Clinical Research Coordinator

The role

The Clinical Research Coordinator I supports and performs routine clinical research activities under the guidance of a CRC II or CRC III. This role involves coordinating low- to moderate-complexity trials and conducting participant visits.

What you will do

• Independently coordinate low- to moderate-complexity trials
• Serve as secondary CRC on high-enrolling screening trials
• Conduct participant visits including medical/psychiatric history collection, vitals, ECGs, phlebotomy, and specimen processing
• Prepare and maintain study source documents, lab kits, CRFs, and visit materials
• Ensure accurate, ALCOA+-compliant documentation and maintain required logs, trackers, and regulatory files
• Support investigational product accountability including receipt, storage, dispensing, reconciliation, and temperature monitoring
• Communicate with participants between visits
• Assist with sponsor communication, monitoring visit preparation, and audit readiness
• Contribute to query resolution, data cleaning, and study metrics tracking
• Support screening operations and meet enrollment expectations

Required qualifications

• Bachelor’s degree or equivalent years of experience in clinical trials
• At least 6 months of prior clinical research experience
• Experience running clinical trial visits
• Currently trained or willing to be trained on phlebotomy
• Strong organizational skills and ability to multitask in a fast-paced environment
• Willingness to continue learning hands-on clinical and research skills

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 focused on late-phase, industry-sponsored trials for psychiatric and neurological conditions. The organization aims to deliver data quality, safety, and diverse enrollment to advance healthcare.