Senior CRA, Oncology Trials — 60% Travel

ICON Strategic Solutions; New York (NY); On-site; USD 110,520 - 138,150; Full time

Benefits offered by this job

Health insurance

Retirement plan

Life assurance

Global EAP

Flexible benefits

Job summary

ICON plc, a world‑leading healthcare intelligence and clinical research organization, is seeking a Senior CRA for the NorthEast region in the United States. You will oversee monitoring of clinical trial sites, ensure adherence to protocol, GCP, and regulatory requirements, and support cross‑functional teams to drive data quality and trial progression.

The role requires extensive CRA experience, ability to manage multiple sites, and travel up to 60%.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare field.
• Extensive experience as a Clinical Research Associate.
• Ability to manage multiple sites and projects.
• Expertise in monitoring, data integrity, and site management.
• Excellent communication and stakeholder management.
• Willingness to travel ~60%.

Responsibilities

• Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and GCP.
• Conduct site visits to assess performance, resolve issues, and support successful trials.
• Collaborate with cross-functional teams to ensure timely data collection and reporting.
• Provide training and guidance to site staff and other CRAs to maintain high standards.
• Build and maintain relationships with site personnel and stakeholders to facilitate smooth operations.

Skills

Clinical trial monitoring

Site management

Regulatory compliance

GCP familiarity

Data integrity

Stakeholder management

Travel readiness

Education

Bachelor's degree in a relevant scientific discipline or healthcare-related field

Tools

Clinical trial software

Job description

ICON plc, a world‑leading healthcare intelligence and clinical research organization, is seeking a Senior CRA for the NorthEast region in the United States. You will oversee monitoring of clinical trial sites, ensure adherence to protocol, GCP, and regulatory requirements, and support cross‑functional teams to drive data quality and trial progression.

The role requires extensive CRA experience, ability to manage multiple sites, and travel up to 60%.