reporting.
• Support subject recruitment and retention at the site.
• Oversee drug accountability and storage/destruction as required.
• Resolve data queries and drive high-quality data entry.
• Document site progress and escalate risks to the clinical team.
• Assist in tracking site budgets and payments.
• Collaborate with CTAs, LTMs, and CTMs.

Skills

On-site monitoring

ICH-GCP

CTMS

eTMF

Cross-therapeutic areas

Travel readiness

Communication

Education

Bachelor's degree in Life Sciences or RN

Tools

CTMS

eTMF

Job description

ICON Strategic Solutions is seeking a Senior Clinical Research Associate for the Florida region. The role involves on-site monitoring, site qualification, initiation, and routine monitoring to ensure data quality and patient safety.

The candidate will manage CTMS/eTMF documentation, support site staff training, and travel up to 60–75% across the southeast region. A Life Sciences degree or RN and 3+ years of on-site monitoring experience are required.