Site-Based Clinical Research Associate – Travel-Ready

Bristol Myers Squibb; Columbus (OH); On-site; USD 105,000 - 127,000; Full time

Benefits offered by this job

Flexible Time Off

11 paid holidays

Wellbeing support

Job summary

Bristol Myers Squibb in Columbus, Ohio, is seeking a Clinical Research Associate to monitor clinical trial sites, ensure protocol adherence, data integrity, and regulatory compliance across study phases.

You will work with internal teams and external partners, conduct site visits, support audits, and help train site staff while focusing on patient safety and high-quality data. Travel up to 70% may be required.

Qualifications

• Bachelor’s degree in life sciences or equivalent required.
• 2-3 years of relevant clinical research experience, able to work independently.
• Experience in Pharma/Biotech or as a clinical study coordinator preferred.

Responsibilities

• Conduct site qualification, initiation, routine monitoring and close-out visits per monitoring plan.
• Verify data accuracy in electronic and paper records to ensure data integrity.
• Monitor site adherence to ICH GCP and local regulations; support audits and inspections.

Skills

ICH/GCP

Data integrity

Regulatory compliance

CTMS/eDC/eTMF

Communication

Site monitoring

Travel up to 70%

Microsoft Office

Education

Bachelor’s degree in life sciences

Tools

CTMS

eTMF

eDC

RBQM dashboards

Microsoft Office

Job description

Bristol Myers Squibb in Columbus, Ohio, is seeking a Clinical Research Associate to monitor clinical trial sites, ensure protocol adherence, data integrity, and regulatory compliance across study phases.

You will work with internal teams and external partners, conduct site visits, support audits, and help train site staff while focusing on patient safety and high-quality data. Travel up to 70% may be required.