Clinical Research Coordinator II

The role

The Clinical Research Coordinator II independently manages a portfolio of complex or high-enrolling clinical trials. This role involves leading study execution, conducting participant visits, and supervising CRC Is or RAs.

What you will do

• Manage a portfolio of complex and/or high-volume trials.
• Own study execution including screening operations and enrollment progress.
• Conduct participant visits, clinical procedures, and eligibility assessments.
• Lead study start-up activities including SIV preparation and regulatory readiness.
• Serve as the primary liaison with study sponsors, monitors, and CROs.
• Review source and eligibility criteria.
• Train and supervise CRC I's or RA's.
• Lead data entry and query resolution efforts.
• Maintain investigational product accountability.
• Identify operational risks and propose corrective actions.

Required qualifications

• Bachelor’s degree required.
• At least 1 year of prior experience as a clinical research coordinator on industry-sponsored trials.
• Demonstrated ability to manage complex studies independently.
• Comfortable with seeing 12-20 participant visits per day.
• Strong communication skills and comfort interacting directly with sponsors.

Nice to have

• Experience with neuro and/or psych patient populations a plus

Benefits

• 401(k) matching
• Medical, Dental, & Vision insurance
• Employee assistance program
• Flexible spending account
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Parental leave
• Professional development assistance

Before you apply

• Provide documentation verifying identity and authorization to work in the United States.
• Complete Form I-9 within the required timeframe.

About the company

Adams Clinical is a clinical trial site network specializing in late-phase industry-sponsored clinical research trials for psychiatric and neurological conditions. The organization focuses on delivering data quality, safety, and diverse enrollment.