Senior Oncology CRA - Midwest US (60% Travel)

Regulatory Jobs; Ohio; On-site; USD 111,000 - 138,000; Full time

Benefits offered by this job

Salary base

Health & wellbeing benefits

Retirement plan

Life & disability coverage

Employee assistance programs

Learning & development

Job summary

ICON Strategic Solutions is seeking a Senior Clinical Research Associate (Oncology) for the Midwest US to oversee monitoring at sponsor sites and ensure adherence to protocol, GCP, and regulatory standards.

The role requires extensive CRA experience, ability to manage multiple sites, strong data integrity focus, and travel about 60%. Bachelor's degree in a scientific field is required, with oncology monitoring experience preferred.

Qualifications

• Experience in monitoring clinical trials and ensuring compliance with protocol, GCP, and regulatory standards.
• Ability to manage multiple sites and projects concurrently with strong organizational skills.
• Proven track record in data integrity, site management and issue resolution.
• Excellent communication and stakeholder management across cross-functional teams.
• Oncology monitoring experience and willingness to travel approximately 60%.

Responsibilities

• Lead clinical trial monitoring activities with a focus on quality and continuous improvement.
• Monitor sites for protocol compliance, regulatory adherence, and GCP standards.
• Conduct site visits to assess performance, address issues, and support trial execution.
• 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 conduct standards.

Skills

Clinical trial monitoring

Data integrity

Project management

Communication skills

Stakeholder management

Travel readiness

Education

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

Tools

Clinical trial software

Job description

ICON Strategic Solutions is seeking a Senior Clinical Research Associate (Oncology) for the Midwest US to oversee monitoring at sponsor sites and ensure adherence to protocol, GCP, and regulatory standards.

The role requires extensive CRA experience, ability to manage multiple sites, strong data integrity focus, and travel about 60%. Bachelor's degree in a scientific field is required, with oncology monitoring experience preferred.