Senior Oncology CRA - Midwest (60% Travel)

ICON Strategic Solutions; Indiana; On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Global Employee Assistance Programme (

Life assurance

Job summary

ICON Strategic Solutions seeks a Senior CRA (Oncology) in the US Midwest to oversee and monitor clinical trials in a sponsor-dedicated model. You will ensure protocols, regulatory requirements, and GCP standards are followed while leading site visits and continuous improvement efforts.

You will train and guide site staff, collaborate with cross-functional teams on data collection and reporting, and manage multiple sites with strong organizational skills. Willingness to travel ~60% is required.

Qualifications

• Bachelor's degree in a scientific discipline or healthcare field.
• Extensive experience as a CRA with strong regulatory knowledge.
• Proven ability to manage multiple sites and projects.
• Expertise in monitoring practices and data integrity.
• Excellent communication and stakeholder management.
• Oncology monitoring experience is required.
• Willingness to travel ~60%.
• Location: US Midwest.

Responsibilities

• Lead clinical trial monitoring tasks with emphasis on quality and continuous improvement.
• Monitor sites for protocol adherence, regulatory compliance and GCP.
• Conduct site visits to assess performance and resolve issues.
• Collaborate with cross-functional teams for timely data collection and reporting.
• Provide training and guidance to site staff and CRAs.
• Build and maintain relationships with site personnel and stakeholders.

Skills

Oncology monitoring

Clinical Research Associate

GCP knowledge

Data integrity

Site management

Travel 60%

Communication

Education

Bachelor's degree in a scientific discipline

Tools

EDC systems

CTMS

Medidata Rave

Job description

ICON Strategic Solutions seeks a Senior CRA (Oncology) in the US Midwest to oversee and monitor clinical trials in a sponsor-dedicated model. You will ensure protocols, regulatory requirements, and GCP standards are followed while leading site visits and continuous improvement efforts.

You will train and guide site staff, collaborate with cross-functional teams on data collection and reporting, and manage multiple sites with strong organizational skills. Willingness to travel ~60% is required.